DNAFORM Search Engine

参考文献: MSX1

Cunha AS, Dos Santos LV, Maran-Vsquez GA, Kirschneck C, Gerber JT, Stuani MB, Matsumoto MAN, Vieira AR, Scariot R, Kchler EC. Genetic variants in tooth agenesis-related genes might be also involved in tooth size variations. Clin Oral Investig. 2020 Jul 9. doi
Eppich S, Kuhn C, Schmoeckel E, Mayr D, Mahner S, Jeschke U, Gallwas J, Heidegger HH. MSX1-A Potential Marker for Uterus-Preserving Therapy of Endometrial Carcinomas. Int J Mol Sci. 2020 Jun 25;21(12). pii
Onizuka S, Yamazaki Y, Park SJ, Sugimoto T, Sone Y, Sjqvist S, Usui M, Takeda A, Nakai K, Nakashima K, Iwata T. RNA-sequencing reveals positional memory of multipotent mesenchymal stromal cells from oral and maxillofacial tissue transcriptomes. BMC Genomics. 2020 Jun 22;21(1):417. doi: 10.1186/s12864-020-06825-2. PubMed
Nakatomi M, Ludwig KU, Knapp M, Kist R, Lisgo S, Ohshima H, Mangold E, Peters H. Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development. Development. 2020 Jun 24;147(21). pii
Dash S, Trainor PA. The development, patterning and evolution of neural crest cell differentiation into cartilage and bone. Bone. 2020 Aug;137:115409. doi: 10.1016/j.bone.2020.115409. Epub 2020 May 14. Review. PubMed
Olsson B, Calixto RD, Machado NCS, Meger MN, Paula-Silva FWG, Rebellato NLB, Costa DJ, Kchler EC, Scariot R. MSX1 is differentially expressed in the deepest impacted maxillary third molars. Br J Oral Maxillofac Surg. 2020 May 4. pii: S0266-4356(20)30156-X. doi
Maier V, Hll M, Dietze R, Mecha EO, Omwandho COA, Tinneberg HR, Meinhold-Heerlein I, Konrad L. Adenomyotic glands are highly related to endometrial glands. Reprod Biomed Online. 2020 Jun;40(6):769-778. doi: 10.1016/j.rbmo.2019.11.007. Epub 2019 Nov 29. PubMed
Li TF, Zeng HJ, Shan Z, Ye RY, Cheang TY, Zhang YJ, Lu SH, Zhang Q, Shao N, Lin Y. Overexpression of kinesin superfamily members as prognostic biomarkers of breast cancer. Cancer Cell Int. 2020 Apr 15;20:123. doi: 10.1186/s12935-020-01191-1. eCollection 2020. PubMed
Morris VE, Hashmi SS, Zhu L, Maili L, Urbina C, Blackwell S, Greives MR, Buchanan EP, Mulliken JB, Blanton SH, Zheng WJ, Hecht JT, Letra A. Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate. Hum Genet. 2020 Apr 21. doi
Rodrigues AS, Teixeira EC, Antunes LS, Nelson-Filho P, Cunha AS, Levy SC, de Souza Arajo MT, de Carvalho Ramos AG, Cruz GV, Omori MA, Matsumoto MAN, Vieira AR, Kchler EC, Maran-Vsquez GA, Antunes LAA. Association between craniofacial morphological patterns and tooth agenesis-related genes. Prog Orthod. 2020 Apr 6;21(1):9. doi
Churchman SM, Jones EA, Roshdy T, Cox G, Boxall SA, McGonagle D, Giannoudis PV. Transient Existence of Circulating Mesenchymal Stem Cells in the Deep Veins in Humans Following Long Bone Intramedullary Reaming. J Clin Med. 2020 Mar 31;9(4). pii
Benrick A, Pillon NJ, Nilsson E, Lindgren E, Krook A, Ling C, Stener-Victorin E. Electroacupuncture Mimics Exercise-Induced Changes in Skeletal Muscle Gene Expression in Women With Polycystic Ovary Syndrome. J Clin Endocrinol Metab. 2020 Jun 1;105(6). pii
Ichihara A, Yasue A, Mitsui SN, Arai D, Minegishi Y, Oyadomari S, Imoto I, Tanaka E. The C-terminal region including the MH6 domain of Msx1 regulates skeletal development. Biochem Biophys Res Commun. 2020 May 21;526(1):62-69. doi
Griffiths RM, Pru CA, Behura SK, Cronrath AR, McCallum ML, Kelp NC, Winuthayanon W, Spencer TE, Pru JK. AMPK is required for uterine receptivity and normal responses to steroid hormones. Reproduction. 2020 May;159(6):707-717. doi: 10.1530/REP-19-0402. PubMed
Suzuki Y, Nakajima A, Kawato T, Iwata K, Motoyoshi M, Shuler CF. Identification of Smad-dependent and -independent signaling with transforming growth factor-β type 1/2 receptor inhibition in palatogenesis. J Oral Biol Craniofac Res. 2020 Apr-Jun;10(2):43-48. doi
Yao J, Qing TS, Wei X, Peng Y, Dong DX. A genome-wide association study of reproduction traits in four pig populations with different genetic backgrounds. Asian-Australas J Anim Sci. 2019 Oct 21. doi
Huang CY, Liao KW, Chou CH, Shrestha S, Yang CD, Chiew MY, Huang HT, Hong HC, Huang SH, Chang TH, Huang HD. Pilot Study to Establish a Novel Five-Gene Biomarker Panel for Predicting Lymph Node Metastasis in Patients With Early Stage Endometrial Cancer. Front Oncol. 2020 Jan 21;9:1508. doi: 10.3389/fonc.2019.01508. eCollection 2019. PubMed
Zhao M, Wang Y, Li G, Li J, Yang K, Liu C, Wen X, Song J. The role and potential mechanism of p75NTR in mineralization via in vivo p75NTR knockout mice and in vitro ectomesenchymal stem cells. Cell Prolif. 2020 Feb;53(2):e12758. doi: 10.1111/cpr.12758. Epub 2020 Jan 10. PubMed
Yang L, Liang J, Yue H, Bian Z. Two novel mutations in MSX1 causing oligodontia. PLoS One. 2020 Jan 8;15(1):e0227287. doi: 10.1371/journal.pone.0227287. eCollection 2020. PubMed
Gawron-Jakubek W, Spaczynska J, Pitynski K, Loster BW. Coexistence of tooth agenesis and ovarian cancer - a systematic literature review. Ginekol Pol. 2019;90(12):707-710. doi
Horazna M, Janeckova L, Svec J, Babosova O, Hrckulak D, Vojtechova M, Galuskova K, Sloncova E, Kolar M, Strnad H, Korinek V. Author Correction
Mártha K, Kerekes Máthé B, Moldovan VG, Bănescu C. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia. Biomed Res Int. 2019 Nov 5;2019:2183720. doi
Nagel S, Drexler HG. Deregulated NKL Homeobox Genes in B-Cell Lymphoma. Cancers (Basel). 2019 Nov 26;11(12). pii
Dalle Carbonare L, Mottes M, Cheri S, Deiana M, Zamboni F, Gabbiani D, Schena F, Salvagno GL, Lippi G, Valenti MT. Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity. Oxid Med Cell Longev. 2019 Oct 15;2019:8426259. doi: 10.1155/2019/8426259. eCollection 2019. PubMed
Crdova-Palomera A, Priest JR. Association between the 4p16 genomic locus and different types of congenital heart disease
Lancia M, Machado RA, Dionsio TJ, Garib DG, Santos CFD, Coletta RD, Neves LTD. Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis. Arch Oral Biol. 2020 Jan;109:104556. doi
Wakamatsu Y, Egawa S, Terashita Y, Kawasaki H, Tamura K, Suzuki K. Homeobox code model of heterodont tooth in mammals revised. Sci Rep. 2019 Sep 6;9(1):12865. doi
Testori A, Lasorsa VA, Cimmino F, Cantalupo S, Cardinale A, Avitabile M, Limongelli G, Russo MG, Diskin S, Maris J, Devoto M, Keavney B, Cordell HJ, Iolascon A, Capasso M. Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions
Ma T, Liu Y, Zhao X, Wu J, Wang H, Chen J, Liu P, Zhang X, Zhang X. A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia. Ann Hum Genet. 2020 Jan;84(1):97-101. doi: 10.1111/ahg.12348. Epub 2019 Aug 30. PubMed
Chen HT, Pham TV, Lin MC. Computational Study on the Mechanisms and Rate Constants for the O((3)P,(1)D) + OCS Reactions. J Phys Chem A. 2019 Oct 3;123(39):8358-8364. doi
Shibano M, Watanabe A, Takano N, Mishima H, Kinoshita A, Yoshiura KI, Shibahara T. Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population. Cleft Palate Craniofac J. 2020 Jan;57(1):80-87. doi
Suzuki A, Li A, Gajera M, Abdallah N, Zhang M, Zhao Z, Iwata J. MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells. BMC Med Genomics. 2019 Jul 1;12(1):93. doi
Chen X, Liu J, Li N, Wang Y, Zhou N, Zhu L, Shi Y, Wu Y, Xiao J, Liu C. Mesenchymal Wnt/β-catenin signaling induces Wnt and BMP antagonists in dental epithelium. Organogenesis. 2019;15(2):55-67. doi
Yu B, Jin Y, Shen Y, Yang Y, Wang G, Zhu H, Yu Y, Wang J. Loss of homeoprotein Msx1 and Msx2 leading to athletic and kinematic impairment related to the increasing neural excitability of neurons in aberrant neocortex in mice. Biochem Biophys Res Commun. 2019 Aug 13;516(1):229-235. doi: 10.1016/j.bbrc.2019.05.170. Epub 2019 Jun 17. PubMed
Amato LGL, Montenegro LR, Lerario AM, Jorge AAL, Guerra Junior G, Schnoll C, Renck AC, Trarbach EB, Costa EMF, Mendonca BB, Latronico AC, Silveira LFG. New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism. Eur J Endocrinol. 2019 Aug 1;181(2):103-119. doi
Vargas-Romero F, Gonzlez-Barrios R, Guerra-Calderas L, Escobedo-Avila I, Corts-Prez D, Lpez-Ornelas A, Rocha L, Soto-Reyes E, Velasco I. Histamine Modulates Midbrain Dopamine Neuron Differentiation Through the Regulation of Epigenetic Marks. Front Cell Neurosci. 2019 May 21;13:215. doi: 10.3389/fncel.2019.00215. eCollection 2019. PubMed
Nagel S, Pommerenke C, MacLeod RAF, Meyer C, Kaufmann M, Fhnrich S, Drexler HG. Deregulated expression of NKL homeobox genes in T-cell lymphomas. Oncotarget. 2019 May 14;10(35):3227-3247. doi
Nagel S, Uphoff CC, Dirks WG, Pommerenke C, Meyer C, Drexler HG. Epstein-Barr virus (EBV) activates NKL homeobox gene HLX in DLBCL. PLoS One. 2019 May 29;14(5):e0216898. doi
Tasanarong P, Pabalan N, Tharabenjasin P, Jarjanazi H. MSX1 gene polymorphisms and non-syndromic cleft lip with or without palate (NSCL/P)
Nettersheim D, Vadder S, Jostes S, Heimsoeth A, Schorle H. TCam-2 Cells Deficient for SOX2 and FOXA2 Are Blocked in Differentiation and Maintain a Seminoma-Like Cell Fate In Vivo. Cancers (Basel). 2019 May 25;11(5). pii
Nallasamy S, Kaya Okur HS, Bhurke A, Davila J, Li Q, Young SL, Taylor RN, Bagchi MK, Bagchi IC. Msx Homeobox Genes Act Downstream of BMP2 to Regulate Endometrial Decidualization in Mice and in Humans. Endocrinology. 2019 Jul 1;160(7):1631-1644. doi
Jiao YH, Liu M, Wang G, Li HY, Liu JS, Yang X, Yang WD. EMT is the major target for okadaic acid-suppressed the development of neural crest cells in chick embryo. Ecotoxicol Environ Saf. 2019 Sep 30;180:192-201. doi: 10.1016/j.ecoenv.2019.05.015. Epub 2019 May 11. PubMed
Grahofer A, Letko A, Hfliger IM, Jagannathan V, Ducos A, Richard O, Peter V, Nathues H, Drgemller C. Chromosomal imbalance in pigs showing a syndromic form of cleft palate. BMC Genomics. 2019 May 8;20(1):349. doi: 10.1186/s12864-019-5711-4. PubMed
Devi MSA, Padmanabhan S. Role of polymorphisms of MSX1 and PAX9 genes in palatal impaction of maxillary canines. J Orthod. 2019 Mar;46(1):14-19. doi: 10.1177/1465312518820537. Epub 2019 Jan 23. PubMed
Ma Z, Shi H, Shen Y, Li H, Yang Y, Yang J, Zhao H, Wang G, Wang J. Emerin anchors Msx1 and its protein partners at the nuclear periphery to inhibit myogenesis. Cell Biosci. 2019 Apr 11;9:34. doi
Hashimoto K, Yamaguchi Y, Kishi Y, Kikko Y, Takasaki K, Maeda Y, Matsumoto Y, Oka M, Miura M, Ohata S, Katada T, Kontani K. Loss of the small GTPase Arl8b results in abnormal development of the roof plate in mouse embryos. Genes Cells. 2019 Jun;24(6):436-448. doi
Ghazale H, Ripoll C, Leventoux N, Jacob L, Azar S, Mamaeva D, Glasson Y, Calvo CF, Thomas JL, Meneceur S, Lallemand Y, Rigau V, Perrin FE, Noristani HN, Rocamonde B, Huillard E, Bauchet L, Hugnot JP. RNA Profiling of the Human and Mouse Spinal Cord Stem Cell Niches Reveals an Embryonic-like Regionalization with MSX1(+) Roof-Plate-Derived Cells. Stem Cell Reports. 2019 May 14;12(5):1159-1177. doi
Trejo-Remigio DA, Jacinto-Alemn LF, Leyva-Huerta ER, Navarro-Bustos BR, Portilla-Robertson J. Ectodermal and ectomesenchymal marker expression in primary cell lines of complex and compound odontomas
Zhu X, Li M, Jia X, Hou W, Yang J, Zhao H, Wang G, Wang J. The homeoprotein Msx1 cooperates with Pkn1 to prevent terminal differentiation in myogenic precursor cells. Biochimie. 2019 Jul;162:55-65. doi: 10.1016/j.biochi.2019.04.003. Epub 2019 Apr 6. PubMed
Shimomura T, Kawakami M, Tatsumi K, Tanaka T, Morita-Takemura S, Kirita T, Wanaka A. The Role of the Wnt Signaling Pathway in Upper Jaw Development of Chick Embryo. Acta Histochem Cytochem. 2019 Feb 28;52(1):19-26. doi
Otsuki L, Brand AH. Dorsal-Ventral Differences in Neural Stem Cell Quiescence Are Induced by p57(KIP2)/Dacapo. Dev Cell. 2019 Apr 22;49(2):293-300.e3. doi: 10.1016/j.devcel.2019.02.015. Epub 2019 Mar 21. PubMed
Liu Z, Li C, Xu J, Lan Y, Liu H, Li X, Maire P, Wang X, Jiang R. Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial Development. J Dent Res. 2019 May;98(5):572-579. doi
Eiselleova L, Lukjanov V, Farkas S, Svoboda D, Stepka K, Koutna I. The Role of RNA Polymerase II Contiguity and Long-Range Interactions in the Regulation of Gene Expression in Human Pluripotent Stem Cells. Stem Cells Int. 2019 Feb 3;2019:1375807. doi
Balaguer N, Moreno I, Herrero M, Gonzlz-Monfort M, Vilella F, Simn C. MicroRNA-30d deficiency during preconception affects endometrial receptivity by decreasing implantation rates and impairing fetal growth. Am J Obstet Gynecol. 2019 Jul;221(1):46.e1-46.e16. doi
Koskinen S, Keski-Filppula R, Alapulli H, Nieminen P, Anttonen V. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation. Clin Oral Investig. 2019 Nov;23(11):4107-4111. doi: 10.1007/s00784-019-02849-5. Epub 2019 Feb 26. PubMed
Paccola Mesquita FC, Hochman-Mendez C, Morrissey J, Sampaio LC, Taylor DA. Laminin as a Potent Substrate for Large-Scale Expansion of Human Induced Pluripotent Stem Cells in a Closed Cell Expansion System. Stem Cells Int. 2019 Jan 22;2019:9704945. doi
Horazna M, Janeckova L, Svec J, Babosova O, Hrckulak D, Vojtechova M, Galuskova K, Sloncova E, Kolar M, Strnad H, Korinek V. Msx1 loss suppresses formation of the ectopic crypts developed in the Apc-deficient small intestinal epithelium. Sci Rep. 2019 Feb 7;9(1):1629. doi
Huguet G, Temel Y, Kdr E, Pol S, Casaca-Carreira J, Segura-Torres P, Jahanshahi A. Altered expression of dopaminergic cell fate regulating genes prior to manifestation of symptoms in a transgenic rat model of Huntington's disease. Brain Res. 2019 Jun 1;1712:101-108. doi
Xu J, Liu H, Yang Y, Wang X, Liu P, Li Y, Meyers C, Banerjee NS, Wang HK, Cam M, Lu W, Chow LT, Xie X, Zhu J, Zheng ZM. Genome-Wide Profiling of Cervical RNA-Binding Proteins Identifies Human Papillomavirus Regulation of RNASEH2A Expression by Viral E7 and E2F1. mBio. 2019 Jan 29;10(1). pii
Nagel S, MacLeod RAF, Pommerenke C, Meyer C, Kaufmann M, Drexler HG. NKL homeobox gene NKX2-2 is aberrantly expressed in Hodgkin lymphoma. Oncotarget. 2018 Dec 25;9(101):37480-37496. doi
Yan Y, Zhang XT, Wang G, Cheng X, Yan Y, Fu YJ, Yang X, Jiang Z. Zika virus induces abnormal cranial osteogenesis by negatively affecting cranial neural crest development. Infect Genet Evol. 2019 Apr;69:176-189. doi: 10.1016/j.meegid.2019.01.023. Epub 2019 Jan 19. PubMed
Umair Z, Kumar S, Kim DH, Rafiq K, Kumar V, Kim S, Park JB, Lee JY, Lee U, Kim J. Ventx1.1 as a Direct Repressor of Early Neural Gene zic3 in Xenopus laevis. Mol Cells. 2018 Dec 31;41(12):1061-1071. doi: 10.14348/molcells.2018.0341. Epub 2018 Nov 26. PubMed
Li R, Chen Z, Yu Q, Weng M, Chen Z. The Function and Regulatory Network of Pax9 Gene in Palate Development. J Dent Res. 2019 Mar;98(3):277-287. doi: 10.1177/0022034518811861. Epub 2018 Dec 24. Review. PubMed
Zhou N, Li N, Liu J, Wang Y, Gao J, Wu Y, Chen X, Liu C, Xiao J. Persistent Wnt/β-catenin signaling in mouse epithelium induces the ectopic Dspp expression in cheek mesenchyme. Organogenesis. 2019;15(1):1-12. doi: 10.1080/15476278.2018.1557026. Epub 2018 Dec 20. PubMed
Mndez-Maldonado K, Vega-Lpez G, Caballero-Chacn S, Aybar MJ, Velasco I. Activation of Hes1 and Msx1 in Transgenic Mouse Embryonic Stem Cells Increases Differentiation into Neural Crest Derivatives. Int J Mol Sci. 2018 Dec 13;19(12). pii
Hattori N, Niwa T, Ishida T, Kobayashi K, Imai T, Mori A, Kimura K, Mori T, Asami Y, Ushijima T. Antibiotics suppress colon tumorigenesis through inhibition of aberrant DNA methylation in an azoxymethane and dextran sulfate sodium colitis model. Cancer Sci. 2019 Jan;110(1):147-156. doi
Indencleef K, Roosenboom J, Hoskens H, White JD, Shriver MD, Richmond S, Peeters H, Feingold E, Marazita ML, Shaffer JR, Weinberg SM, Hens G, Claes P. Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Front Genet. 2018 Oct 25;9:502. doi
Zhang Q, Yue Y, Shi B, Yuan Z. A Bibliometric Analysis of Cleft Lip and Palate-Related Publication Trends From 2000 to 2017. Cleft Palate Craniofac J. 2019 May;56(5):658-669. doi
Nagel S, MacLeod RAF, Meyer C, Kaufmann M, Drexler HG. NKL homeobox gene activities in B-cell development and lymphomas. PLoS One. 2018 Oct 11;13(10):e0205537. doi
Shokrzadeh N, Alivand MR, Abedelahi A, Hessam Shariati MB, Niknafs B. Upregulation of HB-EGF, Msx.1, and miRNA Let-7a by administration of calcitonin through mTOR and ERK1/2 pathways during a window of implantation in mice. Mol Reprod Dev. 2018 Oct;85(10):790-801. doi
Bonczek O, Bielik P, Krejčí P, Zeman T, Izakovičová-Hollá L, Šoukalová J, Vaněk J, Gerguri T, Balcar VJ, Šerý O. Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia. PLoS One. 2018 Sep 7;13(9):e0202989. doi
Xin T, Zhang T, Li Q, Yu T, Zhu Y, Yang R, Zhou Y. A novel mutation of MSX1 in oligodontia inhibitsodontogenesis of dental pulp stem cells via the ERK pathway. Stem Cell Res Ther. 2018 Aug 22;9(1):221. doi: 10.1186/s13287-018-0965-3. PubMed
Yue Y, Zhou K, Li J, Jiang S, Li C, Men H. MSX1 induces G0/G1 arrest and apoptosis by suppressing Notch signaling and is frequently methylated in cervical cancer. Onco Targets Ther. 2018 Aug 10;11:4769-4780. doi
Liang JW, Fang ZY, Huang Y, Liuyang ZY, Zhang XL, Wang JL, Wei H, Wang JZ, Wang XC, Zeng J, Liu R. Application of Weighted Gene Co-Expression Network Analysis to Explore the Key Genes in Alzheimer's Disease. J Alzheimers Dis. 2018;65(4):1353-1364. doi
Barik M, Bajpai M, Malhotra A, Samantaray JC, Dwivedi S, Das S. Genome-Wide Association Study in Craniosynostosis Condition Using Innovative Systematic Bioinformatic Analysis Tools and Techniques
Maharana SK, Schlosser G. A gene regulatory network underlying the formation of pre-placodal ectoderm in Xenopus laevis. BMC Biol. 2018 Jul 16;16(1):79. doi
Zhang WY, Xuan B, Guo YX, Zhang J. [Changes of distal-less homeobox genes 5 and Msh homeobox 1 in a rat model of bisphosphonate related osteonecrosis of the jaw]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2018 Jul 9;53(7):466-469. doi: 10.3760/cma.j.issn.1002-0098.2018.07.007. Chinese. PubMed
Yu M, Wong SW, Han D, Cai T. Genetic analysis
Al-Dujaili M, Milne TJ, Cannon RD, Farella M. Postnatal expression of chondrogenic and osteogenic regulatory factor mRNA in the rat condylar cartilage. Arch Oral Biol. 2018 Sep;93:126-132. doi
Paranjyothi MV, Kumaraswamy KL, Begum LF, Manjunath K; Litha, Basheer S. Tooth agenesis
Fournier BP, Bruneau MH, Toupenay S, Kerner S, Berdal A, Cormier-Daire V, Hadj-Rabia S, Coudert AE, de La Dure-Molla M. Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes. J Dent Res. 2018 Nov;97(12):1306-1316. doi
Pla P, Monsoro-Burq AH. The neural border
Gomez Stallons MV, Wirrig-Schwendeman EE, Fang M, Cheek JD, Alfieri CM, Hinton RB, Yutzey KE. Molecular Mechanisms of Heart Valve Development and Disease. 2016 Jun 25. In
Katoh M. Multi‑layered prevention and treatment of chronic inflammation, organ fibrosis and cancer associated with canonical WNT/β‑catenin signaling activation (Review). Int J Mol Med. 2018 Aug;42(2):713-725. doi: 10.3892/ijmm.2018.3689. Epub 2018 May 17. Review. PubMed
Vieira AR. Hypothesis-driven versus hypothesis-free approaches to the identification of genes for cleft lip and palate. Arch Oral Biol. 2018 Aug;92:88-89. doi
Kumari P, Singh SK, Raman R. TGFβ3, MSX1, and MMP3 as Candidates for NSCL±P in an Indian Population. Cleft Palate Craniofac J. 2019 Mar;56(3):363-372. doi: 10.1177/1055665618775727. Epub 2018 May 8. PubMed
Gou Y, Li J, Wu J, Gupta R, Cho I, Ho TV, Chai Y, Merrill A, Wang J, Xu J. Prmt1 regulates craniofacial bone formation upstream of Msx1. Mech Dev. 2018 Aug;152:13-20. doi
Suazo J, Santos JL, Colombo A, Pardo R. Gene-gene interaction for nonsyndromic cleft lip with or without cleft palate in Chilean case-parent trios. Arch Oral Biol. 2018 Jul;91:91-95. doi
Gu M, Zhang Y, Liu H, Liu J, Zhu D, Yang X. MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts
Fauzi NH, Ardini YD, Zainuddin Z, Lestari W. A review on non-syndromic tooth agenesis associated with PAX9 mutations. Jpn Dent Sci Rev. 2018 Feb;54(1):30-36. doi
Nagel S, Pommerenke C, Meyer C, Kaufmann M, MacLeod RAF, Drexler HG. Aberrant expression of NKL homeobox gene HLX in Hodgkin lymphoma. Oncotarget. 2018 Feb 16;9(18):14338-14353. doi
Wang J, Li W, Zheng X, Pang X, Du G. Research progress on the forkhead box C1. Oncotarget. 2017 Nov 20;9(15):12471-12478. doi
da Silva HPV, Oliveira GHM, Ururahy MAG, Bezerra JF, de Souza KSC, Bortolin RH, Luchessi AD, Silbiger VN, Lima VMGDM, Leite GCP, Brito MEF, Ribeiro EM, Gil-da-Silva-Lopes VL, de Rezende AA. Application of high-resolution array platform for genome-wide copy number variation analysis in patients with nonsyndromic cleft lip and palate. J Clin Lab Anal. 2018 Jul;32(6):e22428. doi: 10.1002/jcla.22428. Epub 2018 Mar 7. PubMed
Yue Y, Yuan Y, Li L, Fan J, Li C, Peng W, Ren G. Homeobox protein MSX1 inhibits the growth and metastasis of breast cancer cells and is frequently silenced by promoter methylation. Int J Mol Med. 2018 May;41(5):2986-2996. doi: 10.3892/ijmm.2018.3468. Epub 2018 Feb 7. PubMed
Zhang Y, Cai S, Tseng SCG, Zhu YT. Isolation and Expansion of Multipotent Progenitors from Human Trabecular Meshwork. Sci Rep. 2018 Feb 12;8(1):2814. doi
Becic T, Kero D, Vukojevic K, Mardesic S, Saraga-Babic M. Growth factors FGF8 and FGF2 and their receptor FGFR1, transcriptional factors Msx-1 and MSX-2, and apoptotic factors p19 and RIP5 participate in the early human limb development. Acta Histochem. 2018 Apr;120(3):205-214. doi
Kantaputra PN, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns JR. WNT10B mutations associated with isolated dental anomalies. Clin Genet. 2018 May;93(5):992-999. doi: 10.1111/cge.13218. Epub 2018 Mar 2. PubMed
Liu D, Schwender H, Wang M, Wang H, Wang P, Zhu H, Zhou Z, Li J, Wu T, Beaty TH. Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palate. Birth Defects Res. 2018 Mar 1;110(4):317-324. doi
Jovanovic VM, Salti A, Tilleman H, Zega K, Jukic MM, Zou H, Friedel RH, Prakash N, Blaess S, Edenhofer F, Brodski C. BMP/SMAD Pathway Promotes Neurogenesis of Midbrain Dopaminergic Neurons In Vivo and in Human Induced Pluripotent and Neural Stem Cells. J Neurosci. 2018 Feb 14;38(7):1662-1676. doi
Faio-Flores F, Smalley KSM. Get with the Program! Stemness and Reprogramming in Melanoma Metastasis. J Invest Dermatol. 2018 Jan;138(1):10-13. doi
Estars C, Hsu HT, Huang L, Jones KA. YAP repression of the WNT3 gene controls hESC differentiation along the cardiac mesoderm lineage. Genes Dev. 2017 Nov 15;31(22):2250-2263. doi
Burmenskaya OV, Bozhenko VK, Smolnikova VY, Kalinina EA, Korneeva IE, Donnikov AE, Beyk ЕP, Naumov VA, Aleksandrova NV, Borovikov PI, Trofimov DY. Transcription profile analysis of the endometrium revealed molecular markers of the personalized 'window of implantation' during in vitro fertilization. Gynecol Endocrinol. 2017;33(sup1):22-27. doi
Yuan Q, Zhao M, Tandon B, Maili L, Liu X, Zhang A, Baugh EH, Tran T, Silva RM, Hecht JT, Swindell EC, Wagner DS, Letra A. Role of WNT10A in failure of tooth development in humans and zebrafish. Mol Genet Genomic Med. 2017 Nov;5(6):730-741. doi
Shibata A, Machida J, Yamaguchi S, Kimura M, Tatematsu T, Miyachi H, Nakayama A, Shimozato K, Tokita Y. Identification of nuclear localization signals in the human homeoprotein MSX1. Biochem Cell Biol. 2018 Aug;96(4):483-489. doi: 10.1139/bcb-2017-0263. Epub 2017 Nov 20. PubMed
Feng XY, Wu XS, Wang JS, Zhang CM, Wang SL. Homeobox protein MSX-1 inhibits expression of bone morphogenetic protein 2, bone morphogenetic protein 4, and lymphoid enhancer-binding factor 1 via Wnt/β-catenin signaling to prevent differentiation of dental mesenchymal cells during the late bell stage. Eur J Oral Sci. 2018 Feb;126(1):1-12. doi
van Nistelrooij AMJ, van Marion R, van Ijcken WFJ, de Klein A, Wagner A, Biermann K, Spaander MCW, van Lanschot JJB, Dinjens WNM, Wijnhoven BPL. Germline variant in MSX1 identified in a Dutch family with clustering of Barrett's esophagus and esophageal adenocarcinoma. Fam Cancer. 2018 Jul;17(3):435-440. doi: 10.1007/s10689-017-0054-2. PubMed
Haddaji Mastouri M, De Coster P, Zaghabani A, Jammali F, Raouahi N, Ben Salem A, Saad A, Coucke P, H'mida Ben Brahim D. Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes
Xue Y, Zhu M, Qin D, Li Y, Cen X, Sun X, Lian W, Liao B. Establishment of a congenital tooth agenesis related gene MSX1 knockout human embryonic stem cell lines by CRISPR-Cas9 technology. Stem Cell Res. 2017 Oct;24:151-154. doi: 10.1016/j.scr.2017.05.008. Epub 2017 May 24. PubMed
Murakami A, Yasuhira S, Mayama H, Miura H, Maesawa C, Satoh K. Characterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis. PLoS One. 2017 Oct 12;12(10):e0186260. doi: 10.1371/journal.pone.0186260. eCollection 2017. PubMed
Zeng B, Zhao Q, Li S, Lu H, Lu J, Ma L, Zhao W, Yu D. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis. Genes (Basel). 2017 Oct 5;8(10). pii
Nagel S, Pommerenke C, Meyer C, Kaufmann M, MacLeod RAF, Drexler HG. NKL homeobox gene MSX1 acts like a tumor suppressor in NK-cell leukemia. Oncotarget. 2017 Jun 21;8(40):66815-66832. doi
Gupta P, Chaturvedi TP, Sharma V. Expressional Analysis of MSX1 (Human) Revealed its Role in Sagittal Jaw Relationship. J Clin Diagn Res. 2017 Aug;11(8):ZC71-ZC77. doi
Daw EM, Saliba C, Grech G, Camilleri S. A novel PAX9 mutation causing oligodontia. Arch Oral Biol. 2017 Dec;84:100-105. doi: 10.1016/j.archoralbio.2017.09.018. Epub 2017 Sep 25. PubMed
Kero D, Vukojevic K, Stazic P, Sundov D, Mardesic Brakus S, Saraga-Babic M. Regulation of proliferation in developing human tooth germs by MSX homeodomain proteins and cyclin-dependent kinase inhibitor p19(INK4d). Organogenesis. 2017 Oct 2;13(4):141-155. doi
Heppt MV, Wang JX, Hristova DM, Wei Z, Li L, Evans B, Beqiri M, Zaman S, Zhang J, Irmler M, Berking C, Besch R, Beckers J, Rauscher FJ 3rd, Sturm RA, Fisher DE, Herlyn M, Fukunaga-Kalabis M. MSX1-Induced Neural Crest-Like Reprogramming Promotes MelanomaProgression. J Invest Dermatol. 2018 Jan;138(1):141-149. doi
Zhang P, Wang G, Lin Z, Wu Y, Zhang J, Liu M, Lee KKH, Chuai M, Yang X. Alcohol exposure induces chick craniofacial bone defects by negatively affecting cranial neural crest development. Toxicol Lett. 2017 Nov 5;281:53-64. doi: 10.1016/j.toxlet.2017.09.010. Epub 2017 Sep 14. PubMed
Kantaputra PN, Kapoor S, Verma P, Kaewgahya M, Kawasaki K, Ohazama A, Ketudat Cairns JR. Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation. Eur J Med Genet. 2017 Dec;60(12):695-700. doi: 10.1016/j.ejmg.2017.09.005. Epub 2017 Sep 14. PubMed
Wong SW, Han D, Zhang H, Liu Y, Zhang X, Miao MZ, Wang Y, Zhao N, Zeng L, Bai B, Wang YX, Liu H, Frazier-Bowers SA, Feng H. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype. J Dent Res. 2018 Feb;97(2):155-162. doi
Hashmi B, Mammoto T, Weaver J, Ferrante T, Jiang A, Jiang E, Feliz J, Ingber DE. Mechanical induction of dentin-like differentiation by adult mouse bone marrow stromal cells using compressive scaffolds. Stem Cell Res. 2017 Oct;24:55-60. doi
Yang QQ, Wang J, Li ZY. [Differentially expressed genes between the human mandible- and ilium- derived mesenchymal cells]. Shanghai Kou Qiang Yi Xue. 2017 Apr;26(2):180-183. Chinese. PubMed
Li J, Cui Y, Xu J, Wang Q, Yang X, Li Y, Zhang X, Qiu M, Zhang Z, Zhang Z. Suppressor of Fused restraint of Hedgehog activity level is critical for osteogenic proliferation and differentiation during calvarial bone development. J Biol Chem. 2017 Sep 22;292(38):15814-15825. doi
Dey A, Farzanehfar P, Gazina EV, Aumann TD. Electrophysiological and gene expression characterization of the ontogeny of nestin-expressing cells in the adult mouse midbrain. Stem Cell Res. 2017 Aug;23:143-153. doi: 10.1016/j.scr.2017.07.001. Epub 2017 Jul 4. PubMed
Guerrero-Flores G, Bastidas-Ponce A, Collazo-Navarrete O, Guerra-Crespo M, Covarrubias L. Functional determination of the differentiation potential of ventral mesencephalic neural precursor cells during dopaminergic neurogenesis. Dev Biol. 2017 Sep 1;429(1):56-70. doi
Li Y, Zhao D, Horie T, Chen G, Bao H, Chen S, Liu W, Horie R, Liang T, Dong B, Feng Q, Tao Q, Liu X. Conserved gene regulatory module specifies lateral neural borders across bilaterians. Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):E6352-E6360. doi
Amano T, Sagai T, Seki R, Shiroishi T. Two Types of Etiological Mutation in the Limb-Specific Enhancer of Shh. G3 (Bethesda). 2017 Sep 7;7(9):2991-2998. doi: 10.1534/g3.117.044669. PubMed
Kwon HE, Jia S, Lan Y, Liu H, Jiang R. Activin and Bmp4 Signaling Converge on Wnt Activation during Odontogenesis. J Dent Res. 2017 Sep;96(10):1145-1152. doi
Wang JY, Wang CL, Wang XM, Liu FJ. Comprehensive analysis of microRNA/mRNA signature in colon adenocarcinoma. Eur Rev Med Pharmacol Sci. 2017 May;21(9):2114-2129. PubMed
Taghiyar L, Hesaraki M, Sayahpour FA, Satarian L, Hosseini S, Aghdami N, Baghaban Eslaminejad M. Msh homeobox 1 (Msx1)- and Msx2-overexpressing bone marrow-derived mesenchymal stem cells resemble blastema cells and enhance regeneration in mice. J Biol Chem. 2017 Jun 23;292(25):10520-10533. doi: 10.1074/jbc.M116.774265. Epub 2017 May 1. PubMed
Cheng X, Li H, Yan Y, Wang G, Berman Z, Chuai M, Yang X. From the Cover: Usage of Dexamethasone Increases the Risk of Cranial Neural Crest Dysplasia in the Chick Embryo. Toxicol Sci. 2017 Jul 1;158(1):36-47. doi: 10.1093/toxsci/kfx073. PubMed
Farzanehfar P, Horne MK, Aumann TD. Can Valproic Acid Regulate Neurogenesis from Nestin+ Cells in the Adult Midbrain? Neurochem Res. 2017 Aug;42(8):2127-2134. doi
Sancho A, Vandersmissen I, Craps S, Luttun A, Groll J. A new strategy to measure intercellular adhesion forces in mature cell-cell contacts. Sci Rep. 2017 Apr 10;7:46152. doi
Cheng J, Rosario G, Cohen TV, Hu J, Stewart CL. Tissue-Specific Ablation of the LIF Receptor in the Murine Uterine Epithelium Results in Implantation Failure. Endocrinology. 2017 Jun 1;158(6):1916-1928. doi
Farzanehfar P, Horne MK, Aumann TD. An investigation of gene expression in single cells derived from Nestin-expressing cells in the adult mouse midbrain in vivo. Neurosci Lett. 2017 May 1;648:34-40. doi
Hgglund AC, Jones I, Carlsson L. A novel mouse model of anterior segment dysgenesis (ASD)
Yu Y, Zuo X, He M, Gao J, Fu Y, Qin C, Meng L, Wang W, Song Y, Cheng Y, Zhou F, Chen G, Zheng X, Wang X, Liang B, Zhu Z, Fu X, Sheng Y, Hao J, Liu Z, Yan H, Mangold E, Ruczinski I, Liu J, Marazita ML, Ludwig KU, Beaty TH, Zhang X, Sun L, Bian Z. Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. Nat Commun. 2017 Feb 24;8:14364. doi: 10.1038/ncomms14364. PubMed
Bock NC, Lenz S, Ruiz-Heiland G, Ruf S. Nonsyndromic oligodontia
Ding K, Liu WY, Zeng Q, Hou F, Xu JZ, Yang Z. Msx1-modulated muscle satellite cells retain a primitive state and exhibit an enhanced capacity for osteogenic differentiation. Exp Cell Res. 2017 Mar 1;352(1):84-94. doi: 10.1016/j.yexcr.2017.01.016. Epub 2017 Jan 31. PubMed
Xuan B, Yang P, Wu S, Li L, Zhang J, Zhang W. Expression of Dlx-5 and Msx-1 in Craniofacial Skeletons and Ilia of Rats Treated With Zoledronate. J Oral Maxillofac Surg. 2017 May;75(5):994.e1-994.e9. doi
Nagel S, Pommerenke C, Scherr M, Meyer C, Kaufmann M, Battmer K, MacLeod RA, Drexler HG. NKL homeobox gene activities in hematopoietic stem cells, T-cell development and T-cell leukemia. PLoS One. 2017 Feb 2;12(2):e0171164. doi: 10.1371/journal.pone.0171164. eCollection 2017. PubMed
Blanco R, Colombo A, Pardo R, Suazo J. Haplotype-based gene-gene interaction of bone morphogenetic protein 4 and interferon regulatory factor 6 in the etiology of non-syndromic cleft lip with or without cleft palate in a Chilean population. Eur J Oral Sci. 2017 Apr;125(2):102-109. doi
Frazier-Bowers SA, Vora SR. Genetic Disorders of Dental Development
Ozcan A, Acer H, Ciraci S, Gumus H, Karakukcu M, Patiroglu T, Ozdemir MA, Unal E. Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome. J Pediatr Hematol Oncol. 2017 May;39(4):e224-e226. doi
Kirac D, Eraydin F, Avcilar T, Ulucan K, zdemir F, Guney AI, Kaspar E, Keshi E, Isbir T. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth. Cell Mol Biol (Noisy-le-grand). 2016 Nov 30;62(13):78-84. doi
Jankovska I, Pilmane M, Akota I. Expression of gene proteins, interleukins and β-defensin in cleft-affected tissue. Stomatologija. 2017;19(4):103-108. PubMed
Blanger MC, Robert B, Cayouette M. Msx1-Positive Progenitors in the Retinal Ciliary Margin Give Rise to Both Neural and Non-neural Progenies in Mammals. Dev Cell. 2017 Jan 23;40(2):137-150. doi
Mossey PA, Little J, Steegers-Theunissen R, Molloy A, Peterlin B, Shaw WC, Johnson C, FitzPatrick DR, Franceschelli P, Rubini M. Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN Study. Cleft Palate Craniofac J. 2017 Nov;54(6):623-630. doi
Sun AJ, Gao HB, Liu G, Ge HF, Ke ZP, Li S. Identification of MSX1 and DCLK1 as mRNA Biomarkers for Colorectal Cancer Detection Through DNA Methylation Information. J Cell Physiol. 2017 Jul;232(7):1879-1884. doi
Abid MF, Simpson MA, Petridis C, Cobourne MT, Sharpe PT. Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene. Arch Oral Biol. 2017 Mar;75:8-13. doi: 10.1016/j.archoralbio.2016.11.018. Epub 2016 Dec 6. PubMed
Mitsui SN, Yasue A, Masuda K, Naruto T, Minegishi Y, Oyadomari S, Noji S, Imoto I, Tanaka E. Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development. Sci Rep. 2016 Dec 5;6:38398. doi
Zhang X, Chen Y, Ye Y, Wang J, Wang H, Yuan G, Lin Z, Wu Y, Zhang Y, Lin X. Wnt signaling promotes hindgut fate commitment through regulating multi-lineage genes during hESC differentiation. Cell Signal. 2017 Jan;29:12-22. doi: 10.1016/j.cellsig.2016.09.009. Epub 2016 Sep 29. PubMed
Bonic A, Poon M, Woods MG, Trounson AO. Expression of neural crest markers by human embryonic stem cells
Nishihara H, Kobayashi N, Kimura-Yoshida C, Yan K, Bormuth O, Ding Q, Nakanishi A, Sasaki T, Hirakawa M, Sumiyama K, Furuta Y, Tarabykin V, Matsuo I, Okada N. Coordinately Co-opted Multiple Transposable Elements Constitute an Enhancer for wnt5a Expression in the Mammalian Secondary Palate. PLoS Genet. 2016 Oct 14;12(10):e1006380. doi
Ibarra-Arce A, Albavera-Giles T, Zavaleta-Villa B, Ortiz de Zrate-Alarcn G, Flores-Pea L, Sierra-Romero MD, Romero-Valdovinos M, Olivo-Daz A. MSX1 gene polymorphisms in Mexican patients with non-syndromic cleft lip/palate. Int J Pediatr Otorhinolaryngol. 2016 Nov;90:119-124. doi
Jia S, Kwon HE, Lan Y, Zhou J, Liu H, Jiang R. Bmp4-Msx1 signaling and Osr2 control tooth organogenesis through antagonistic regulation of secreted Wnt antagonists. Dev Biol. 2016 Dec 1;420(1):110-119. doi: 10.1016/j.ydbio.2016.10.001. Epub 2016 Oct 3. PubMed
Phan M, Conte F, Khandelwal KD, Ockeloen CW, Bartzela T, Kleefstra T, van Bokhoven H, Rubini M, Zhou H, Carels CE. Tooth agenesis and orofacial clefting: genetic brothers in arms? Hum Genet. 2016 Dec;135(12):1299-1327. Epub 2016 Oct 3. Review. PubMed
Salvi A, Giacopuzzi E, Bardellini E, Amadori F, Ferrari L, De Petro G, Borsani G, Majorana A. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis. Int J Mol Med. 2016 Nov;38(5):1338-1348. doi
Suzuki K, Matsumaru D, Matsushita S, Murashima A, Ludwig M, Reutter H, Yamada G. Epispadias and the associated embryopathies
Goto N, Fujimoto K, Fujii S, Ida-Yonemochi H, Ohshima H, Kawamoto T, Noshiro M, Shukunami C, Kozai K, Kato Y. Role of MSX1 in Osteogenic Differentiation of Human Dental Pulp Stem Cells. Stem Cells Int. 2016;2016:8035759. doi: 10.1155/2016/8035759. Epub 2016 Aug 28. PubMed
Costamagna D, Mommaerts H, Sampaolesi M, Tylzanowski P. Noggin inactivation affects the number and differentiation potential of muscle progenitor cells in vivo. Sci Rep. 2016 Aug 30;6:31949. doi
Peng HH, Chang NC, Chen KT, Lu JJ, Chang PY, Chang SC, Wu-Chou YH, Chou YT, Phang W, Cheng PJ. Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population. BMC Med Genet. 2016 Aug 15;17(1):59. doi
Amri N, Djol SX, Petit S, Babajko S, Coudert AE, Castaneda B, Simon S, Berdal A. Distorted Patterns of Dentinogenesis and Eruption in Msx2 Null Mutants: Involvement of Sost/Sclerostin. Am J Pathol. 2016 Oct;186(10):2577-87. doi: 10.1016/j.ajpath.2016.06.013. Epub 2016 Aug 11. PubMed
Haddaji Mastouri M, De Coster P, Zaghabani A, Trabelsi S, May Y, Saad A, Coucke P, H'mida Ben Brahim D. Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis. Arch Oral Biol. 2016 Nov;71:110-116. doi
Xue J, Gao Q, Huang Y, Zhang X, Yang P, Cram DS, Liang D, Wu L. A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree. Clin Chim Acta. 2016 Oct 1;461:135-40. doi: 10.1016/j.cca.2016.07.025. Epub 2016 Jul 30. PubMed
Pengelly RJ, Arias L, Martnez J, Upstill-Goddard R, Seaby EG, Gibson J, Ennis S, Collins A, Briceo I. Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes. Sci Rep. 2016 Jul 26;6:30457. doi
Sun J, Ting MC, Ishii M, Maxson R. Msx1 and Msx2 function together in the regulation of primordial germ cell migration in the mouse. Dev Biol. 2016 Sep 1;417(1):11-24. doi
Liang J, Von den Hoff J, Lange J, Ren Y, Bian Z, Carels CE. MSX1 mutations and associated disease phenotypes
Srvri M, Kall I, Hrabovszky E, Solymosi N, Rodolosse A, Liposits Z. Long-Term Estrogen Receptor Beta Agonist Treatment Modifies the Hippocampal Transcriptome in Middle-Aged Ovariectomized Rats. Front Cell Neurosci. 2016 Jun 10;10:149. doi
Gowans LJ, Adeyemo WL, Eshete M, Mossey PA, Busch T, Aregbesola B, Donkor P, Arthur FK, Bello SA, Martinez A, Li M, Augustine-Akpan EA, Deressa W, Twumasi P, Olutayo J, Deribew M, Agbenorku P, Oti AA, Braimah R, Plange-Rhule G, Gesses M, Obiri-Yeboah S, Oseni GO, Olaitan PB, Abdur-Rahman L, Abate F, Hailu T, Gravem P, Ogunlewe MO, Bux CJ, Marazita ML, Adeyemo AA, Murray JC, Butali A. Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations. J Dent Res. 2016 Oct;95(11):1245-56. doi
Shahid M, Balto HA, Al-Hammad N, Joshi S, Khalil HS, Somily AM, Sinjilawi NA, Al-Ghamdi S, Faiyaz-Ul-Haque M, Dhillon VS. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis. Eur J Med Genet. 2016 Aug;59(8):377-85. doi
Du J, Deng J. Associations Between TGFA/TGFB3/MSX1 Gene Polymorphisms and Congenital Non-Syndromic Hearing Impairment in a Chinese Population. Med Sci Monit. 2016 Jun 29;22:2253-66. PubMed
Nagel S, Pommerenke C, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Deregulation of polycomb repressor complex 1 modifier AUTS2 in T-cell leukemia. Oncotarget. 2016 Jul 19;7(29):45398-45413. doi
Bolnick AD, Bolnick JM, Kilburn BA, Stewart T, Oakes J, Rodriguez-Kovacs J, Kohan-Ghadr HR, Dai J, Diamond MP, Hirota Y, Drewlo S, Dey SK, Armant DR; NICHD National Cooperative Reproductive Medicine Network. Reduced homeobox protein MSX1 in human endometrial tissue is linked to infertility. Hum Reprod. 2016 Sep;31(9):2042-50. doi
Parrilla M, Chang I, Degl'Innocenti A, Omura M. Expression of homeobox genes in the mouse olfactory epithelium. J Comp Neurol. 2016 Oct 1;524(14):2713-39. doi
Aslar Oner D, Tastan H. Association of MSX1 c.*6C > T Variant with Nonsyndromic Cleft Lip With or Without Cleft Palate in Turkish Patients. Genet Test Mol Biomarkers. 2016 Jul;20(7):402-5. doi
Wang CJ, Wang G, Wang XY, Liu M, Chuai M, Lee KK, He XS, Lu DX, Yang X. Imidacloprid Exposure Suppresses Neural Crest Cells Generation during Early Chick Embryo Development. J Agric Food Chem. 2016 Jun 15;64(23):4705-15. doi: 10.1021/acs.jafc.6b01478. Epub 2016 Jun 1. PubMed
Chen LT, Hu MM, Xu ZS, Liu Y, Shu HB. MSX1 Modulates RLR-Mediated Innate Antiviral Signaling by Facilitating Assembly of TBK1-Associated Complexes. J Immunol. 2016 Jul 1;197(1):199-207. doi
Yue H, Liang J, Yang K, Hua B, Bian Z. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis. Eur J Oral Sci. 2016 Jun;124(3):228-33. doi
Gaczkowska A, Abdalla EM, Dowidar KM, Elhady GM, Jagodzinski PP, Mostowska A. De novo EDA mutations
Zhao MY, Yu Y, Xie M, Yang MH, Zhu S, Yang LC, Kang R, Tang DL, Zhao LL, Cao LZ. Digital gene expression profiling analysis of childhood acute lymphoblastic leukemia. Mol Med Rep. 2016 May;13(5):4321-8. doi
Zheng Y, Cai J, Hutchins AP, Jia L, Liu P, Yang D, Chen S, Ge L, Pei D, Wei S. Remission for Loss of Odontogenic Potential in a New Micromilieu In Vitro. PLoS One. 2016 Apr 6;11(4):e0152893. doi
Luan F, Sun F, Xu C, Zhang H. WITHDRAWN
Sanchez-Ferras O, Bernas G, Farnos O, Tour AM, Souchkova O, Pilon N. A direct role for murine Cdx proteins in the trunk neural crest gene regulatory network. Development. 2016 Apr 15;143(8):1363-74. doi
Mimura S, Suga M, Okada K, Kinehara M, Nikawa H, Furue MK. Bone morphogenetic protein 4 promotes craniofacial neural crest induction from human pluripotent stem cells. Int J Dev Biol. 2016;60(1-3):21-8. doi: 10.1387/ijdb.160040mk. PubMed
Trujillo-Paredes N, Valencia C, Guerrero-Flores G, Arzate DM, Baizabal JM, Guerra-Crespo M, Fuentes-Hernndez A, Zea-Armenta I, Covarrubias L. Regulation of differentiation flux by Notch signalling influences the number of dopaminergic neurons in the adult brain. Biol Open. 2016 Feb 24;5(3):336-47. doi: 10.1242/bio.013383. PubMed
Lee SI, Jang HJ, Jeon MH, Lee MO, Kim JS, Jeon IS, Byun SJ. Transcriptional regulation of cathelicidin genes in chicken bone marrow cells. Poult Sci. 2016 Apr;95(4):912-9. doi
Roellig D, Bronner ME. The epigenetic modifier DNMT3A is necessary for proper otic placode formation. Dev Biol. 2016 Mar 15;411(2):294-300. doi: 10.1016/j.ydbio.2016.01.034. Epub 2016 Jan 28. PubMed
Macr S, Simula L, Pellarin I, Pegoraro S, Onorati M, Sgarra R, Manfioletti G, Vignali R. Hmga2 is required for neural crest cell specification in Xenopus laevis. Dev Biol. 2016 Mar 1;411(1):25-37. doi
Bonito NA, Borley J, Wilhelm-Benartzi CS, Ghaem-Maghami S, Brown R. Epigenetic Regulation of the Homeobox Gene MSX1 Associates with Platinum-Resistant Disease in High-Grade Serous Epithelial Ovarian Cancer. Clin Cancer Res. 2016 Jun 15;22(12):3097-3104. doi
Wang J, Sun K, Shen Y, Xu Y, Xie J, Huang R, Zhang Y, Xu C, Zhang X, Wang R, Lin Y. DNA methylation is critical for tooth agenesis
Takechi M, Kitazawa T, Hirasawa T, Hirai T, Iseki S, Kurihara H, Kuratani S. Developmental mechanisms of the tympanic membrane in mammals and non-mammalian amniotes. Congenit Anom (Kyoto). 2016 Jan;56(1):12-7. doi
Rao J, Pfeiffer MJ, Frank S, Adachi K, Piccini I, Quaranta R, Arazo-Bravo M, Schwarz J, Schade D, Leidel S, Schler HR, Seebohm G, Greber B. Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs. Cell Stem Cell. 2016 Mar 3;18(3):341-53. doi
Hlousková A, Bonczek O, Izakovicová-Hollá L, Lochman J, Soukalová J, Stembírek J, Mísek I, Cernochová P, Krejcí P, Vanek J, Šerý O. Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population. Neuro Endocrinol Lett. 2015;36(5):452-7. PubMed
Sun X, Park CB, Deng W, Potter SS, Dey SK. Uterine inactivation of muscle segment homeobox (Msx) genes alters epithelial cell junction proteins during embryo implantation. FASEB J. 2016 Apr;30(4):1425-35. doi
Nishimura N, Ueharu H, Nishihara H, Shibuya S, Yoshida S, Higuchi M, Kanno N, Horiguchi K, Kato T, Kato Y. Search for regulatory factors of the pituitary-specific transcription factor PROP1 gene. J Reprod Dev. 2016;62(1):93-102. doi
Zhang XX, Wong SW, Han D, Feng HL. Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia. Chin J Dent Res. 2015;18(4):229-34. doi
Vojnits K, Pan H, Mu X, Li Y. Characterization of an Injury Induced Population of Muscle-Derived Stem Cell-Like Cells. Sci Rep. 2015 Nov 27;5:17355. doi
de Araujo TK, Secolin R, Flix TM, de Souza LT, Fontes M, Monlle IL, de Souza J, Fett-Conte AC, Ribeiro EM, Xavier AC, de Rezende AA, Simioni M, Ribeiro-dos-Santos K, dos Santos SE, Gil-da-Silva-Lopes VL. A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population. J Craniomaxillofac Surg. 2016 Jan;44(1):16-20. doi: 10.1016/j.jcms.2015.07.026. Epub 2015 Aug 13. PubMed
Yin W, Bian Z. Hypodontia, a prospective predictive marker for tumor? Oral Dis. 2016 May;22(4):265-73. doi
Abe S, Yamaguchi S, Sato Y, Harada K. Sphere-Derived Multipotent Progenitor Cells Obtained From Human Oral Mucosa Are Enriched in Neural Crest Cells. Stem Cells Transl Med. 2016 Jan;5(1):117-28. doi
Liang J, Qin C, Yue H, He H, Bian Z. A novel initiation codon mutation of PAX9 in a family with oligodontia. Arch Oral Biol. 2016 Jan;61:144-8. doi: 10.1016/j.archoralbio.2015.10.022. Epub 2015 Oct 30. PubMed
Li FF, Han Y, Shi S, Li X, Zhu XD, Zhou J, Shao QL, Li XQ, Liu SL. Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases. PLoS One. 2015 Nov 10;10(11):e0142666. doi
Daubas P, Duval N, Bajard L, Langa Vives F, Robert B, Mankoo BS, Buckingham M. Fine-tuning the onset of myogenesis by homeobox proteins that interact with the Myf5 limb enhancer. Biol Open. 2015 Nov 4;4(12):1614-24. doi: 10.1242/bio.014068. PubMed
Bellessort B, Le Cardinal M, Bachelot A, Narboux-Nme N, Garagnani P, Pirazzini C, Barbieri O, Mastracci L, Jonchere V, Duvernois-Berthet E, Fontaine A, Alfama G, Levi G. Dlx5 and Dlx6 control uterine adenogenesis during post-natal maturation
Park KS, Kim KK, Kim KE. Msx1 homeodomain transcription factor and TATA-binding protein interact to repress the expression of the glycoprotein hormone α subunit gene. Biochem Biophys Res Commun. 2015 Dec 4-11;468(1-2):326-30. doi
Nagel S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Aberrant expression of homeobox gene SIX1 in Hodgkin lymphoma. Oncotarget. 2015 Nov 24;6(37):40112-26. doi
Yilmaz A, Engeler R, Constantinescu S, Kokkaliaris KD, Dimitrakopoulos C, Schroeder T, Beerenwinkel N, Paro R. Ectopic expression of Msx2 in mammalian myotubes recapitulates aspects of amphibian muscle dedifferentiation. Stem Cell Res. 2015 Nov;15(3):542-553. doi
Wattanarat O, Kantaputra PN. Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations. Am J Med Genet A. 2016 Jan;170A(1):254-9. doi
Kantaputra PN, Kaewgahya M, Hatsadaloi A, Vogel P, Kawasaki K, Ohazama A, Ketudat Cairns JR. GREMLIN 2 Mutations and Dental Anomalies. J Dent Res. 2015 Dec;94(12):1646-52. doi
Nagel S, Ehrentraut S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Aberrantly Expressed OTX Homeobox Genes Deregulate B-Cell Differentiation in Hodgkin Lymphoma. PLoS One. 2015 Sep 25;10(9):e0138416. doi: 10.1371/journal.pone.0138416. eCollection 2015. PubMed
Machado RA, Messetti AC, de Aquino SN, Martelli-Jnior H, Swerts MS, de Almeida Reis SR, Moreira HS, Persuhn DC, Coletta RD. Association Between Genes Involved in Craniofacial Development and Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population. Cleft Palate Craniofac J. 2016 Sep;53(5):550-6. doi: 10.1597/15-107. Epub 2015 Sep 24. PubMed
Vandersmissen I, Craps S, Depypere M, Coppiello G, van Gastel N, Maes F, Carmeliet G, Schrooten J, Jones EA, Umans L, Devlieger R, Koole M, Gheysens O, Zwijsen A, Aranguren XL, Luttun A. Endothelial Msx1 transduces hemodynamic changes into an arteriogenic remodeling response. J Cell Biol. 2015 Sep 28;210(7):1239-56. doi
Vance KW, Woodcock DJ, Reid JE, Bretschneider T, Ott S, Koentges G. Conserved Cis-Regulatory Modules Control Robustness in Msx1 Expression at Single-Cell Resolution. Genome Biol Evol. 2015 Sep 4;7(9):2762-78. doi: 10.1093/gbe/evv179. PubMed
Tao H, Guo L, Chen L, Qiao G, Meng X, Xu B, Ye W. MSX1 inhibits cell migration and invasion through regulating the Wnt/β-catenin pathway in glioblastoma. Tumour Biol. 2016 Jan;37(1):1097-104. doi: 10.1007/s13277-015-3892-2. Epub 2015 Aug 15. PubMed
Thimmegowda U, Prasanna P, Athimuthu A, Bhat PK, Puttashamachari Y. A Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of PAX9-A Clinical and Genetic Report. J Clin Diagn Res. 2015 Jun;9(6):ZD08-10. doi: 10.7860/JCDR/2015/13173.6049. Epub 2015 Jun 1. PubMed
Simes-Costa M, Stone M, Bronner ME. Axud1 Integrates Wnt Signaling and Transcriptional Inputs to Drive Neural Crest Formation. Dev Cell. 2015 Sep 14;34(5):544-54. doi
Fujii S, Fujimoto K, Goto N, Kanawa M, Kawamoto T, Pan H, Srivatanakul P, Rakdang W, Pornprasitwech J, Saskianti T, Suardita K, Nishimura F, Kato Y. Characteristic expression of MSX1, MSX2, TBX2 and ENTPD1 in dental pulp cells. Biomed Rep. 2015 Jul;3(4):566-572. Epub 2015 Apr 29. PubMed
Seki D, Takeshita N, Oyanagi T, Sasaki S, Takano I, Hasegawa M, Takano-Yamamoto T. Differentiation of Odontoblast-Like Cells From Mouse Induced Pluripotent Stem Cells by Pax9 and Bmp4 Transfection. Stem Cells Transl Med. 2015 Sep;4(9):993-7. doi
Snowball J, Ambalavanan M, Whitsett J, Sinner D. Endodermal Wnt signaling is required for tracheal cartilage formation. Dev Biol. 2015 Sep 1;405(1):56-70. doi
Dai J, Yu H, Si J, Fang B, Shen SG. Irf6-Related Gene Regulatory Network Involved in Palate and Lip Development. J Craniofac Surg. 2015 Jul;26(5):1600-5. doi
Tatematsu T, Kimura M, Nakashima M, Machida J, Yamaguchi S, Shibata A, Goto H, Nakayama A, Higashi Y, Miyachi H, Shimozato K, Matsumoto N, Tokita Y. An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family. PLoS One. 2015 Jun 1;10(6):e0128227. doi
McCoy CR, Stadelman BS, Brumaghim JL, Liu JT, Bain LJ. Arsenic and Its Methylated Metabolites Inhibit the Differentiation of Neural Plate Border Specifier Cells. Chem Res Toxicol. 2015 Jul 20;28(7):1409-21. doi: 10.1021/acs.chemrestox.5b00036. Epub 2015 Jun 10. PubMed
Hing B, Ramos E, Braun P, McKane M, Jancic D, Tamashiro KL, Lee RS, Michaelson JJ, Druley TE, Potash JB. Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment. Epigenetics. 2015;10(7):581-96. doi
Wang T, Xu Y, Hou P. Identifying novel biomarkers of gastric cancer through integration analysis of single nucleotide polymorphisms and gene expression profile. Int J Biol Markers. 2015 Jul 22;30(3):e321-6. doi
Gurramkonda VB, Syed AH, Murthy J, Lakkakula BV. Evidence of the involvement of the polymorphisms near MSX1 gene in non-syndromic cleft lip with or without cleft palate. Int J Pediatr Otorhinolaryngol. 2015 Jul;79(7):1081-4. doi: 10.1016/j.ijporl.2015.04.034. Epub 2015 Apr 29. PubMed
Papoutsi T, Odelin G, Moore-Morris T, Pucat M, de la Pompa JL, Robert B, Zaffran S. Msx1CreERT2 knock-In allele
Cha J, Burnum-Johnson KE, Bartos A, Li Y, Baker ES, Tilton SC, Webb-Robertson BJ, Piehowski PD, Monroe ME, Jegga AG, Murata S, Hirota Y, Dey SK. Muscle Segment Homeobox Genes Direct Embryonic Diapause by Limiting Inflammation in the Uterus. J Biol Chem. 2015 Jun 12;290(24):15337-49. doi: 10.1074/jbc.M115.655001. Epub 2015 Apr 30. PubMed
Kwon HJ, Park EK, Jia S, Liu H, Lan Y, Jiang R. Deletion of Osr2 Partially Rescues Tooth Development in Runx2 Mutant Mice. J Dent Res. 2015 Aug;94(8):1113-9. doi
Yin W, Bian Z. The Gene Network Underlying Hypodontia. J Dent Res. 2015 Jul;94(7):878-85. doi
AlFawaz S, Plagnol V, Wong FS, Kelsell DP. A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis. Arch Oral Biol. 2015 Jul;60(7):982-8. doi
Ruzicka WB, Subburaju S, Benes FM. Circuit- and Diagnosis-Specific DNA Methylation Changes at γ-Aminobutyric Acid-Related Genes in Postmortem Human Hippocampus in Schizophrenia and Bipolar Disorder. JAMA Psychiatry. 2015 Jun;72(6):541-51. doi
Mao Y, Xiong L, Wang S, Zhong J, Zhou R, Li L. Comparison of the transcriptomes of mouse skin derived precursors (SKPs) and SKP-derived fibroblasts (SFBs) by RNA-Seq. PLoS One. 2015 Feb 26;10(2):e0117739. doi: 10.1371/journal.pone.0117739. eCollection 2015. PubMed
Huang Y, Yang Y, Jiang M, Lin M, Li S, Lin Y. Immortalization and characterization of human dental mesenchymal cells. J Dent. 2015 May;43(5):576-82. doi
Šerý O, Bonczek O, Hloušková A, Černochová P, Vaněk J, Míšek I, Krejčí P, Izakovičová Hollá L. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene. Eur J Oral Sci. 2015 Apr;123(2):65-71. doi
Lainoff AJ, Moustakas-Verho JE, Hu D, Kallonen A, Marcucio RS, Hlusko LJ. A comparative examination of odontogenic gene expression in both toothed and toothless amniotes. J Exp Zool B Mol Dev Evol. 2015 May;324(3):255-69. doi: 10.1002/jez.b.22594. Epub 2015 Feb 11. PubMed
Marrelli M, Paduano F, Tatullo M. Human periapical cyst-mesenchymal stem cells differentiate into neuronal cells. J Dent Res. 2015 Jun;94(6):843-52. doi
Naillat F, Yan W, Karjalainen R, Liakhovitskaia A, Samoylenko A, Xu Q, Sun Z, Shen B, Medvinsky A, Quaggin S, Vainio SJ. Identification of the genes regulated by Wnt-4, a critical signal for commitment of the ovary. Exp Cell Res. 2015 Mar 15;332(2):163-78. doi
Serra-Juh C, Cusc I, Homs A, Flores R, Torn N, Prez-Jurado LA. DNA methylation abnormalities in congenital heart disease. Epigenetics. 2015;10(2):167-77. doi
Ceyhan D, Kirzioglu Z, Calapoglu NS. Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. Indian J Dent. 2014 Oct;5(4):172-82. doi
Paradowska-Stolarz A. MSX1 gene in the etiology orofacial deformities. Postepy Hig Med Dosw (Online). 2015 Dec 31;69:1499-504. Review. PubMed PMID: 27259221.
Mostowska A, Biedziak B, Zadurska M, Matuszewska-Trojan S, Jagodziński PP. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies. Eur J Oral Sci. 2015 Feb;123(1):1-8. doi
Lieven O, Dronka J, Burmhl S, Rther U. Differential binding of Lef1 and Msx1/2 transcription factors to Dkk1 CNEs correlates with reporter gene expression in vivo. PLoS One. 2014 Dec 29;9(12):e115442. doi: 10.1371/journal.pone.0115442. eCollection 2014. PubMed
Zhang Z, Shi Y, Zhao S, Li J, Li C, Mao B. Xenopus Nkx6.3 is a neural plate border specifier required for neural crest development. PLoS One. 2014 Dec 22;9(12):e115165. doi
Kristensen SG, Ebbesen P, Andersen CY. Transcriptional profiling of five isolated size-matched stages of human preantral follicles. Mol Cell Endocrinol. 2015 Feb 5;401:189-201. doi
Zhang W, Qu HC, Zhang Y. Association of MSX1 and TGF-β1 genetic polymorphisms with hypodontia
Zandarashvili L, Iwahara J. Temperature dependence of internal motions of protein side-chain NH3(+) groups
Kachhap S, Singh B. Role of DNA conformation & energetic insights in Msx-1-DNA recognition as revealed by molecular dynamics studies on specific and nonspecific complexes. J Biomol Struct Dyn. 2015;33(10):2069-82. doi: 10.1080/07391102.2014.995709. Epub 2015 Jan 12. PubMed
Kodaka Y, Tanaka K, Kitajima K, Tanegashima K, Matsuda R, Hara T. LIM homeobox transcription factor Lhx2 inhibits skeletal muscle differentiation in part via transcriptional activation of Msx1 and Msx2. Exp Cell Res. 2015 Feb 15;331(2):309-19. doi
Yuan G, Yang G, Zheng Y, Zhu X, Chen Z, Zhang Z, Chen Y. The non-canonical BMP and Wnt/β-catenin signaling pathways orchestrate early tooth development. Development. 2015 Jan 1;142(1):128-39. doi
Belmadani S, Matrougui K. Can the NK family of osteoblast homeodomain transcription factors signaling be a magic bullet to reverse calcification-induced vasculopathy in diabetes? Diabetes. 2014 Dec;63(12):4011-2. doi
Simioni M, Araujo TK, Monlleo IL, Maurer-Morelli CV, Gil-da-Silva-Lopes VL. Investigation of genetic factors underlying typical orofacial clefts
Qin H, Cai J. Axis inhibition protein 2 polymorphisms may be a risk factor for families with isolated oligodontia. Mol Med Rep. 2015 Mar;11(3):1899-904. doi
Křivánek J, Švandová E, Králik J, Hajda Š, Fedr R, Vinarský V, Jaroš J, Souček K, Buchtová M, Matalová E, Hampl A. Properties of neural crest-like cells differentiated from human embryonic stem cells. Folia Biol (Praha). 2014;60 Suppl 1:30-8. PubMed
Lee JT, Choi SY, Kim HL, Kim JY, Lee HJ, Kwon TG. Comparison of gene expression between mandibular and iliac bone-derived cells. Clin Oral Investig. 2015 Jul;19(6):1223-33. doi
Jacques-Fricke BT, Gammill LS. Neural crest specification and migration independently require NSD3-related lysine methyltransferase activity. Mol Biol Cell. 2014 Dec 15;25(25):4174-86. doi
Yang G, Yuan G, Ye W, Cho KW, Chen Y. An atypical canonical bone morphogenetic protein (BMP) signaling pathway regulates Msh homeobox 1 (Msx1) expression during odontogenesis. J Biol Chem. 2014 Nov 7;289(45):31492-502. doi
Shimomura T, Kawakami M, Okuda H, Tatsumi K, Morita S, Nochioka K, Kirita T, Wanaka A. Retinoic acid regulates Lhx8 expression via FGF-8b to the upper jaw development of chick embryo. J Biosci Bioeng. 2015 Mar;119(3):260-6. doi: 10.1016/j.jbiosc.2014.08.010. Epub 2014 Sep 18. PubMed
Sarkar T, Bansal R, Das P. Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis. PLoS One. 2014 Sep 9;9(9):e106811. doi
Schlosser G. Early embryonic specification of vertebrate cranial placodes. Wiley Interdiscip Rev Dev Biol. 2014 Sep-Oct;3(5):349-63. doi
Svandova E, Lesot H, Vanden Berghe T, Tucker AS, Sharpe PT, Vandenabeele P, Matalova E. Non-apoptotic functions of caspase-7 during osteogenesis. Cell Death Dis. 2014 Aug 14;5:e1366. doi
De Cecco L, Negri T, Brich S, Mauro V, Bozzi F, Dagrada G, Disciglio V, Sanfilippo R, Gronchi A, D'Incalci M, Casali PG, Canevari S, Pierotti MA, Pilotti S. Identification of a gene expression driven progression pathway in myxoid liposarcoma. Oncotarget. 2014 Aug 15;5(15):5965-77. PubMed
Yamaguchi S, Machida J, Kamamoto M, Kimura M, Shibata A, Tatematsu T, Miyachi H, Higashi Y, Jezewski P, Nakayama A, Shimozato K, Tokita Y. Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis. PLoS One. 2014 Aug 7;9(8):e102944. doi: 10.1371/journal.pone.0102944. eCollection 2014. PubMed
Blanco R, Colombo A, Suazo J. Genetic risk score for nonsyndromic cleft lip with or without cleft palate for a Chilean population. Genet Couns. 2014;25(2):143-9. PubMed
Cheng SL, Behrmann A, Shao JS, Ramachandran B, Krchma K, Bello Arredondo Y, Kovacs A, Mead M, Maxson R, Towler DA. Targeted reduction of vascular Msx1 and Msx2 mitigates arteriosclerotic calcification and aortic stiffness in LDLR-deficient mice fed diabetogenic diets. Diabetes. 2014 Dec;63(12):4326-37. doi
Nagel S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Deregulated FOX genes in Hodgkin lymphoma. Genes Chromosomes Cancer. 2014 Nov;53(11):917-33. doi: 10.1002/gcc.22204. Epub 2014 Jul 17. PubMed
Paradowska-Stolarz AM. Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome. Adv Clin Exp Med. 2014 May-Jun;23(3):485-9. Review. PubMed
Nassif A, Senussi I, Meary F, Loiodice S, Hotton D, Robert B, Bensidhoum M, Berdal A, Babajko S. Msx1 role in craniofacial bone morphogenesis. Bone. 2014 Sep;66:96-104. doi
Yang Z, Liu Q, Mannix RJ, Xu X, Li H, Ma Z, Ingber DE, Allen PD, Wang Y. Mononuclear cells from dedifferentiation of mouse myotubes display remarkable regenerative capability. Stem Cells. 2014 Sep;32(9):2492-501. doi: 10.1002/stem.1742. PubMed
Wong SW, Liu HC, Han D, Chang HG, Zhao HS, Wang YX, Feng HL. A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia. Mutagenesis. 2014 Sep;29(5):319-23. doi
Yoshida S, Higuchi M, Ueharu H, Nishimura N, Tsuda M, Yako H, Chen M, Mitsuishi H, Sano Y, Kato T, Kato Y. Characterization of murine pituitary-derived cell lines Tpit/F1, Tpit/E and TtT/GF. J Reprod Dev. 2014;60(4):295-303. Epub 2014 Jun 2. PubMed
Barrio MC, Del Río A, Murillo J, Maldonado E, López-Gordillo Y, Paradas-Lara I, Hernandes L, Catón J, Martínez-Álvarez C. Epidermal growth factor impairs palatal shelf adhesion and fusion in the Tgf-β 3 null mutant. Cells Tissues Organs. 2014;199(2-3):201-11. doi
Nagel S, Ehrentraut S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Repressed BMP signaling reactivates NKL homeobox gene MSX1 in a T-ALL subset. Leuk Lymphoma. 2015 Feb;56(2):480-91. doi
Kiso H, Takahashi K, Saito K, Togo Y, Tsukamoto H, Huang B, Sugai M, Shimizu A, Tabata Y, Economides AN, Slavkin HC, Bessho K. Interactions between BMP-7 and USAG-1 (uterine sensitization-associated gene-1) regulate supernumerary organ formations. PLoS One. 2014 May 9;9(5):e96938. doi
Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family. Arch Oral Biol. 2014 Jul;59(7):722-8. doi
He F, Hu X, Xiong W, Li L, Lin L, Shen B, Yang L, Gu S, Zhang Y, Chen Y. Directed Bmp4 expression in neural crest cells generates a genetic model for the rare human bony syngnathia birth defect. Dev Biol. 2014 Jul 15;391(2):170-81. doi
Reddy NA, Gopinath A, Reddy JT, Devanna R, Saravanan P, Rohra MG. MSX ₁ gene variant and non-syndromic clefting
Miller SF, Weinberg SM, Nidey NL, Defay DK, Marazita ML, Wehby GL, Moreno Uribe LM. Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate. J Anat. 2014 Jun;224(6):688-709. doi
Duval N, Daubas P, Bourcier de Carbon C, St Cloment C, Tinevez JY, Lopes M, Ribes V, Robert B. Msx1 and Msx2 act as essential activators of Atoh1 expression in the murine spinal cord. Development. 2014 Apr;141(8):1726-36. doi: 10.1242/dev.099002. PubMed
Wirrig EE, Yutzey KE. Conserved transcriptional regulatory mechanisms in aortic valve development and disease. Arterioscler Thromb Vasc Biol. 2014 Apr;34(4):737-41. doi
Zhu X, Huang S, Zhang L, Wu Y, Chen Y, Tao Y, Wang Y, He S, Shen S, Wu J, Li B, Guo X, He L, Ma G. Constitutive activation of ectodermal β-catenin induces ectopic outgrowths at various positions in mouse embryo and affects abdominal ventral body wall closure. PLoS One. 2014 Mar 19;9(3):e92092. doi: 10.1371/journal.pone.0092092. eCollection 2014. PubMed
Enkhmandakh B, Bayarsaihan D. Genome-wide Chromatin Mapping Defines AP2α in the Etiology of Craniofacial Disorders. Cleft Palate Craniofac J. 2015 Mar;52(2):135-42. doi
Bonds J, Pollan-White S, Xiang L, Mues G, D'Souza R. Is there a link between ovarian cancer and tooth agenesis? Eur J Med Genet. 2014 Apr;57(5):235-9. doi: 10.1016/j.ejmg.2014.02.013. Epub 2014 Mar 12. PubMed
Yoon J, Kim JH, Kim SC, Park JB, Lee JY, Kim J. PV.1 suppresses the expression of FoxD5b during neural induction in Xenopus embryos. Mol Cells. 2014 Mar;37(3):220-5. doi
Ma L, Xu M, Li D, Han Y, Wang Z, Yuan H, Ma J, Zhang W, Jiang H, Pan Y, Wang L. A miRNA-binding-site SNP of MSX1 is Associated with NSOC Susceptibility. J Dent Res. 2014 Jun;93(6):559-64. doi
Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia. Arch Oral Biol. 2014 Mar;59(3):349-53. doi
Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I. Identification of genetic risk factors for maxillary lateral incisor agenesis. J Dent Res. 2014 May;93(5):452-8. doi
Srinivasan S, Hu JS, Currle DS, Fung ES, Hayes WB, Lander AD, Monuki ES. A BMP-FGF morphogen toggle switch drives the ultrasensitive expression of multiple genes in the developing forebrain. PLoS Comput Biol. 2014 Feb 13;10(2):e1003463. doi
Hashmi B, Zarzar LD, Mammoto T, Mammoto A, Jiang A, Aizenberg J, Ingber DE. Developmentally-inspired shrink-wrap polymers for mechanical induction of tissue differentiation. Adv Mater. 2014 May 28;26(20):3253-7. doi: 10.1002/adma.201304995. Epub 2014 Feb 18. PubMed
Reddy NA, Adusumilli G, Devanna R, Mayur RG, Pichai S, Arujnan S. Msx1 Gene Variant - its Association in Isolated Hypodontia
Lee KE, Ko J, Shin TJ, Hyun HK, Lee SH, Kim JW. Oligodontia and curly hair occur with ectodysplasin-a mutations. J Dent Res. 2014 Apr;93(4):371-5. doi: 10.1177/0022034514522059. Epub 2014 Jan 31. PubMed
Chen ZQ, Han XH, Wei QJ, Xing GQ, Cao X. [Comparative analysis of conservation and regulatory network on core transcription factors in mouse inner ear development]. Yi Chuan. 2013 Oct;35(10):1198-208. Chinese. PubMed PMID: 24459893.
Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N. WNT10A mutations account for of population-based isolated oligodontia and show phenotypic correlations. Am J Med Genet A. 2014 Feb;164A(2):353-9. doi
Dai J, Mou Z, Shen S, Dong Y, Yang T, Shen SG. Bioinformatic analysis of Msx1 and Msx2 involved in craniofacial development. J Craniofac Surg. 2014 Jan;25(1):129-34. doi
Kawakami M, Okuda H, Tatsumi K, Kirita T, Wanaka A. Inhibition of Wnt/β-catenin pathway by Dickkopf-1 [corrected] affects midfacial morphogenesis in chick embryo. J Biosci Bioeng. 2014 Jun;117(6):664-9. doi: 10.1016/j.jbiosc.2013.11.015. Epub 2013 Dec 28. Erratum in
Jin JZ, Warner DR, Ding J. Regional divergence of palate medial edge epithelium along the anterior to posterior axis. Int J Dev Biol. 2014;58(9):713-7. doi
Lan Y, Jia S, Jiang R. Molecular patterning of the mammalian dentition. Semin Cell Dev Biol. 2014 Jan-Feb;25-26:61-70. doi
Kimura M, Machida J, Yamaguchi S, Shibata A, Tatematsu T, Miyachi H, Jezewski PA, Nakayama A, Higashi Y, Shimozato K, Tokita Y. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia
Reddy NA, Adusumilli G, Devanna R, Pichai S, Rohra MG, Arjunan S. MSX1 gene variant - its presence in tooth absence - a case control genetic study. J Int Oral Health. 2013 Oct;5(5):20-6. Epub 2013 Oct 26. PubMed
Talln-Walton V, Manzanares-Cspedes MC, Carvalho-Lobato P, Valdivia-Gandur I, Arte S, Nieminen P. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review. Med Oral Patol Oral Cir Bucal. 2014 May 1;19(3):e248-54. Review. PubMed
Haas C, Hanson E, Anjos MJ, Ballantyne KN, Banemann R, Bhoelai B, Borges E, Carvalho M, Courts C, De Cock G, Drobnic K, Dtsch M, Fleming R, Franchi C, Gomes I, Hadzic G, Harbison SA, Harteveld J, Hjort B, Hollard C, Hoff-Olsen P, Hls C, Keyser C, Maroas O, McCallum N, Moore D, Morling N, Niedersttter H, Nol F, Parson W, Phillips C, Popielarz C, Roeder AD, Salvaderi L, Sauer E, Schneider PM, Shanthan G, Court DS, Turansk M, van Oorschot RA, Vennemann M, Vidaki A, Zatkalkov L, Ballantyne J. RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains
Kerosuo L, Bronner ME. Biphasic influence of Miz1 on neural crest development by regulating cell survival and apical adhesion complex formation in the developing neural tube. Mol Biol Cell. 2014 Feb;25(3):347-55. doi: 10.1091/mbc.E13-06-0327. Epub 2013 Dec 4. PubMed
Joksimovic M, Awatramani R. Wnt/β-catenin signaling in midbrain dopaminergic neuron specification and neurogenesis. J Mol Cell Biol. 2014 Feb;6(1):27-33. doi: 10.1093/jmcb/mjt043. Epub 2013 Nov 28. Review. PubMed
Zhao T, Gan Q, Stokes A, Lassiter RN, Wang Y, Chan J, Han JX, Pleasure DE, Epstein JA, Zhou CJ. β-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation. Development. 2014 Jan;141(1):148-57. doi: 10.1242/dev.101550. Epub 2013 Nov 27. PubMed
Xavier D, Arif Y, Murali R, Kishore Kumar S, Vipin Kumar S, Tamang R, Thangaraj K, Bhaskar L. Analysis of microsatellite polymorphisms in South Indian patients with non syndromic cleft lip and palate. Balkan J Med Genet. 2013 Jun;16(1):49-54. doi
Nagel S, Ehrentraut S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA. Oncogenic deregulation of NKL homeobox gene MSX1 in mantle cell lymphoma. Leuk Lymphoma. 2014 Aug;55(8):1893-903. doi
Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families. Genet Mol Res. 2013 Oct 10;12(4):4446-58. doi
Zheng L, Warotayanont R, Stahl J, Kunimatsu R, Klein O, DenBesten PK, Zhang Y. Inductive ability of human developing and differentiated dental mesenchyme. Cells Tissues Organs. 2013;198(2):99-110. doi
Zhou J, Gao Y, Lan Y, Jia S, Jiang R. Pax9 regulates a molecular network involving Bmp4, Fgf10, Shh signaling and the Osr2 transcription factor to control palate morphogenesis. Development. 2013 Dec;140(23):4709-18. doi: 10.1242/dev.099028. Epub 2013 Oct 30. PubMed
Isman E, Nergiz S, Acar H, Sari Z. PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations
Deprez PM, Nichane MG, Lengel BG, Rezshazy R, Nyssen-Behets C. Molecular study of a Hoxa2 gain-of-function in chondrogenesis
Wolff K, Hadadi E, Vas Z. A novel multidisciplinary approach toward a better understanding of cranial suture closure
Mu H, Wu J, Zhu H, Li N, Tang F, Yao X, Yang C, Peng S, Li G, Hua J. The function of Msx1 gene in promoting meiosis of dairy goat male germline stem cells (mGSCs). Cell Biochem Funct. 2013 Dec;31(8):629-35. doi
Chhabra N, Goswami M, Chhabra A. Genetic basis of dental agenesis--molecular genetics patterning clinical dentistry. Med Oral Patol Oral Cir Bucal. 2014 Mar 1;19(2):e112-9. Review. PubMed
Lopez SI, Mundstock KS, Paixo-Crtes VR, Schler-Faccini L, Mundstock CA, Bortolini MC, Salzano FM. MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis. Twin Res Hum Genet. 2013 Dec;16(6):1112-6. doi
Park DS, Seo JH, Hong M, Bang W, Han JK, Choi SC. Role of Sp5 as an essential early regulator of neural crest specification in xenopus. Dev Dyn. 2013 Dec;242(12):1382-94. doi
Ghaderi F, Hekmat S, Ghaderi R, Fardaei M. MSX1 mutation in witkop syndrome; a case report. Iran J Med Sci. 2013 Jun;38(2 Suppl):191-4. PubMed
Feng XY, Zhao YM, Wang WJ, Ge LH. Msx1 regulates proliferation and differentiation of mouse dental mesenchymal cells in culture. Eur J Oral Sci. 2013 Oct;121(5):412-20. doi
Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP. Novel PAX9 mutation associated with syndromic tooth agenesis. Eur J Oral Sci. 2013 Oct;121(5):403-11. doi
Park ES, Woods DC, Tilly JL. Bone morphogenetic protein 4 promotes mammalian oogonial stem cell differentiation via Smad1/5/8 signaling. Fertil Steril. 2013 Nov;100(5):1468-75. doi
Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations. PLoS One. 2013 Aug 22;8(8):e73705. doi
Barembaum M, Bronner ME. Identification and dissection of a key enhancer mediating cranial neural crest specific expression of transcription factor, Ets-1. Dev Biol. 2013 Oct 15;382(2):567-75. doi
Jobbgy-vri G, Pska C, Stiedl P, Trimmel B, Hontvri D, Sos B, Hermann P, Tth Z, Kerekes-Mth B, Nagy D, Sznt I, Nagy , Martonosi M, Nagy K, Hadadi , Szalai C, Hullm G, Temesi G, Antal P, Varga G, Tarjn I. Complex analysis of multiple single nucleotide polymorphisms as putative risk factors of tooth agenesis in the Hungarian population. Acta Odontol Scand. 2014 Apr;72(3):216-27. doi
Song T, Wu D, Wang Y, Li H, Yin N, Zhao Z. SNPs and interaction analyses of IRF6, MSX1 and PAX9 genes in patients with non‑syndromic cleft lip with or without palate. Mol Med Rep. 2013 Oct;8(4):1228-34. doi
Souza LT, Kowalski TW, Collares MV, Flix TM. MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population. Braz J Med Biol Res. 2013 Jul;46(7):555-8. doi
Maury JJ, Chan KK, Zheng L, Bardor M, Choo AB. Excess of O-linked N-acetylglucosamine modifies human pluripotent stem cell differentiation. Stem Cell Res. 2013 Sep;11(2):926-37. doi
Wang J, Xu Y, Chen J, Wang F, Huang R, Wu S, Shu L, Qiu J, Yang Z, Xue J, Wang R, Zhao J, Lai W. PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia
Ruf S, Klimas D, Hnemann M, Jabir S. Genetic background of nonsyndromic oligodontia
Sailer MH, Gerber A, Tostado C, Hutter G, Cordier D, Mariani L, Ritz MF. Non-invasive neural stem cells become invasive in vitro by combined FGF2 and BMP4 signaling. J Cell Sci. 2013 Aug 15;126(Pt 16):3533-40. doi
Dela Pea I, Jeon SJ, Lee E, Ryu JH, Shin CY, Noh M, Cheong JH. Neuronal development genes are key elements mediating the reinforcing effects of methamphetamine, amphetamine, and methylphenidate. Psychopharmacology (Berl). 2013 Dec;230(3):399-413. doi
Ginzelov K, Kripnerov T, Dostlov T. Anomalous findings of number, morphology and size of permanent teeth in 7-10 years children living in the Czech Republic. Prague Med Rep. 2013;114(2):113-22. PubMed
Zhao M, Gupta V, Raj L, Roussel M, Bei M. A network of transcription factors operates during early tooth morphogenesis. Mol Cell Biol. 2013 Aug;33(16):3099-112. doi
Qin H, Xu HZ, Xuan K. Clinical and genetic evaluation of a Chinese family with isolated oligodontia. Arch Oral Biol. 2013 Sep;58(9):1180-6. doi: 10.1016/j.archoralbio.2013.04.007. Epub 2013 May 31. PubMed
Saadi I, Das P, Zhao M, Raj L, Ruspita I, Xia Y, Papaioannou VE, Bei M. Msx1 and Tbx2 antagonistically regulate Bmp4 expression during the bud-to-cap stage transition in tooth development. Development. 2013 Jul;140(13):2697-702. doi: 10.1242/dev.088393. Epub 2013 May 29. PubMed
Seo YJ, Park JW, Kim YH, Baek SH. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients. Angle Orthod. 2013 Nov;83(6):1036-42. doi: 10.2319/020513-104.1. Epub 2013 May 29. PubMed
Prasad VS, Shivani V. Genetic significance of muscle segment homeo box1 gene in South Indian population for cleft lip and palate. Indian J Hum Genet. 2012 Sep;18(3):332-9. doi
Cordell HJ, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, Hall D, van Engelen K, Moorman AF, Zwinderman AH, Barnett P, Koopmann TT, Adriaens ME, Varro A, George AL Jr, dos Remedios C, Bishopric NH, Bezzina CR, O'Sullivan J, Gewillig M, Bu'Lock FA, Winlaw D, Bhattacharya S, Devriendt K, Brook JD, Mulder BJ, Mital S, Postma AV, Lathrop GM, Farrall M, Goodship JA, Keavney BD. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Nat Genet. 2013 Jul;45(7):822-4. doi
Woodcock DJ, Vance KW, Komorowski M, Koentges G, Finkenstdt B, Rand DA. A hierarchical model of transcriptional dynamics allows robust estimation of transcription rates in populations of single cells with variable gene copy number. Bioinformatics. 2013 Jun 15;29(12):1519-25. doi: 10.1093/bioinformatics/btt201. Epub 2013 May 14. PubMed
Reichert JC, Gohlke J, Friis TE, Quent VM, Hutmacher DW. Mesodermal and neural crest derived ovine tibial and mandibular osteoblasts display distinct molecular differences. Gene. 2013 Aug 1;525(1):99-106. doi: 10.1016/j.gene.2013.04.026. Epub 2013 Apr 28. PubMed
Yang Y, Luo L, Xu J, Zhu P, Xue W, Wang J, Li W, Wang M, Cheng K, Liu S, Tang Z, Ring BZ, Su L. Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia. J Dent Res. 2013 Jun;92(6):500-6. doi
Saffarian Tousi N, Velten MF, Bishop TJ, Leong KK, Barkhordar NS, Marshall GW, Loomer PM, Aswath PB, Varanasi VG. Combinatorial effect of Si4+, Ca2+, and Mg2+ released from bioactive glasses on osteoblast osteocalcin expression and biomineralization. Mater Sci Eng C Mater Biol Appl. 2013 Jul 1;33(5):2757-65. doi
Cha J, Sun X, Bartos A, Fenelon J, Lefvre P, Daikoku T, Shaw G, Maxson R, Murphy BD, Renfree MB, Dey SK. A new role for muscle segment homeobox genes in mammalian embryonic diapause. Open Biol. 2013 Apr 24;3(4):130035. doi: 10.1098/rsob.130035. PubMed
Kim NY, Kim YH, Park JW, Baek SH. Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population. J Korean Med Sci. 2013 Apr;28(4):522-6. doi
Vieira AR, D'Souza RN, Mues G, Deeley K, Hsin HY, Kchler EC, Meira R, Patir A, Tannure PN, Lips A, Costa MC, Granjeiro JM, Seymen F, Modesto A. Candidate gene studies in hypodontia suggest role for FGF3. Eur Arch Paediatr Dent. 2013 Dec;14(6):405-10. doi
Zheng LW, Linthicum L, DenBesten PK, Zhang Y. The similarity between human embryonic stem cell-derived epithelial cells and ameloblast-lineage cells. Int J Oral Sci. 2013 Mar;5(1):1-6. doi
Paranaba LM, de Aquino SN, Bufalino A, Martelli-Jnior H, Graner E, Brito LA, e Passos-Bueno MR, Coletta RD, Swerts MS. Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. Med Oral Patol Oral Cir Bucal. 2013 May 1;18(3):e414-20. PubMed
Adams DS, Tseng AS, Levin M. Light-activation of the Archaerhodopsin H(+)-pump reverses age-dependent loss of vertebrate regeneration
Singh N, Gupta M, Trivedi CM, Singh MK, Li L, Epstein JA. Murine craniofacial development requires Hdac3-mediated repression of Msx gene expression. Dev Biol. 2013 May 15;377(2):333-44. doi: 10.1016/j.ydbio.2013.03.008. Epub 2013 Mar 16. PubMed
Chan AA, Hertsenberg AJ, Funderburgh ML, Mann MM, Du Y, Davoli KA, Mich-Basso JD, Yang L, Funderburgh JL. Differentiation of human embryonic stem cells into cells with corneal keratocyte phenotype. PLoS One. 2013;8(2):e56831. doi
Vieux-Rochas M, Bouhali K, Mantero S, Garaffo G, Provero P, Astigiano S, Barbieri O, Caratozzolo MF, Tullo A, Guerrini L, Lallemand Y, Robert B, Levi G, Merlo GR. BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development. PLoS One. 2013;8(1):e51700. doi: 10.1371/journal.pone.0051700. Epub 2013 Jan 29. PubMed
Xie H, Cherrington BD, Meadows JD, Witham EA, Mellon PL. Msx1 homeodomain protein represses the αGSU and GnRH receptor genes during gonadotrope development. Mol Endocrinol. 2013 Mar;27(3):422-36. doi
Alfawaz S, Fong F, Plagnol V, Wong FS, Fearne J, Kelsell DP. Recessive oligodontia linked to a homozygous loss-of-function mutation in the SMOC2 gene. Arch Oral Biol. 2013 May;58(5):462-6. doi
Smith TM, Lozanoff S, Iyyanar PP, Nazarali AJ. Molecular signaling along the anterior-posterior axis of early palate development. Front Physiol. 2013 Jan 7;3:488. doi
Belinsky GS, Sirois CL, Rich MT, Short SM, Moore AR, Gilbert SE, Antic SD. Dopamine receptors in human embryonic stem cell neurodifferentiation. Stem Cells Dev. 2013 May 15;22(10):1522-40. doi
Simes-Costa MS, McKeown SJ, Tan-Cabugao J, Sauka-Spengler T, Bronner ME. Dynamic and differential regulation of stem cell factor FoxD3 in the neural crest is Encrypted in the genome. PLoS Genet. 2012;8(12):e1003142. doi: 10.1371/journal.pgen.1003142. Epub 2012 Dec 20. PubMed
Seo JH, Park DS, Hong M, Chang EJ, Choi SC. Essential role of AWP1 in neural crest specification in Xenopus. Int J Dev Biol. 2013;57(11-12):829-36. doi: 10.1387/ijdb.130109sc. PubMed
Jia S, Zhou J, Gao Y, Baek JA, Martin JF, Lan Y, Jiang R. Roles of Bmp4 during tooth morphogenesis and sequential tooth formation. Development. 2013 Jan 15;140(2):423-32. doi
Cudney SM, Vieira AR. Molecular factors resulting in tooth agenesis and contemporary approaches for regeneration
Rafighdoost H, Hashemi M, Narouei A, Eskanadri-Nasab E, Dashti-Khadivaki G, Taheri M. Association between CDH1 and MSX1 gene polymorphisms and the risk of nonsyndromic cleft lip and/or cleft palate in a southeast Iranian population. Cleft Palate Craniofac J. 2013 Sep;50(5):e98-e104. doi
Wang SK, Chan HC, Makovey I, Simmer JP, Hu JC. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities. PLoS One. 2012;7(12):e51533. doi
Lopes M, Goupille O, Saint Cloment C, Robert B. Msx1 is expressed in retina endothelial cells at artery branching sites. Biol Open. 2012 Apr 15;1(4):376-84. doi
Tangade P, Batra M. Non syndromic oligodontia
Singh KP, Kaushik R, Garg V, Sharma R, George A, Singh MK, Manik RS, Palta P, Singla SK, Chauhan MS. Expression pattern of pluripotent markers in different embryonic developmental stages of buffalo (Bubalus bubalis) embryos and putative embryonic stem cells generated by parthenogenetic activation. Cell Reprogram. 2012 Dec;14(6):530-8. doi
Schiraldi C, Stellavato A, D'Agostino A, Tirino V, d'Aquino R, Woloszyk A, De Rosa A, Laino L, Papaccio G, Mitsiadis TA. Fighting for territories: time-lapse analysis of dental pulp and dental follicle stem cells in co-culture reveals specific migratory capabilities. Eur Cell Mater. 2012 Nov 23;24:426-40. PubMed
Mostowska A, Biedziak B, Zadurska M, Dunin-Wilczynska I, Lianeri M, Jagodzinski PP. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. Clin Genet. 2013 Nov;84(5):429-40. doi
Cardoso ML, Bezerra JF, Oliveira GH, Soares CD, Oliveira SR, de Souza KS, da Silva HP, Silbiger VN, Luchessi AD, Fajardo CM, Hirata RD, Almeida MG, Hirata MH, Rezende AA. MSX1 gene polymorphisms in non-syndromic cleft lip and/or palate. Oral Dis. 2013 Jul;19(5):507-12. doi
Lallemand Y, Moreau J, Cloment CS, Vives FL, Robert B. Generation and characterization of a tamoxifen inducible Msx1(CreERT2) knock-in allele. Genesis. 2013 Feb;51(2):110-9. doi
Medio M, Yeh E, Popelut A, Babajko S, Berdal A, Helms JA. Wnt/β-catenin signaling and Msx1 promote outgrowth of the maxillary prominences. Front Physiol. 2012 Sep 21;3:375. doi
Pal R, Mamidi MK, Das AK, Bhonde R. Comparative analysis of cardiomyocyte differentiation from human embryonic stem cells under 3-D and 2-D culture conditions. J Biosci Bioeng. 2013 Feb;115(2):200-6. doi: 10.1016/j.jbiosc.2012.08.018. Epub 2012 Oct 5. Erratum in
Yardley N, Garca-Castro MI. FGF signaling transforms non-neural ectoderm into neural crest. Dev Biol. 2012 Dec 15;372(2):166-77. doi: 10.1016/j.ydbio.2012.09.006. Epub 2012 Sep 19. PubMed
Allegra A, Marino A, Peregrin PC, Lama A, Garca-Segovia A, Forte GI, Nez-Calonge R, Agueli C, Mazzola S, Volpes A. Endometrial expression of selected genes in patients achieving pregnancy spontaneously or after ICSI and patients failing at least two ICSI cycles. Reprod Biomed Online. 2012 Nov;25(5):481-91. doi
Amano K, Ishiguchi M, Aikawa T, Kimata M, Kishi N, Fujimaki T, Murakami A, Kogo M. Cleft lip in oculodentodigital dysplasia suggests novel roles for connexin43. J Dent Res. 2012 Jul;91(7 Suppl):38S-44S. PubMed
Doan LT, Javier AL, Furr NM, Nguyen KL, Cho KW, Monuki ES. A Bmp reporter with ultrasensitive characteristics reveals that high Bmp signaling is not required for cortical hem fate. PLoS One. 2012;7(9):e44009. doi: 10.1371/journal.pone.0044009. Epub 2012 Sep 11. PubMed
Crton M, van den Boogaard MJ, Maal T, Verhamme L, Fennis W, Carels C, Kuijpers-Jagtman AM, Cune M. Three-dimensional analysis of tooth dimensions in the MSX1-missense mutation. Clin Oral Investig. 2013 Jun;17(5):1437-45. doi: 10.1007/s00784-012-0828-8. Epub 2012 Aug 31. PubMed
Seiz EG, Ramos-Gmez M, Courtois ET, Tnnesen J, Kokaia M, Liste Noya I, Martnez-Serrano A. Human midbrain precursors activate the expected developmental genetic program and differentiate long-term to functional A9 dopamine neurons in vitro. Enhancement by Bcl-X(L). Exp Cell Res. 2012 Nov 15;318(19):2446-59. doi: 10.1016/j.yexcr.2012.07.018. Epub 2012 Aug 2. PubMed
Liang J, Zhu L, Meng L, Chen D, Bian Z. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family. Eur J Oral Sci. 2012 Aug;120(4):278-82. doi
Hurd EA, Micucci JA, Reamer EN, Martin DM. Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice. Mech Dev. 2012 Sep-Dec;129(9-12):308-23. doi
Tang R, Wei F, Wei L, Wang S, Ding G. Osteogenic differentiated periodontal ligament stem cells maintain their immunomodulatory capacity. J Tissue Eng Regen Med. 2014 Mar;8(3):226-32. doi
Metzakopian E, Lin W, Salmon-Divon M, Dvinge H, Andersson E, Ericson J, Perlmann T, Whitsett JA, Bertone P, Ang SL. Genome-wide characterization of Foxa2 targets reveals upregulation of floor plate genes and repression of ventrolateral genes in midbrain dopaminergic progenitors. Development. 2012 Jul;139(14):2625-34. doi
Lai CF, Shao JS, Behrmann A, Krchma K, Cheng SL, Towler DA. TNFR1-activated reactive oxidative species signals up-regulate osteogenic Msx2 programs in aortic myofibroblasts. Endocrinology. 2012 Aug;153(8):3897-910. doi: 10.1210/en.2012-1216. Epub 2012 Jun 8. PubMed
Choi KS, Lee C, Maatouk DM, Harfe BD. Bmp2, Bmp4 and Bmp7 are co-required in the mouse AER for normal digit patterning but not limb outgrowth. PLoS One. 2012;7(5):e37826. doi
Wang J, Abate-Shen C. The MSX1 homeoprotein recruits G9a methyltransferase to repressed target genes in myoblast cells. PLoS One. 2012;7(5):e37647. doi: 10.1371/journal.pone.0037647. Epub 2012 May 22. PubMed
Scerbo P, Girardot F, Vivien C, Markov GV, Luxardi G, Demeneix B, Kodjabachian L, Coen L. Ventx factors function as Nanog-like guardians of developmental potential in Xenopus. PLoS One. 2012;7(5):e36855. doi: 10.1371/journal.pone.0036855. Epub 2012 May 14. PubMed
Boeira Junior BR, Echeverrigaray S. Polymorphism in the MSX1 gene in a family with upper lateral incisor agenesis. Arch Oral Biol. 2012 Oct;57(10):1423-8. doi
Muzaffar M, Selokar NL, Singh KP, Zandi M, Singh MK, Shah RA, Chauhan MS, Singla SK, Palta P, Manik R. Equivalency of buffalo (Bubalus bubalis) embryonic stem cells derived from fertilized, parthenogenetic, and hand-made cloned embryos. Cell Reprogram. 2012 Jun;14(3):267-79. doi
van den Boogaard MJ, Crton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK. Mutations in WNT10A are present in more than half of isolated hypodontia cases. J Med Genet. 2012 May;49(5):327-31. doi
Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, Carles D, Sergi C, Puvabanditsin S, Chen CP, Etchevers HC, Katsanis N, Mercer CL, Calvas P, Jabs EW. OTX2 mutations contribute to the otocephaly-dysgnathia complex. J Med Genet. 2012 Jun;49(6):373-9. doi
Wang J, Abate-Shen C. Transcriptional repression by the Msx1 homeoprotein is associated with global redistribution of the H3K27me3 repressive mark to the nuclear periphery. Nucleus. 2012 Mar 1;3(2):155-61. doi
Kohan-Ghadr HR, Smith LC, Arnold DR, Murphy BD, Lefebvre RC. Aberrant expression of E-cadherin and β-catenin proteins in placenta of bovine embryos derived from somatic cell nuclear transfer. Reprod Fertil Dev. 2012;24(4):588-98. doi
Turan N, Ghalwash MF, Katari S, Coutifaris C, Obradovic Z, Sapienza C. DNA methylation differences at growth related genes correlate with birth weight
Nefzger CM, Su CT, Fabb SA, Hartley BJ, Beh SJ, Zeng WR, Haynes JM, Pouton CW. Lmx1a allows context-specific isolation of progenitors of GABAergic or dopaminergic neurons during neural differentiation of embryonic stem cells. Stem Cells. 2012 Jul;30(7):1349-61. doi
Menezes ME, Mitra A, Shevde LA, Samant RS. DNAJB6 governs a novel regulatory loop determining Wnt/β-catenin signalling activity. Biochem J. 2012 Jun 15;444(3):573-80. doi
Boeira Junior BR, Echeverrigaray S. Dentistry and molecular biology
Leone A, Volponi AA, Renton T, Sharpe PT. In-vitro regulation of odontogenic gene expression in human embryonic tooth cells and SHED cells. Cell Tissue Res. 2012 Jun;348(3):465-73. doi
Koch FP, Weinbach C, Hustert E, Al-Nawas B, Wagner W. GDF-5 and BMP-2 regulate bone cell differentiation by gene expression of MSX1, MSX2, Dlx5, and Runx2 and influence OCN gene expression in vitro. Int J Periodontics Restorative Dent. 2012 Jun;32(3):285-93. PubMed
Aizawa R, Yamada A, Suzuki D, Iimura T, Kassai H, Harada T, Tsukasaki M, Yamamoto G, Tachikawa T, Nakao K, Yamamoto M, Yamaguchi A, Aiba A, Kamijo R. Cdc42 is required for chondrogenesis and interdigital programmed cell death during limb development. Mech Dev. 2012 Mar-Jun;129(1-4):38-50. doi: 10.1016/j.mod.2012.02.002. Epub 2012 Feb 25. PubMed
Nallasamy S, Li Q, Bagchi MK, Bagchi IC. Msx homeobox genes critically regulate embryo implantation by controlling paracrine signaling between uterine stroma and epithelium. PLoS Genet. 2012;8(2):e1002500. doi: 10.1371/journal.pgen.1002500. Epub 2012 Feb 23. PubMed
Mostowska A, Biedziak B, Jagodzinski PP. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars. Arch Oral Biol. 2012 Jun;57(6):790-5. doi
Liang J, Song G, Li Q, Bian Z. Novel missense mutations in PAX9 causing oligodontia. Arch Oral Biol. 2012 Jun;57(6):784-9. doi: 10.1016/j.archoralbio.2011.12.005. Epub 2012 Jan 23. PubMed
Filant J, Zhou H, Spencer TE. Progesterone inhibits uterine gland development in the neonatal mouse uterus. Biol Reprod. 2012 May 10;86(5):146, 1-9. doi
Xiao L, Tsutsui T. Three-dimensional epithelial and mesenchymal cell co-cultures form early tooth epithelium invagination-like structures
Downey MJ, Jeziorska DM, Ott S, Tamai TK, Koentges G, Vance KW, Bretschneider T. Extracting fluorescent reporter time courses of cell lineages from high-throughput microscopy at low temporal resolution. PLoS One. 2011;6(12):e27886. doi
Rauch TA, Wang Z, Wu X, Kernstine KH, Riggs AD, Pfeifer GP. DNA methylation biomarkers for lung cancer. Tumour Biol. 2012 Apr;33(2):287-96. doi: 10.1007/s13277-011-0282-2. Epub 2011 Dec 6. PubMed
Lehoczky JA, Robert B, Tabin CJ. Mouse digit tip regeneration is mediated by fate-restricted progenitor cells. Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20609-14. doi
Austin ED, Menon S, Hemnes AR, Robinson LR, Talati M, Fox KL, Cogan JD, Hamid R, Hedges LK, Robbins I, Lane K, Newman JH, Loyd JE, West J. Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression. Pulm Circ. 2011 Jul-Sep;1(3):389-98. doi
Daikoku T, Cha J, Sun X, Tranguch S, Xie H, Fujita T, Hirota Y, Lydon J, DeMayo F, Maxson R, Dey SK. Conditional deletion of Msx homeobox genes in the uterus inhibits blastocyst implantation by altering uterine receptivity. Dev Cell. 2011 Dec 13;21(6):1014-25. doi
Louryan S, Vanmuylder N, Choa-Duterre M, Jacobs R, Remacle C, Rooze M. [Immunohistochemical study of Dlx1 and Msx1 expression during cephalic development of Dumbo and Wistar rats. Correlation with morphological data]. Morphologie. 2011 Dec;95(311):132-41. doi
Miletich I, Yu WY, Zhang R, Yang K, Caixeta de Andrade S, Pereira SF, Ohazama A, Mock OB, Buchner G, Sealby J, Webster Z, Zhao M, Bei M, Sharpe PT. Developmental stalling and organ-autonomous regulation of morphogenesis. Proc Natl Acad Sci U S A. 2011 Nov 29;108(48):19270-5. doi
Nagel S, Schneider B, Meyer C, Kaufmann M, Drexler HG, Macleod RA. Transcriptional deregulation of homeobox gene ZHX2 in Hodgkin lymphoma. Leuk Res. 2012 May;36(5):646-55. doi
Le Bouffant R, Souquet B, Duval N, Duquenne C, Herv R, Frydman N, Robert B, Habert R, Livera G. Msx1 and Msx2 promote meiosis initiation. Development. 2011 Dec;138(24):5393-402. doi
Zhu J, Yang X, Zhang C, Ge L, Zheng S. A novel nonsense mutation in PAX9 is associated with sporadic hypodontia. Mutagenesis. 2012 May;27(3):313-7. doi: 10.1093/mutage/ger080. Epub 2011 Nov 3. PubMed
Singh VP, Ramu D. Association of MSX1 799 G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients. Int J Paediatr Dent. 2012 May;22(3):228-31. doi
Taniguchi Y, Tanaka O, Sekiguchi M, Takekoshi S, Tsukamoto H, Kimura M, Imai K, Inoko H. Enforced expression of the transcription factor HOXD3 under the control of the Wnt1 regulatory element modulates cell adhesion properties in the developing mouse neural tube. J Anat. 2011 Nov;219(5):589-600. doi: 10.1111/j.1469-7580.2011.01425.x. Epub 2011 Sep 16. PubMed
Mammoto T, Mammoto A, Torisawa YS, Tat T, Gibbs A, Derda R, Mannix R, de Bruijn M, Yung CW, Huh D, Ingber DE. Mechanochemical control of mesenchymal condensation and embryonic tooth organ formation. Dev Cell. 2011 Oct 18;21(4):758-69. doi
Singh K, Dilworth FJ. Redirecting traffic in the nucleus. Dev Cell. 2011 Sep 13;21(3):390-2. doi
Pani SC. The genetic basis of tooth agenesis
Salahshourifar I, Halim AS, Wan Sulaiman WA, Zilfalil BA. Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population. J Hum Genet. 2011 Nov;56(11):755-8. doi
Kouskoura T, Fragou N, Alexiou M, John N, Sommer L, Graf D, Katsaros C, Mitsiadis TA. The genetic basis of craniofacial and dental abnormalities. Schweiz Monatsschr Zahnmed. 2011;121(7-8):636-46. Review. PubMed
Wang J, Kumar RM, Biggs VJ, Lee H, Chen Y, Kagey MH, Young RA, Abate-Shen C. The Msx1 Homeoprotein Recruits Polycomb to the Nuclear Periphery during Development. Dev Cell. 2011 Sep 13;21(3):575-88. doi: 10.1016/j.devcel.2011.07.003. PubMed
Nieto-Miguel T, Calonge M, de la Mata A, Lpez-Paniagua M, Galindo S, de la Paz MF, Corrales RM. A comparison of stem cell-related gene expression in the progenitor-rich limbal epithelium and the differentiating central corneal epithelium. Mol Vis. 2011;17:2102-17. Epub 2011 Aug 10. PubMed
Choi JH, Kim BK, Kim JK, Lee HY, Park JK, Yoon SK. Downregulation of Foxe1 by HR suppresses Msx1 expression in the hair follicles of Hr(Hp) mice. BMB Rep. 2011 Jul;44(7):478-83. doi
Butali A, Mossey PA, Adeyemo WL, Jezewski PA, Onwuamah CK, Ogunlewe MO, Ugboko VI, Adejuyigbe O, Adigun AI, Abdur-Rahman LO, Onah II, Audu RA, Idigbe EO, Mansilla MA, Dragan EA, Petrin AL, Bullard SA, Uduezue AO, Akpata O, Osaguona AO, Olasoji HO, Ligali TO, Kejeh BM, Iseh KR, Olaitan PB, Adebola AR, Efunkoya E, Adesina OA, Oluwatosin OM, Murray JC; NigeriaCRAN Collaboration. Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders. Cleft Palate Craniofac J. 2011 Nov;48(6):646-53. doi: 10.1597/10-133. Epub 2011 Jul 8. PubMed
Song YJ, Lee H. PIAS1 negatively regulates ubiquitination of Msx1 homeoprotein independent of its SUMO ligase activity. Mol Cells. 2011 Sep;32(3):221-6. doi
Lopes M, Goupille O, Saint Cloment C, Lallemand Y, Cumano A, Robert B. Msx genes define a population of mural cell precursors required for head blood vessel maturation. Development. 2011 Jul;138(14):3055-66. doi
Huang YQ, Ma J, Ma M, Deng Y, Li YD, Ren HW, Zhao GZ, Guo SS, Wang YY, Zhang GX, Shi B. Association between MSX1 variants and oral clefts in Han Chinese in western China. DNA Cell Biol. 2011 Dec;30(12):1057-61. doi: 10.1089/dna.2010.1208. Epub 2011 Jun 20. PubMed
Mu X, Xiang G, Rathbone CR, Pan H, Bellayr IH, Walters TJ, Li Y. Slow-adhering stem cells derived from injured skeletal muscle have improved regenerative capacity. Am J Pathol. 2011 Aug;179(2):931-41. doi: 10.1016/j.ajpath.2011.05.004. Epub 2011 Jun 2. PubMed
Bergendal B, Klar J, Stecksn-Blicks C, Norderyd J, Dahl N. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes. Am J Med Genet A. 2011 Jul;155A(7):1616-22. doi
Babajko S, Mary F, Petit S, Fernandes I, Berdal A. Transcriptional regulation of MSX1 natural antisense transcript. Cells Tissues Organs. 2011;194(2-4):151-5. doi
Franz-Odendaal TA. Induction and patterning of intramembranous bone. Front Biosci (Landmark Ed). 2011 Jun 1;16:2734-46. Review. PubMed
Abuqarn M, Allmeling C, Amshoff I, Menger B, Nasser I, Vogt PM, Reimers K. The yeast two hybrid system in a screen for proteins interacting with axolotl (Ambystoma mexicanum) Msx1 during early limb regeneration. Biochim Biophys Acta. 2011 Jul;1814(7):843-9. doi
Kumazaki T, Kurata S, Matsuo T, Mitsui Y, Takahashi T. Establishment of human induced pluripotent stem cell lines from normal fibroblast TIG-1. Hum Cell. 2011 Jun;24(2):96-103. doi
Kong H, Wang Y, Patel M, Mues G, D'Souza RN. Regulation of bmp4 expression in odontogenic mesenchyme
Wang J, Jian F, Chen J, Wang H, Lin Y, Yang Z, Pan X, Lai W. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family. Arch Oral Biol. 2011 Oct;56(10):1027-34. doi
Dunlap KA, Filant J, Hayashi K, Rucker EB 3rd, Song G, Deng JM, Behringer RR, DeMayo FJ, Lydon J, Jeong JW, Spencer TE. Postnatal deletion of Wnt7a inhibits uterine gland morphogenesis and compromises adult fertility in mice. Biol Reprod. 2011 Aug;85(2):386-96. doi
Kantaputra P, Sripathomsawat W. WNT10A and isolated hypodontia. Am J Med Genet A. 2011 May;155A(5):1119-22. doi
Bensoussan-Trigano V, Lallemand Y, Saint Cloment C, Robert B. Msx1 and Msx2 in limb mesenchyme modulate digit number and identity. Dev Dyn. 2011 May;240(5):1190-202. doi
Kamamoto M, Machida J, Yamaguchi S, Kimura M, Ono T, Jezewski PA, Higashi Y, Nakayama A, Shimozato K, Tokita Y. Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia. Eur J Hum Genet. 2011 Aug;19(8):844-50. doi
Gouti M, Briscoe J, Gavalas A. Anterior Hox genes interact with components of the neural crest specification network to induce neural crest fates. Stem Cells. 2011 May;29(5):858-70. doi
Zhou J, Gao Y, Zhang Z, Zhang Y, Maltby KM, Liu Z, Lan Y, Jiang R. Osr2 acts downstream of Pax9 and interacts with both Msx1 and Pax9 to pattern the tooth developmental field. Dev Biol. 2011 May 15;353(2):344-53. doi: 10.1016/j.ydbio.2011.03.012. Epub 2011 Mar 17. PubMed
Chetcuti A, Aktas S, Mackie N, Ulger C, Toruner G, Alkan M, Catchpoole D. Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors. Pediatr Blood Cancer. 2011 Dec 1;57(6):950-7. doi
Wehrhan F, Hyckel P, Amann K, Ries J, Stockmann P, Schlegel K, Neukam F, Nkenke E. Msx-1 is suppressed in bisphosphonate-exposed jaw bone analysis of bone turnover-related cell signalling after bisphosphonate treatment. Oral Dis. 2011 May;17(4):433-42. doi
Wang Y, Kong H, Mues G, D'Souza R. Msx1 mutations
Tapia A, Vilos C, Marn JC, Croxatto HB, Devoto L. Bioinformatic detection of E47, E2F1 and SREBP1 transcription factors as potential regulators of genes associated to acquisition of endometrial receptivity. Reprod Biol Endocrinol. 2011 Jan 27;9:14. doi
Di Renzo F, Rossi F, Prati M, Giavini E, Menegola E. Early genetic control of craniofacial development is affected by the in vitro exposure of rat embryos to the fungicide triadimefon. Birth Defects Res B Dev Reprod Toxicol. 2011 Feb;92(1):77-81. doi
Frenkel B, Blinder D, Penn M. [Isolated oligodontia
Jin YR, Turcotte TJ, Crocker AL, Han XH, Yoon JK. The canonical Wnt signaling activator, R-spondin2, regulates craniofacial patterning and morphogenesis within the branchial arch through ectodermal-mesenchymal interaction. Dev Biol. 2011 Apr 1;352(1):1-13. doi
Sajan SA, Rubenstein JL, Warchol ME, Lovett M. Identification of direct downstream targets of Dlx5 during early inner ear development. Hum Mol Genet. 2011 Apr 1;20(7):1262-73. doi
Matsumura K, Taketomi T, Yoshizaki K, Arai S, Sanui T, Yoshiga D, Yoshimura A, Nakamura S. Sprouty2 controls proliferation of palate mesenchymal cells via fibroblast growth factor signaling. Biochem Biophys Res Commun. 2011 Jan 28;404(4):1076-82. doi
Cheong HS, Lee HC, Park BL, Kim H, Jang MJ, Han YM, Kim SY, Kim YS, Shin HD. Epigenetic modification of retinoic acid-treated human embryonic stem cells. BMB Rep. 2010 Dec;43(12):830-5. doi
Baek JA, Lan Y, Liu H, Maltby KM, Mishina Y, Jiang R. Bmpr1a signaling plays critical roles in palatal shelf growth and palatal bone formation. Dev Biol. 2011 Feb 15;350(2):520-31. doi
Chen JH, Luo YJ, Su YH. The dynamic gene expression patterns of transcription factors constituting the sea urchin aboral ectoderm gene regulatory network. Dev Dyn. 2011 Jan;240(1):250-60. doi
Venza I, Visalli M, Parrillo L, De Felice M, Teti D, Venza M. MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1. Hum Mol Genet. 2011 Mar 1;20(5):1016-25. doi
Paixo-Crtes VR, Braga T, Salzano FM, Mundstock K, Mundstock CA, Bortolini MC. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis. Arch Oral Biol. 2011 Apr;56(4):337-44. doi
Suda N, Ogawa T, Kojima T, Saito C, Moriyama K. Non-syndromic oligodontia with a novel mutation of PAX9. J Dent Res. 2011 Mar;90(3):382-6. doi: 10.1177/0022034510390042. Epub 2010 Nov 22. PubMed
Ayub M, ur-Rehman F, Yasinzai M, Ahmad W. A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia. Int J Dermatol. 2010 Dec;49(12):1399-402. doi
Enright BP, Gu YZ, Snyder RD, Dugyala RR, Obert LA, Treinen KA, McIntyre BS, Veneziale RW. Effects of the histamine H1 antagonist chlorcyclizine on rat fetal palate development. Birth Defects Res B Dev Reprod Toxicol. 2010 Dec;89(6):474-84. doi
Koch FP, Merkel C, Al-Nawas B, Smeets R, Ziebart T, Walter C, Wagner W. Zoledronate, ibandronate and clodronate enhance osteoblast differentiation in a dose dependent manner--a quantitative in vitro gene expression analysis of Dlx5, Runx2, OCN, MSX1 and MSX2. J Craniomaxillofac Surg. 2011 Dec;39(8):562-9. doi: 10.1016/j.jcms.2010.10.007. Epub 2010 Oct 28. PubMed
Wehrhan F, Hyckel P, Ries J, Stockmann P, Nkenke E, Schlegel KA, Neukam FW, Amann K. Expression of Msx-1 is suppressed in bisphosphonate associated osteonecrosis related jaw tissue-etiopathology considerations respecting jaw developmental biology-related unique features. J Transl Med. 2010 Oct 13;8:96. doi
del Río A, Barrio MC, Murillo J, Maldonado E, López-Gordillo Y, Martínez-Sanz E, Martínez ML, Martínez-Álvarez C. Analysis of the presence of cell proliferation-related molecules in the Tgf-β3 null mutant mouse palate reveals misexpression of EGF and Msx-1. Cells Tissues Organs. 2011;193(3):135-50. doi
Dwyer MA, Joseph JD, Wade HE, Eaton ML, Kunder RS, Kazmin D, Chang CY, McDonnell DP. WNT11 expression is induced by estrogen-related receptor alpha and beta-catenin and acts in an autocrine manner to increase cancer cell migration. Cancer Res. 2010 Nov 15;70(22):9298-308. doi
Fuchs A, Inthal A, Herrmann D, Cheng S, Nakatomi M, Peters H, Neubser A. Regulation of Tbx22 during facial and palatal development. Dev Dyn. 2010 Nov;239(11):2860-74. doi
Chung IH, Han J, Iwata J, Chai Y. Msx1 and Dlx5 function synergistically to regulate frontal bone development. Genesis. 2010 Nov;48(11):645-55. doi: 10.1002/dvg.20671. Epub 2010 Nov 2. PubMed
Tirosh-Finkel L, Zeisel A, Brodt-Ivenshitz M, Shamai A, Yao Z, Seger R, Domany E, Tzahor E. BMP-mediated inhibition of FGF signaling promotes cardiomyocyte differentiation of anterior heart field progenitors. Development. 2010 Sep;137(18):2989-3000. doi
Brocher J, Vogel B, Hock R. HMGA1 down-regulation is crucial for chromatin composition and a gene expression profile permitting myogenic differentiation. BMC Cell Biol. 2010 Aug 11;11:64. doi
Nikopensius T, Jagomgi T, Krjutskov K, Tammekivi V, Saag M, Prane I, Piekuse L, Akota I, Barkane B, Krumina A, Ambrozaityte L, Matuleviciene A, Kucinskiene ZA, Lace B, Kucinskas V, Metspalu A. Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. Birth Defects Res A Clin Mol Teratol. 2010 Sep;88(9):748-56. doi
Iyer AK, Miller NL, Yip K, Tran BH, Mellon PL. Enhancers of GnRH transcription embedded in an upstream gene use homeodomain proteins to specify hypothalamic expression. Mol Endocrinol. 2010 Oct;24(10):1949-64. doi: 10.1210/me.2010-0156. Epub 2010 Jul 28. PubMed
Pinho T, Silva-Fernandes A, Bousbaa H, Maciel P. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis. Eur J Orthod. 2010 Oct;32(5):582-8. doi
Meech R, Gomez M, Woolley C, Barro M, Hulin JA, Walcott EC, Delgado J, Makarenkova HP. The homeobox transcription factor Barx2 regulates plasticity of young primary myofibers. PLoS One. 2010 Jul 15;5(7):e11612. doi: 10.1371/journal.pone.0011612. PubMed
Rssler R, Boddeke E, Copray S. Differentiation of non-mesencephalic neural stem cells towards dopaminergic neurons. Neuroscience. 2010 Oct 13;170(2):417-28. doi
Sliwinski T, Synowiec E, Czarny P, Gomulak P, Forma E, Morawiec Z, Morawiec J, Dziki L, Wasylecka M, Blasiak J. The c.469+46_56del mutation in the homeobox MSX1 gene--a novel risk factor in breast cancer? Cancer Epidemiol. 2010 Oct;34(5):652-5. doi
Suazo J, Santos JL, Jara L, Blanco R. Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate. Am J Med Genet A. 2010 Aug;152A(8):2011-6. doi
Bergendal B. Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment. Swed Dent J Suppl. 2010;(205):13-78, 7-8. PubMed
Qi HH, Sarkissian M, Hu GQ, Wang Z, Bhattacharjee A, Gordon DB, Gonzales M, Lan F, Ongusaha PP, Huarte M, Yaghi NK, Lim H, Garcia BA, Brizuela L, Zhao K, Roberts TM, Shi Y. Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development. Nature. 2010 Jul 22;466(7305):503-7. doi: 10.1038/nature09261. Epub 2010 Jul 11. PubMed
Doi T, Puri P, Bannigan J, Thompson J. Msx1 and Msx2 gene expression is downregulated in the cadmium-induced omphalocele in the chick model. J Pediatr Surg. 2010 Jun;45(6):1187-91. doi
Gong Y, Feng HL, He HY, Ge YJ. [Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2010 Jun;32(3):254-9. doi: 10.3881/j.issn.1000-503X.2010.03.003. Chinese. PubMed
Jagomgi T, Nikopensius T, Krjutskov K, Tammekivi V, Viltrop T, Saag M, Metspalu A. MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate. Eur J Oral Sci. 2010 Jun;118(3):213-20. doi: 10.1111/j.1600-0722.2010.00729.x. PubMed
Mostowska A, Hozyasz KK, Wojcicki P, Biedziak B, Paradowska P, Jagodzinski PP. Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population. Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):538-45. doi: 10.1002/bdra.20687. PubMed
Childs AJ, Kinnell HL, Collins CS, Hogg K, Bayne RA, Green SJ, McNeilly AS, Anderson RA. BMP signaling in the human fetal ovary is developmentally regulated and promotes primordial germ cell apoptosis. Stem Cells. 2010 Aug;28(8):1368-78. doi
Jung M, Peterson H, Chavez L, Kahlem P, Lehrach H, Vilo J, Adjaye J. A data integration approach to mapping OCT4 gene regulatory networks operative in embryonic stem cells and embryonal carcinoma cells. PLoS One. 2010 May 21;5(5):e10709. doi
Sun M, Forsman C, Sergi C, Gopalakrishnan R, O'Connor MB, Petryk A. The expression of twisted gastrulation in postnatal mouse brain and functional implications. Neuroscience. 2010 Aug 25;169(2):920-31. doi: 10.1016/j.neuroscience.2010.05.026. Epub 2010 May 20. PubMed
Sato S, Ikeda K, Shioi G, Ochi H, Ogino H, Yajima H, Kawakami K. Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR. Dev Biol. 2010 Aug 1;344(1):158-71. doi: 10.1016/j.ydbio.2010.04.029. Epub 2010 May 21. PubMed
Wang H, Wang L, Pan YC, Ma JQ, Zhang WB. [Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis
Roybal PG, Wu NL, Sun J, Ting MC, Schafer CA, Maxson RE. Inactivation of Msx1 and Msx2 in neural crest reveals an unexpected role in suppressing heterotopic bone formation in the head. Dev Biol. 2010 Jul 1;343(1-2):28-39. doi: 10.1016/j.ydbio.2010.04.007. Epub 2010 Apr 14. PubMed
Maier E, von Hofsten J, Nord H, Fernandes M, Paek H, Hbert JM, Gunhaga L. Opposing Fgf and Bmp activities regulate the specification of olfactory sensory and respiratory epithelial cell fates. Development. 2010 May;137(10):1601-11. doi
Zhou X, Sheng Y, Yang R, Kong X. Nicotine promotes cardiomyocyte apoptosis via oxidative stress and altered apoptosis-related gene expression. Cardiology. 2010;115(4):243-50. doi
Boogerd CJ, Moorman AF, Barnett P. Expression of muscle segment homeobox genes in the developing myocardium. Anat Rec (Hoboken). 2010 Jun;293(6):998-1001. doi
Wang G, Badylak SF, Heber-Katz E, Braunhut SJ, Gudas LJ. The effects of DNA methyltransferase inhibitors and histone deacetylase inhibitors on digit regeneration in mice. Regen Med. 2010 Mar;5(2):201-20. doi
Liu ZR, Shi M, Hu ZL, Zheng MH, Du F, Zhao G, Ding YQ. A refined map of early gene expression in the dorsal rhombomere 1 of mouse embryos. Brain Res Bull. 2010 Apr 29;82(1-2):74-82. doi
Tesfaye D, Regassa A, Rings F, Ghanem N, Phatsara C, Tholen E, Herwig R, Un C, Schellander K, Hoelker M. Suppression of the transcription factor MSX1 gene delays bovine preimplantation embryo development in vitro. Reproduction. 2010 May;139(5):857-70. doi
Talln-Walton V, Nieminen P, Arte S, Ustrell-Torrent JM, Carvalho-Lobato P, Manzanares-Cspedes MC. Oral findings in Midline Syndrome
Kurauchi T, Izutsu Y, Mano M. Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo. Differentiation. 2010 Apr-Jun;79(4-5):251-9. doi
Nakatomi M, Wang XP, Key D, Lund JJ, Turbe-Doan A, Kist R, Aw A, Chen Y, Maas RL, Peters H. Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis. Dev Biol. 2010 Apr 15;340(2):438-49. doi
Ingersoll RG, Hetmanski J, Park JW, Fallin MD, McIntosh I, Wu-Chou YH, Chen PK, Yeow V, Chong SS, Cheah F, Sull JW, Jee SH, Wang H, Wu T, Murray T, Huang S, Ye X, Jabs EW, Redett R, Raymond G, Scott AF, Beaty TH. Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. Eur J Hum Genet. 2010 Jun;18(6):726-32. doi
Wang J, Jian F, Wang S, Wang H, Yang Z, Liao ZY, Lai WL. [Analysis of clinical features and mutation associated with oligodontia]. Hua Xi Kou Qiang Yi Xue Za Zhi. 2009 Dec;27(6):606-9, 613. Chinese. PubMed
el-Shazly M, Bakry R, Tohamy A, Ali WM, Elbakry S, Brown SE, Weatherley-White RC. Attitudes toward children with clefts in rural Muslim and Hindu societies. Ann Plast Surg. 2010 Jun;64(6):780-3. doi: 10.1097/SAP.0b013e3181b0230c. PubMed
Karlsson C, Dehne T, Lindahl A, Brittberg M, Pruss A, Sittinger M, Ringe J. Genome-wide expression profiling reveals new candidate genes associated with osteoarthritis. Osteoarthritis Cartilage. 2010 Apr;18(4):581-92. doi: 10.1016/j.joca.2009.12.002. Epub 2010 Jan 4. PubMed
Houpis CH, Tosios KI, Papavasileiou D, Christopoulos PG, Koutlas IG, Sklavounou A, Alexandridis C. Parathyroid hormone-related peptide (PTHrP), parathyroid hormone/parathyroid hormone-related peptide receptor 1 (PTHR1), and MSX1 protein are expressed in central and peripheral giant cell granulomas of the jaws. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010 Mar;109(3):415-24. doi
El-Sadik AO. Potential sources of stem cells as a regenerative therapy for Parkinson's disease. Stem Cells Cloning. 2010 Dec 6;3:183-91. doi: 10.2147/SCCAA.S14626. Review. PubMed
Chakraborty S, Combs MD, Yutzey KE. Transcriptional regulation of heart valve progenitor cells. Pediatr Cardiol. 2010 Apr;31(3):414-21. doi: 10.1007/s00246-009-9616-x. Epub 2009 Dec 29. Review. PubMed
Napoletano M, Pennino D, Izzo G, de Maria S, Ottaviano R, Ricciardi M, Mancini R, Schiattarella A, Farina E, Metafora S, Carten M, Ritieni A, Minucci S, Morelli F. Ochratoxin A induces craniofacial malformation in mice acting on Dlx5 gene expression. Front Biosci (Elite Ed). 2010 Jan 1;2:133-42. PubMed
Mues G, Kapadia H, Wang Y, D'Souza RN. Genetics and human malformations. J Craniofac Surg. 2009 Sep;20 Suppl 2:1652-4. doi
Song YJ, Lee H. YB1/p32, a nuclear Y-box binding protein 1, is a novel regulator of myoblast differentiation that interacts with Msx1 homeoprotein. Exp Cell Res. 2010 Feb 15;316(4):517-29. doi
Han J, Mayo J, Xu X, Li J, Bringas P Jr, Maas RL, Rubenstein JL, Chai Y. Indirect modulation of Shh signaling by Dlx5 affects the oral-nasal patterning of palate and rescues cleft palate in Msx1-null mice. Development. 2009 Dec;136(24):4225-33. doi
Deng H, Zhu SH, Le WD, Yang HR, Lv HW, Xu HB, Xie WJ, Jankovic J. Examination of the MSX1 gene in patients with Parkinson's disease. Acta Neurol Scand. 2009 Dec;120(6):442-4. doi
Deng M, Pan L, Xie X, Gan L. Requirement for Lmo4 in the vestibular morphogenesis of mouse inner ear. Dev Biol. 2010 Feb 1;338(1):38-49. doi: 10.1016/j.ydbio.2009.11.003. Epub 2009 Nov 10. PubMed
Lee YH, Saint-Jeannet JP. Characterization of molecular markers to assess cardiac cushions formation in Xenopus. Dev Dyn. 2009 Dec;238(12):3257-65. doi: 10.1002/dvdy.22148. PubMed
Romeih M, Cakstina I, Zile MH. Retinoic acid is a negative physiological regulator of N-cadherin during early avian heart morphogenesis. Dev Growth Differ. 2009 Dec;51(9):753-67. doi
Wu SM, Choo AB, Yap MG, Chan KK. Role of Sonic hedgehog signaling and the expression of its components in human embryonic stem cells. Stem Cell Res. 2010 Jan;4(1):38-49. doi
Revet I, Huizenga G, Koster J, Volckmann R, van Sluis P, Versteeg R, Geerts D. MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3. Cancer Lett. 2010 Mar 28;289(2):195-207. doi
Silva ER, Reis-Filho CR, Napimoga MH, Alves JB. Polymorphism in the Msx1 gene associated with hypodontia in a Brazilian family. J Oral Sci. 2009 Sep;51(3):341-5. PubMed
Suzuki D, Yamada A, Amano T, Yasuhara R, Kimura A, Sakahara M, Tsumaki N, Takeda S, Tamura M, Nakamura M, Wada N, Nohno T, Shiroishi T, Aiba A, Kamijo R. Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell death during limb development. Dev Biol. 2009 Nov 15;335(2):396-406. doi: 10.1016/j.ydbio.2009.09.014. Epub 2009 Sep 18. PubMed
Li B, Kuriyama S, Moreno M, Mayor R. The posteriorizing gene Gbx2 is a direct target of Wnt signalling and the earliest factor in neural crest induction. Development. 2009 Oct;136(19):3267-78. doi
Mikkola ML. Controlling the number of tooth rows. Sci Signal. 2009 Aug 25;2(85):pe53. doi
Song L, Li Y, Wang K, Zhou CJ. Cardiac neural crest and outflow tract defects in Lrp6 mutant mice. Dev Dyn. 2010 Jan;239(1):200-10. doi: 10.1002/dvdy.22079. PubMed
Song L, Li Y, Wang K, Wang YZ, Molotkov A, Gao L, Zhao T, Yamagami T, Wang Y, Gan Q, Pleasure DE, Zhou CJ. Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion. Development. 2009 Sep;136(18):3161-71. doi: 10.1242/dev.037440. PubMed
Horst D, Budczies J, Brabletz T, Kirchner T, Hlubek F. Invasion associated up-regulation of nuclear factor kappaB target genes in colorectal cancer. Cancer. 2009 Nov 1;115(21):4946-58. doi
Smith TM, Wang X, Zhang W, Kulyk W, Nazarali AJ. Hoxa2 plays a direct role in murine palate development. Dev Dyn. 2009 Sep;238(9):2364-73. doi: 10.1002/dvdy.22040. PubMed
Gong SG, Mai S, Chung K, Wei K. Flrt2 and Flrt3 have overlapping and non-overlapping expression during craniofacial development. Gene Expr Patterns. 2009 Oct;9(7):497-502. doi
Chen J, Lan Y, Baek JA, Gao Y, Jiang R. Wnt/beta-catenin signaling plays an essential role in activation of odontogenic mesenchyme during early tooth development. Dev Biol. 2009 Oct 1;334(1):174-85. doi: 10.1016/j.ydbio.2009.07.015. Epub 2009 Jul 22. PubMed
Mansouri-Attia N, Aubert J, Reinaud P, Giraud-Delville C, Taghouti G, Galio L, Everts RE, Degrelle S, Richard C, Hue I, Yang X, Tian XC, Lewin HA, Renard JP, Sandra O. Gene expression profiles of bovine caruncular and intercaruncular endometrium at implantation. Physiol Genomics. 2009 Sep 9;39(1):14-27. doi: 10.1152/physiolgenomics.90404.2008. Epub 2009 Jul 21. PubMed
Werner A, Sayer JA. Naturally occurring antisense RNA
Savage J, Conley AJ, Blais A, Skerjanc IS. SOX15 and SOX7 differentially regulate the myogenic program in P19 cells. Stem Cells. 2009 Jun;27(6):1231-43. doi
Dunwell TL, Hesson LB, Pavlova T, Zabarovska V, Kashuba V, Catchpoole D, Chiaramonte R, Brini AT, Griffiths M, Maher ER, Zabarovsky E, Latif F. Epigenetic analysis of childhood acute lymphoblastic leukemia. Epigenetics. 2009 Apr 1;4(3):185-93. Epub 2009 Apr 12. PubMed
Wang Y, Groppe JC, Wu J, Ogawa T, Mues G, D'Souza RN, Kapadia H. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9. Hum Mol Genet. 2009 Aug 1;18(15):2863-74. doi
Wang XP, O'Connell DJ, Lund JJ, Saadi I, Kuraguchi M, Turbe-Doan A, Cavallesco R, Kim H, Park PJ, Harada H, Kucherlapati R, Maas RL. Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood. Development. 2009 Jun;136(11):1939-49. doi: 10.1242/dev.033803. PubMed
Lallemand Y, Bensoussan V, Cloment CS, Robert B. Msx genes are important apoptosis effectors downstream of the Shh/Gli3 pathway in the limb. Dev Biol. 2009 Jul 15;331(2):189-98. doi
MacKenzie B, Wolff R, Lowe N, Billington CJ Jr, Peterson A, Schmidt B, Graf D, Mina M, Gopalakrishnan R, Petryk A. Twisted gastrulation limits apoptosis in the distal region of the mandibular arch in mice. Dev Biol. 2009 Apr 1;328(1):13-23. doi
Zhou F, Leder P, Zuniga A, Dettenhofer M. Formin1 disruption confers oligodactylism and alters Bmp signaling. Hum Mol Genet. 2009 Jul 1;18(13):2472-82. doi
Osrio L, Teillet MA, Catala M. Role of noggin as an upstream signal in the lack of neuronal derivatives found in the avian caudal-most neural crest. Development. 2009 May;136(10):1717-26. doi
Koide Y, Kiyota T, Tonganunt M, Pinkaew D, Liu Z, Kato Y, Hutadilok-Towatana N, Phongdara A, Fujise K. Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation. Biochim Biophys Acta. 2009 May;1790(5):326-38. doi: 10.1016/j.bbagen.2009.01.012. Epub 2009 Feb 7. PubMed
Katoh M, Katoh M. Transcriptional regulation of WNT2B based on the balance of Hedgehog, Notch, BMP and WNT signals. Int J Oncol. 2009 May;34(5):1411-5. PubMed
Pawlowska E, Janik-Papis K, Wisniewska-Jarosinska M, Szczepanska J, Blasiak J. Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth. Tohoku J Exp Med. 2009 Apr;217(4):307-12. PubMed
Wilkie AO. Pitfalls in the phylogenomic evaluation of human disease-causing mutations. J Biol. 2009;8(3):26. doi
Zhuang F, Nguyen MP, Shuler C, Liu YH. Analysis of Msx1 and Msx2 transactivation function in the context of the heat shock 70 (Hspa1b) gene promoter. Biochem Biophys Res Commun. 2009 Apr 3;381(2):241-6. doi: 10.1016/j.bbrc.2009.02.016. Epub 2009 Feb 11. PubMed
Petit S, Meary F, Pibouin L, Jeanny JC, Fernandes I, Poliard A, Hotton D, Berdal A, Babajko S. Autoregulatory loop of Msx1 expression involving its antisense transcripts. J Cell Physiol. 2009 Aug;220(2):303-10. doi: 10.1002/jcp.21762. PubMed
Katerji S, Vanmuylder N, Svoboda M, Rooze M, Louryan S. Expression of Msx1 and Dlx1 during Dumbo rat head development
Barker DM, Beck CW. Overexpression of the transcription factor Msx1 is insufficient to drive complete regeneration of refractory stage Xenopus laevis hindlimbs. Dev Dyn. 2009 Jun;238(6):1366-78. doi
Ishikawa A, Kato T, Susa T, Sano A, Kato Y. Molecular cloning and characterization of porcine homeodomain transcription factor Msx1. J Reprod Dev. 2009 Jun;55(3):278-82. Epub 2009 Mar 4. PubMed
Zhang Z, Lan Y, Chai Y, Jiang R. Antagonistic actions of Msx1 and Osr2 pattern mammalian teeth into a single row. Science. 2009 Feb 27;323(5918):1232-4. doi
Li R, Peng L, Ren L, Tan H, Ye L. Hepatocyte growth factor exerts promoting functions on murine dental papilla cells. J Endod. 2009 Mar;35(3):382-8. doi: 10.1016/j.joen.2008.11.031. PubMed
Benko S, Fantes JA, Amiel J, Kleinjan DJ, Thomas S, Ramsay J, Jamshidi N, Essafi A, Heaney S, Gordon CT, McBride D, Golzio C, Fisher M, Perry P, Abadie V, Ayuso C, Holder-Espinasse M, Kilpatrick N, Lees MM, Picard A, Temple IK, Thomas P, Vazquez MP, Vekemans M, Roest Crollius H, Hastie ND, Munnich A, Etchevers HC, Pelet A, Farlie PG, Fitzpatrick DR, Lyonnet S. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. Nat Genet. 2009 Mar;41(3):359-64. doi
Nieminen P. Genetic basis of tooth agenesis. J Exp Zool B Mol Dev Evol. 2009 Jun 15;312B(4):320-42. doi
Sedano HO, Ocampo-Acosta F, Naranjo-Corona RI, Torres-Arellano ME. Multiple dens invaginatus, mulberry molar and conical teeth. Case report and genetic considerations. Med Oral Patol Oral Cir Bucal. 2009 Feb 1;14(2):E69-72. PubMed
Finnerty JR, Mazza ME, Jezewski PA. Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers. BMC Evol Biol. 2009 Jan 20;9:18. doi
Zhao W, Dai F, Bonafede A, Schafer S, Jung M, Yusuf F, Gamel AJ, Wang J, Brand-Saberi B. Histone deacetylase inhibitor, trichostatin A, affects gene expression patterns during morphogenesis of chicken limb buds in vivo. Cells Tissues Organs. 2009;190(3):121-34. doi
Kemp C, Thiele H, Dankof A, Schmidt G, Lauster C, Fernahl G, Lauster R. Cleft lip and/or palate with monogenic autosomal recessive transmission in Pyrenees shepherd dogs. Cleft Palate Craniofac J. 2009 Jan;46(1):81-8. doi: 10.1597/06-229.1. Epub 2008 Mar 5. PubMed
Govoni KE, Linares GR, Chen ST, Pourteymoor S, Mohan S. T-box 3 negatively regulates osteoblast differentiation by inhibiting expression of osterix and runx2. J Cell Biochem. 2009 Feb 15;106(3):482-90. doi
Illes JC, Winterbottom E, Isaacs HV. Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis. Dev Dyn. 2009 Jan;238(1):194-203. doi
Satterfield MC, Song G, Hayashi K, Bazer FW, Spencer TE. Progesterone regulation of the endometrial WNT system in the ovine uterus. Reprod Fertil Dev. 2008;20(8):935-46. PubMed
Correia AS, Anisimov SV, Roybon L, Li JY, Brundin P. Fibroblast growth factor-20 increases the yield of midbrain dopaminergic neurons derived from human embryonic stem cells. Front Neuroanat. 2007 Dec 30;1:4. doi: 10.3389/neuro.05.004.2007. eCollection 2007. PubMed
Ha Y, Tsukada A, Saito N, Zadworny D, Shimada K. Identification of differentially expressed genes involved in the regression and development of the chicken Mllerian duct. Int J Dev Biol. 2008;52(8):1135-41. doi: 10.1387/ijdb.072441yh. PubMed
van den Boogaard MJ, de Costa D, Krapels IP, Liu F, van Duijn C, Sinke RJ, Lindhout D, Steegers-Theunissen RP. The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts. Hum Genet. 2008 Dec;124(5):525-34. doi
Ruhin-Poncet B, Ghoul-Mazgar S, Hotton D, Capron F, Jaafoura MH, Goubin G, Berdal A. Msx and dlx homeogene expression in epithelial odontogenic tumors. J Histochem Cytochem. 2009 Jan;57(1):69-78. doi
Alonso M, Claros S, Becerra J, Andrades JA. The effect of type I collagen on osteochondrogenic differentiation in adipose-derived stromal cells in vivo. Cytotherapy. 2008;10(6):597-610. doi
Omodei D, Acampora D, Mancuso P, Prakash N, Di Giovannantonio LG, Wurst W, Simeone A. Anterior-posterior graded response to Otx2 controls proliferation and differentiation of dopaminergic progenitors in the ventral mesencephalon. Development. 2008 Oct;135(20):3459-70. doi
Levay AK, Peacock JD, Lu Y, Koch M, Hinton RB Jr, Kadler KE, Lincoln J. Scleraxis is required for cell lineage differentiation and extracellular matrix remodeling during murine heart valve formation in vivo. Circ Res. 2008 Oct 24;103(9):948-56. doi
Callahan N, Modesto A, Meira R, Seymen F, Patir A, Vieira AR. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis. Arch Oral Biol. 2009 Jan;54(1):45-9. doi
Li WL, Cui JJ, Fang QY, Mei LX. [A novel mutation of MSX1 gene in a Chinese pedigree with oligodontia]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2008 Mar;43(3):157-9. Chinese. PubMed
Bonano M, Trbulo C, De Calisto J, Marchant L, Snchez SS, Mayor R, Aybar MJ. A new role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification. Dev Biol. 2008 Nov 1;323(1):114-29. doi: 10.1016/j.ydbio.2008.08.007. Epub 2008 Aug 15. PubMed
De Coster PJ, Marks LA, Martens LC, Huysseune A. Dental agenesis
Berdal A, Molla M, Hotton D, Aoub M, Lzot F, Nfussi JR, Goubin G. Differential impact of MSX1 and MSX2 homeogenes on mouse maxillofacial skeleton. Cells Tissues Organs. 2009;189(1-4):126-32. doi
Postlethwait JH. The zebrafish genome
Babajko S, Petit S, Fernandes I, Mary F, LeBihan J, Pibouin L, Berdal A. Msx1 expression regulation by its own antisense RNA
Lintas C, Persico AM. Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist. J Med Genet. 2009 Jan;46(1):1-8. doi
Zhang L, Tang JL, Liang SZ. [Association of muscle segment homeobox gene 1 polymorphisms with nonsyndromic cleft lip with or without cleft palate]. Hua Xi Kou Qiang Yi Xue Za Zhi. 2008 Jun;26(3):256-7, 261. Chinese. PubMed PMID: 18705505.
Chevrier C, Bahuau M, Perret C, Iovannisci DM, Nelva A, Herman C, Vazquez MP, Francannet C, Robert-Gnansia E, Lammer EJ, Cordier S. Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft. Am J Med Genet A. 2008 Sep 15;146A(18):2396-406. doi
Chen YH, Ishii M, Sucov HM, Maxson RE Jr. Msx1 and Msx2 are required for endothelial-mesenchymal transformation of the atrioventricular cushions and patterning of the atrioventricular myocardium. BMC Dev Biol. 2008 Jul 30;8:75. doi
Han D, Gong Y, Wu H, Zhang X, Yan M, Wang X, Qu H, Feng H, Song S. Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis. Eur J Med Genet. 2008 Nov-Dec;51(6):536-46. doi
Zhu F, Nie RR, Wu L, Liu L, Tang W, Tian WD. [Expression of odontogenic and osteogenic genes in bone marrow mesenchymal stem cells with overexpression of mouse dentin sialophosphoprotein]. Sichuan Da Xue Xue Bao Yi Xue Ban. 2008 Mar;39(2):290-3. Chinese. PubMed
Zhu F, Nie RR, Wu L, Liu L, Tang W, Tian WD. [Spontaneous odontogenic differentiation and critical gene expression of mouse dental papilla mesenchymal cell in vitro]. Sichuan Da Xue Xue Bao Yi Xue Ban. 2008 Mar;39(2):286-9, 297. Chinese. PubMed
Goupille O, Saint Cloment C, Lopes M, Montarras D, Robert B. Msx1 and Msx2 are expressed in sub-populations of vascular smooth muscle cells. Dev Dyn. 2008 Aug;237(8):2187-94. doi
Passman JN, Dong XR, Wu SP, Maguire CT, Hogan KA, Bautch VL, Majesky MW. A sonic hedgehog signaling domain in the arterial adventitia supports resident Sca1+ smooth muscle progenitor cells. Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9349-54. doi
Matalova E, Fleischmannova J, Sharpe PT, Tucker AS. Tooth agenesis
Zhao H, Oka K, Bringas P, Kaartinen V, Chai Y. TGF-beta type I receptor Alk5 regulates tooth initiation and mandible patterning in a type II receptor-independent manner. Dev Biol. 2008 Aug 1;320(1):19-29. doi: 10.1016/j.ydbio.2008.03.045. Epub 2008 Apr 15. PubMed
Wu Z, Nagano I, Takahashi Y. Candidate genes responsible for common and different pathology of infected muscle tissues between Trichinella spiralis and T. pseudospiralis infection. Parasitol Int. 2008 Sep;57(3):368-78. doi: 10.1016/j.parint.2008.03.005. Epub 2008 Apr 9. PubMed
Bailleul-Forestier I, Molla M, Verloes A, Berdal A. The genetic basis of inherited anomalies of the teeth. Part 1
Fujiwara K, Yamada T, Mishima K, Imura H, Sugahara T. Morphological and immunohistochemical studies on cleft palates induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mice. Congenit Anom (Kyoto). 2008 Jun;48(2):68-73. doi
Bensoussan V, Lallemand Y, Moreau J, Cloment CS, Langa F, Robert B. Generation of an Msx2-GFP conditional null allele. Genesis. 2008 May;46(5):276-82. doi
Chang W, Lin Z, Kulessa H, Hebert J, Hogan BL, Wu DK. Bmp4 is essential for the formation of the vestibular apparatus that detects angular head movements. PLoS Genet. 2008 Apr 11;4(4):e1000050. doi
Roybon L, Hjalt T, Christophersen NS, Li JY, Brundin P. Effects on differentiation of embryonic ventral midbrain progenitors by Lmx1a, Msx1, Ngn2, and Pitx3. J Neurosci. 2008 Apr 2;28(14):3644-56. doi: 10.1523/JNEUROSCI.0311-08.2008. PubMed
Mizokami Y, Egashira N, Takekoshi S, Itoh J, Itoh Y, Osamura RY, Matsumae M. Expression of MSX1 in human normal pituitaries and pituitary adenomas. Endocr Pathol. 2008 Spring;19(1):54-61. doi
Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia. Arch Oral Biol. 2008 Aug;53(8):773-9. doi: 10.1016/j.archoralbio.2008.02.012. Epub 2008 Mar 28. PubMed
Miller KA, Davidson S, Liaros A, Barrow J, Lear M, Heine D, Hoppler S, MacKenzie A. Prediction and characterisation of a highly conserved, remote and cAMP responsive enhancer that regulates Msx1 gene expression in cardiac neural crest and outflow tract. Dev Biol. 2008 May 15;317(2):686-94. doi: 10.1016/j.ydbio.2008.02.016. Epub 2008 Feb 21. PubMed
Hu Y, Papagerakis P, Ye L, Feng JQ, Simmer JP, Hu JC. Distal cis-regulatory elements are required for tissue-specific expression of enamelin (Enam). Eur J Oral Sci. 2008 Apr;116(2):113-23. doi
Nie X, Deng CX, Wang Q, Jiao K. Disruption of Smad4 in neural crest cells leads to mid-gestation death with pharyngeal arch, craniofacial and cardiac defects. Dev Biol. 2008 Apr 15;316(2):417-30. doi
Murashima-Suginami A, Takahashi K, Sakata T, Tsukamoto H, Sugai M, Yanagita M, Shimizu A, Sakurai T, Slavkin HC, Bessho K. Enhanced BMP signaling results in supernumerary tooth formation in USAG-1 deficient mouse. Biochem Biophys Res Commun. 2008 May 16;369(4):1012-6. doi
Hu JS, Doan LT, Currle DS, Paff M, Rheem JY, Schreyer R, Robert B, Monuki ES. Border formation in a Bmp gradient reduced to single dissociated cells. Proc Natl Acad Sci U S A. 2008 Mar 4;105(9):3398-403. doi
Boogerd KJ, Wong LY, Christoffels VM, Klarenbeek M, Ruijter JM, Moorman AF, Barnett P. Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43. Cardiovasc Res. 2008 Jun 1;78(3):485-93. doi: 10.1093/cvr/cvn049. Epub 2008 Feb 19. PubMed
Palmieri A, Pezzetti F, Brunelli G, Lo Muzio L, Scarano A, Scapoli L, Martinelli M, Arlotti M, Guerzoni L, Rubini C, Carinci F. Short-period effects of zirconia and titanium on osteoblast microRNAs. Clin Implant Dent Relat Res. 2008 Sep;10(3):200-5. doi
Han M, Yang X, Lee J, Allan CH, Muneoka K. Development and regeneration of the neonatal digit tip in mice. Dev Biol. 2008 Mar 1;315(1):125-35. doi: 10.1016/j.ydbio.2007.12.025. Epub 2007 Dec 27. PubMed
Barthold JS, McCahan SM, Singh AV, Knudsen TB, Si X, Campion L, Akins RE. Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism. J Androl. 2008 May-Jun;29(3):352-66. doi: 10.2164/jandrol.107.003970. Epub 2008 Jan 24. PubMed
Vieira AR. Unraveling human cleft lip and palate research. J Dent Res. 2008 Feb;87(2):119-25. Review. PubMed
Revet I, Huizenga G, Chan A, Koster J, Volckmann R, van Sluis P, ra I, Versteeg R, Geerts D. The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma. Exp Cell Res. 2008 Feb 15;314(4):707-19. doi
Swinnen S, Bailleul-Forestier I, Arte S, Nieminen P, Devriendt K, Carels C. Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia. Orthod Craniofac Res. 2008 Feb;11(1):24-31. doi: 10.1111/j.1601-6343.2008.00410.x. PubMed
Freed WJ, Chen J, Bckman CM, Schwartz CM, Vazin T, Cai J, Spivak CE, Lupica CR, Rao MS, Zeng X. Gene expression profile of neuronal progenitor cells derived from hESCs
Otero L, Gutirrez S, Chves M, Vargas C, Brmudez L. Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population. Cleft Palate Craniofac J. 2007 Nov;44(6):653-6. doi
Wu PA, Li YL, Wu HJ, Wang K, Fan GZ. [Transmission disequilibrium test for nonsyndromic cleft lip and palate and segment homeobox gene-1 gene]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2007 Sep;42(9):561-3. Chinese. PubMed
Kim J, Lauderdale JD. Overexpression of pairedless Pax6 in the retina disrupts corneal development and affects lens cell survival. Dev Biol. 2008 Jan 1;313(1):434-54. Epub 2007 Nov 9. PubMed
Wescott DC, Pinkerton MN, Gaffey BJ, Beggs KT, Milne TJ, Meikle MC. Osteogenic gene expression by human periodontal ligament cells under cyclic tension. J Dent Res. 2007 Dec;86(12):1212-6. PubMed
Talln-Walton V, Manzanares-Cspedes MC, Arte S, Carvalho-Lobato P, Valdivia-Gandur I, Garcia-Susperregui A, Ventura F, Nieminen P. Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies. Eur J Oral Sci. 2007 Dec;115(6):427-32. PubMed
Liu F, Chu EY, Watt B, Zhang Y, Gallant NM, Andl T, Yang SH, Lu MM, Piccolo S, Schmidt-Ullrich R, Taketo MM, Morrisey EE, Atit R, Dlugosz AA, Millar SE. Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis. Dev Biol. 2008 Jan 1;313(1):210-24. Epub 2007 Oct 23. PubMed
Kapadia H, Mues G, D'Souza R. Genes affecting tooth morphogenesis. Orthod Craniofac Res. 2007 Nov;10(4):237-44. Review. PubMed
Kumar SD, Dheen ST, Tay SS. Maternal diabetes induces congenital heart defects in mice by altering the expression of genes involved in cardiovascular development. Cardiovasc Diabetol. 2007 Oct 30;6:34. PubMed
Wu L, Zhu F, Wu Y, Lin Y, Nie X, Jing W, Qiao J, Liu L, Tang W, Zheng X, Tian W. Dentin sialophosphoprotein-promoted mineralization and expression of odontogenic genes in adipose-derived stromal cells. Cells Tissues Organs. 2008;187(2):103-12. Epub 2007 Oct 23. PubMed
Jia Q, McDill BW, Li SZ, Deng C, Chang CP, Chen F. Smad signaling in the neural crest regulates cardiac outflow tract remodeling through cell autonomous and non-cell autonomous effects. Dev Biol. 2007 Nov 1;311(1):172-84. Epub 2007 Aug 31. PubMed
Zhao J, Hu Q, Chen Y, Luo S, Bao L, Xu Y. A novel missense mutation in the paired domain of human PAX9 causes oligodontia. Am J Med Genet A. 2007 Nov 1;143A(21):2592-7. PubMed
Li YM, Yang L, Ding Y, Li D. [Effect of cyclic-tension force on the expression of osteogenesis genes in human periodontal ligament cells]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2007 Jun;42(6):368-72. Chinese. PubMed
Liao X, Lee GS, Shimizu H, Collins MD. Comparative molecular pathology of cadmium- and all-trans-retinoic acid-induced postaxial forelimb ectrodactyly. Toxicol Appl Pharmacol. 2007 Nov 15;225(1):47-60. Epub 2007 Jun 21. PubMed
Aoub M, Lzot F, Molla M, Castaneda B, Robert B, Goubin G, Nfussi JR, Berdal A. Msx2 -/- transgenic mice develop compound amelogenesis imperfecta, dentinogenesis imperfecta and periodental osteopetrosis. Bone. 2007 Nov;41(5):851-9. Epub 2007 Aug 15. PubMed
Miller KA, Barrow J, Collinson JM, Davidson S, Lear M, Hill RE, Mackenzie A. A highly conserved Wnt-dependent TCF4 binding site within the proximal enhancer of the anti-myogenic Msx1 gene supports expression within Pax3-expressing limb bud muscle precursor cells. Dev Biol. 2007 Nov 15;311(2):665-78. Epub 2007 Jul 26. PubMed
Cobourne MT. Familial human hypodontia--is it all in the genes? Br Dent J. 2007 Aug 25;203(4):203-8. Review. PubMed
Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth. Eur J Oral Sci. 2007 Aug;115(4):330-3. PubMed
Welsh IC, Hagge-Greenberg A, O'Brien TP. A dosage-dependent role for Spry2 in growth and patterning during palate development. Mech Dev. 2007 Sep-Oct;124(9-10):746-61. Epub 2007 Jul 10. PubMed
Han J, Ishii M, Bringas P Jr, Maas RL, Maxson RE Jr, Chai Y. Concerted action of Msx1 and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development. Mech Dev. 2007 Sep-Oct;124(9-10):729-45. Epub 2007 Jul 10. PubMed
Ghanem N, Hlker M, Rings F, Jennen D, Tholen E, Sirard MA, Torner H, Kanitz W, Schellander K, Tesfaye D. Alterations in transcript abundance of bovine oocytes recovered at growth and dominance phases of the first follicular wave. BMC Dev Biol. 2007 Jul 27;7:90. PubMed
Fu H, Ishii M, Gu Y, Maxson R. Conditional alleles of Msx1 and Msx2. Genesis. 2007 Aug;45(8):477-81. PubMed
Kapadia H, Mues G, D'Souza R. Genes affecting tooth morphogenesis. Orthod Craniofac Res. 2007 Aug;10(3):105-13. Review. Erratum in
Prakash N, Wurst W. A Wnt signal regulates stem cell fate and differentiation in vivo. Neurodegener Dis. 2007;4(4):333-8. Review. PubMed
Carinci F, Scapoli L, Palmieri A, Zollino I, Pezzetti F. Human genetic factors in nonsyndromic cleft lip and palate
Chen YH, Ishii M, Sun J, Sucov HM, Maxson RE Jr. Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract. Dev Biol. 2007 Aug 15;308(2):421-37. Epub 2007 Jun 4. PubMed
Liu H, Xu S, Wang Y, Mazerolle C, Thurig S, Coles BL, Ren JC, Taketo MM, van der Kooy D, Wallace VA. Ciliary margin transdifferentiation from neural retina is controlled by canonical Wnt signaling. Dev Biol. 2007 Aug 1;308(1):54-67. Epub 2007 May 16. PubMed
Vi-Fane B, Fernandes I, Davideau JL. [Msx1 and its influence on craniofacial growth]. Orthod Fr. 2007 Mar;78(1):39-48. Review. French. PubMed
Seifi M, Kazemi B, Golkar P. The role of MSX1 in tooth agenesis in Iranians. Int J Paediatr Dent. 2007 Jul;17(4):254-8. PubMed
Wu PA, Li YL, Fan GZ, Wang K. [Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):325-7. Chinese. PubMed
Hu JC, Simmer JP. Developmental biology and genetics of dental malformations. Orthod Craniofac Res. 2007 May;10(2):45-52. Review. PubMed PMID: 17552940.
Sirchia R, Luparello C. Mid-region parathyroid hormone-related protein (PTHrP) and gene expression of MDA-MB231 breast cancer cells. Biol Chem. 2007 May;388(5):457-65. PubMed
Endo T. Stem cells and plasticity of skeletal muscle cell differentiation: potential application to cell therapy for degenerative muscular diseases. Regen Med. 2007 May;2(3):243-56. Review. PubMed
Binato R, Pizzatti L, Abdelhay E. Otx2 is a putative candidate to activate mice Msx1 gene from distal enhancer. Biochem Biophys Res Commun. 2007 Jun 29;358(2):655-60. Epub 2007 May 7. PubMed
Lin D, Huang Y, He F, Gu S, Zhang G, Chen Y, Zhang Y. Expression survey of genes critical for tooth development in the human embryonic tooth germ. Dev Dyn. 2007 May;236(5):1307-12. PubMed
Park J, Park BY, Kim HS, Lee JE, Suh I, Nam CM, Kang DR, Kim S, Yun JE, Go EN, Jee SH, Beaty TH. MSX1 polymorphism associated with risk of oral cleft in Korea
Vieira AR, Modesto A, Meira R, Barbosa AR, Lidral AC, Murray JC. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. Am J Med Genet A. 2007 Mar 15;143A(6):538-45. PubMed
Handrigan GR, Wassersug RJ. The anuran Bauplan
Feng HL, Zhang XX, Wu H. [Research advances in tooth agenesis]. Beijing Da Xue Xue Bao Yi Xue Ban. 2007 Feb 18;39(1):13-7. Chinese. PubMed
Li Q, Ding J. Gene expression analysis reveals that formation of the mouse anterior secondary palate involves recruitment of cells from the posterior side. Int J Dev Biol. 2007;51(2):167-72. PubMed
Pardo V RA, Castillo T S, Vieira AR. [Genetic studies of a Chilean family with three different dental anomalies]. Rev Med Chil. 2006 Dec;134(12):1541-8. Epub 2007 Jan 24. Spanish. PubMed
Yamanishi T, Katsu K, Funahashi J, Yumoto E, Yokouchi Y. Dan is required for normal morphogenesis and patterning in the developing chick inner ear. Dev Growth Differ. 2007 Jan;49(1):13-26. PubMed
Oka K, Oka S, Sasaki T, Ito Y, Bringas P Jr, Nonaka K, Chai Y. The role of TGF-beta signaling in regulating chondrogenesis and osteogenesis during mandibular development. Dev Biol. 2007 Mar 1;303(1):391-404. Epub 2006 Nov 21. PubMed
Shames DS, Girard L, Gao B, Sato M, Lewis CM, Shivapurkar N, Jiang A, Perou CM, Kim YH, Pollack JR, Fong KM, Lam CL, Wong M, Shyr Y, Nanda R, Olopade OI, Gerald W, Euhus DM, Shay JW, Gazdar AF, Minna JD. A genome-wide screen for promoter methylation in lung cancer identifies novel methylation markers for multiple malignancies. PLoS Med. 2006 Dec;3(12):e486. PubMed
Slayton R. DNA sequence variations in the genes MSX1 and TGFA may lead to developmentally missing teeth. J Evid Based Dent Pract. 2005 Sep;5(3):160-1. PubMed
Cohen MM Jr. The new bone biology
Nie X. Developmentally regulated expression of MSX1, MSX2 and Fgfs in the developing mouse cranial base. Angle Orthod. 2006 Nov;76(6):990-5. PubMed PMID: 17090159.
Tolarov MM, Poulton D, Aubert MM, Oh H, Ellerhorst T, Mosby T, Tolar M, Boyd RL. Pacific Craniofacial Team and Cleft Prevention Program. J Calif Dent Assoc. 2006 Oct;34(10):823-30. PubMed
Sargent TD. Transcriptional regulation at the neural plate border. Adv Exp Med Biol. 2006;589:32-44. Review. PubMed
Hayashi K, Nakamura S, Nishida W, Sobue K. Bone morphogenetic protein-induced MSX1 and MSX2 inhibit myocardin-dependent smooth muscle gene transcription. Mol Cell Biol. 2006 Dec;26(24):9456-70. Epub 2006 Oct 9. PubMed
Burbach JP, Smidt MP. Molecular programming of stem cells into mesodiencephalic dopaminergic neurons. Trends Neurosci. 2006 Nov;29(11):601-3. Epub 2006 Oct 9. Review. PubMed
Lind GE, Skotheim RI, Fraga MF, Abeler VM, Esteller M, Lothe RA. Novel epigenetically deregulated genes in testicular cancer include homeobox genes and SCGB3A1 (HIN-1). J Pathol. 2006 Dec;210(4):441-9. PubMed
Gan Q, Yoshida T, McDonald OG, Owens GK. Concise review
El-Sayed A, Hoelker M, Rings F, Salilew D, Jennen D, Tholen E, Sirard MA, Schellander K, Tesfaye D. Large-scale transcriptional analysis of bovine embryo biopsies in relation to pregnancy success after transfer to recipients. Physiol Genomics. 2006 Dec 13;28(1):84-96. Epub 2006 Oct 3. PubMed
Britanova O, Depew MJ, Schwark M, Thomas BL, Miletich I, Sharpe P, Tarabykin V. Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development. Am J Hum Genet. 2006 Oct;79(4):668-78. Epub 2006 Aug 30. PubMed
Allan CH, Fleckman P, Fernandes RJ, Hager B, James J, Wisecarver Z, Satterstrom FK, Gutierrez A, Norman A, Pirrone A, Underwood RA, Rubin BP, Zhang M, Ramay HR, Clark JM. Tissue response and Msx1 expression after human fetal digit tip amputation in vitro. Wound Repair Regen. 2006 Jul-Aug;14(4):398-404. PubMed
Beck CW, Christen B, Barker D, Slack JM. Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles. Mech Dev. 2006 Sep;123(9):674-88. Epub 2006 Jul 6. PubMed
Chishti MS, Muhammad D, Haider M, Ahmad W. A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families. J Hum Genet. 2006;51(10):872-878. doi: 10.1007/s10038-006-0037-x. Epub 2006 Aug 24. PubMed
Lazzari G, Colleoni S, Giannelli SG, Brunetti D, Colombo E, Lagutina I, Galli C, Broccoli V. Direct derivation of neural rosettes from cloned bovine blastocysts
Gerits A, Nieminen P, De Muynck S, Carels C. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype. Orthod Craniofac Res. 2006 Aug;9(3):129-36. PubMed
Tongkobpetch S, Siriwan P, Shotelersuk V. MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population. J Hum Genet. 2006;51(8):671. doi: 10.1007/s10038-006-0006-4. Epub 2006 Jul 26. PubMed
Prakash N, Wurst W. Genetic networks controlling the development of midbrain dopaminergic neurons. J Physiol. 2006 Sep 1;575(Pt 2):403-10. Epub 2006 Jul 6. Review. PubMed
Baffi MO, Moran MA, Serra R. Tgfbr2 regulates the maintenance of boundaries in the axial skeleton. Dev Biol. 2006 Aug 15;296(2):363-74. Epub 2006 Jun 7. PubMed
Komori T. Regulation of osteoblast differentiation by transcription factors. J Cell Biochem. 2006 Dec 1;99(5):1233-9. Review. PubMed
Angello JC, Kaestner S, Welikson RE, Buskin JN, Hauschka SD. BMP induction of cardiogenesis in P19 cells requires prior cell-cell interaction(s). Dev Dyn. 2006 Aug;235(8):2122-33. PubMed
Modesto A, Moreno LM, Krahn K, King S, Lidral AC. MSX1 and orofacial clefting with and without tooth agenesis. J Dent Res. 2006 Jun;85(6):542-6. PubMed
Sarapura VD, Wood WM, Woodmansee WW, Haakinson DJ, Dowding JM, Gordon DF, Ridgway EC. Pituitary tumors arising from glycoprotein hormone alpha-subunit-deficient mice contain transcription factors and receptors present in thyrotropes. Pituitary. 2006;9(1):11-8. PubMed
Lace B, Vasiljeva I, Dundure I, Barkane B, Akota I, Krumina A. Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate. Stomatologija. 2006;8(1):21-4. PubMed
Mostowska A, Biedziak B, Trzeciak WH. A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1
Gupta V, Bei M. Modification of Msx1 by SUMO-1. Biochem Biophys Res Commun. 2006 Jun 23;345(1):74-7. Epub 2006 Apr 19. PubMed
Gjessing HK, Lie RT. Case-parent triads
Ogawa T, Kapadia H, Feng JQ, Raghow R, Peters H, D'Souza RN. Functional consequences of interactions between Pax9 and Msx1 genes in normal and abnormal tooth development. J Biol Chem. 2006 Jul 7;281(27):18363-9. Epub 2006 May 1. PubMed
Ovchinnikov DA, Selever J, Wang Y, Chen YT, Mishina Y, Martin JF, Behringer RR. BMP receptor type IA in limb bud mesenchyme regulates distal outgrowth and patterning. Dev Biol. 2006 Jul 1;295(1):103-15. Epub 2006 Apr 21. PubMed PMID: 16630606.
Song Y, Zhang Z, Yu X, Yan M, Zhang X, Gu S, Stuart T, Liu C, Reiser J, Zhang Y, Chen Y. Application of lentivirus-mediated RNAi in studying gene function in mammalian tooth development. Dev Dyn. 2006 May;235(5):1334-44. PubMed
Storm EE, Garel S, Borello U, Hebert JM, Martinez S, McConnell SK, Martin GR, Rubenstein JL. Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers. Development. 2006 May;133(9):1831-44. PubMed
Lee H, Quinn JC, Prasanth KV, Swiss VA, Economides KD, Camacho MM, Spector DL, Abate-Shen C. PIAS1 confers DNA-binding specificity on the Msx1 homeoprotein. Genes Dev. 2006 Apr 1;20(7):784-94. PubMed
Sharrocks AD. PIAS proteins and transcriptional regulation--more than just SUMO E3 ligases? Genes Dev. 2006 Apr 1;20(7):754-8. Review. PubMed PMID: 16600908.
Khadka D, Luo T, Sargent TD. Msx1 and Msx2 have shared essential functions in neural crest but may be dispensable in epidermis and axis formation in Xenopus. Int J Dev Biol. 2006;50(5):499-502. PubMed
Uehara N, Unami A, Kiyozuka Y, Shikata N, Oishi Y, Tsubura A. Parous mammary glands exhibit distinct alterations in gene expression and proliferation responsiveness to carcinogenic stimuli in Lewis rats. Oncol Rep. 2006 Apr;15(4):903-11. PubMed
Kim JW, Simmer JP, Lin BP, Hu JC. Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res. 2006 Mar;85(3):267-71. PubMed PMID: 16498076; PubMed Central PMCID
Hill TP, Taketo MM, Birchmeier W, Hartmann C. Multiple roles of mesenchymal beta-catenin during murine limb patterning. Development. 2006 Apr;133(7):1219-29. Epub 2006 Feb 22. PubMed
Kapadia H, Frazier-Bowers S, Ogawa T, D'Souza RN. Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis. Eur J Hum Genet. 2006 Apr;14(4):403-9. PubMed
Mitsiadis TA, Caton J, Cobourne M. Waking-up the sleeping beauty
Pujades C, Kamaid A, Alsina B, Giraldez F. BMP-signaling regulates the generation of hair-cells. Dev Biol. 2006 Apr 1;292(1):55-67. Epub 2006 Feb 3. PubMed
Johnston JD, Klosen P, Barrett P, Hazlerigg DG. Regulation of MT melatonin receptor expression in the foetal rat pituitary. J Neuroendocrinol. 2006 Jan;18(1):50-6. PubMed
Verdyck P, Blaumeiser B, Holder-Espinasse M, Van Hul W, Wuyts W. Adams-Oliver syndrome
Andersson E, Tryggvason U, Deng Q, Friling S, Alekseenko Z, Robert B, Perlmann T, Ericson J. Identification of intrinsic determinants of midbrain dopamine neurons. Cell. 2006 Jan 27;124(2):393-405. PubMed
Mostowska A, Biedziak B, Jagodzinski PP. Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis. J Hum Genet. 2006;51(3):262-266. doi
Kriangkrai R, Iseki S, Eto K, Chareonvit S. Dual odontogenic origins develop at the early stage of rat maxillary incisor development. Anat Embryol (Berl). 2006 Mar;211(2):101-8. Epub 2006 Jan 17. PubMed
Tereshina MB, Zaraisky AG, Novoselov VV. Ras-dva, a member of novel family of small GTPases, is required for the anterior ectoderm patterning in the Xenopus laevis embryo. Development. 2006 Feb;133(3):485-94. PubMed
Yamashita S, Tsujino Y, Moriguchi K, Tatematsu M, Ushijima T. Chemical genomic screening for methylation-silenced genes in gastric cancer cell lines using 5-aza-2'-deoxycytidine treatment and oligonucleotide microarray. Cancer Sci. 2006 Jan;97(1):64-71. PubMed
Levi G, Mantero S, Barbieri O, Cantatore D, Paleari L, Beverdam A, Genova F, Robert B, Merlo GR. Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formation. Mech Dev. 2006 Jan;123(1):3-16. Epub 2005 Dec 5. PubMed PMID: 16330189.
Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Flix TM, Rahimov F, Harrington J, Schultz RR, Watanabe Y, Johnson M, Fang J, O'Brien SE, Orioli IM, Castilla EE, Fitzpatrick DR, Jiang R, Marazita ML, Murray JC. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS Genet. 2005 Dec;1(6):e64. Epub 2005 Dec 2. PubMed
Perry GH, Verrelli BC, Stone AC. Molecular evolution of the primate developmental genes MSX1 and PAX9. Mol Biol Evol. 2006 Mar;23(3):644-54. Epub 2005 Dec 2. PubMed
Ma L, Lu MF, Schwartz RJ, Martin JF. Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning. Development. 2005 Dec;132(24):5601-11. PubMed
Hilliard SA, Yu L, Gu S, Zhang Z, Chen YP. Regional regulation of palatal growth and patterning along the anterior-posterior axis in mice. J Anat. 2005 Nov;207(5):655-67. Review. PubMed
Depew MJ, Simpson CA, Morasso M, Rubenstein JL. Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development. J Anat. 2005 Nov;207(5):501-61. Review. PubMed
Han M, Yang X, Taylor G, Burdsal CA, Anderson RA, Muneoka K. Limb regeneration in higher vertebrates
Lidral AC, Moreno LM. Progress toward discerning the genetics of cleft lip. Curr Opin Pediatr. 2005 Dec;17(6):731-9. Review. PubMed
Galle S, Yanze N, Seipel K. The homeobox gene Msx in development and transdifferentiation of jellyfish striated muscle. Int J Dev Biol. 2005;49(8):961-7. PubMed
Chen J, Leong SY, Schachner M. Differential expression of cell fate determinants in neurons and glial cells of adult mouse spinal cord after compression injury. Eur J Neurosci. 2005 Oct;22(8):1895-906. PubMed PMID: 16262629.
Karafiat V, Dvorakova M, Krejci E, Kralova J, Pajer P, Snajdr P, Mandikova S, Bartunek P, Grim M, Dvorak M. Transcription factor c-Myb is involved in the regulation of the epithelial-mesenchymal transition in the avian neural crest. Cell Mol Life Sci. 2005 Nov;62(21):2516-25. PubMed
Ishii M, Han J, Yen HY, Sucov HM, Chai Y, Maxson RE Jr. Combined deficiencies of Msx1 and Msx2 cause impaired patterning and survival of the cranial neural crest. Development. 2005 Nov;132(22):4937-50. Epub 2005 Oct 12. PubMed
Santagati F, Minoux M, Ren SY, Rijli FM. Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis. Development. 2005 Nov;132(22):4927-36. Epub 2005 Oct 12. PubMed
Johnson EB, Hammer RE, Herz J. Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice. Hum Mol Genet. 2005 Nov 15;14(22):3523-38. Epub 2005 Oct 5. PubMed
Nino-Rosales ML, Patel PI. Genes underlying familial hypodontia
Ramos C, Robert B. msh/Msx gene family in neural development. Trends Genet. 2005 Nov;21(11):624-32. Epub 2005 Sep 19. Review. PubMed
Coudert AE, Pibouin L, Vi-Fane B, Thomas BL, Macdougall M, Choudhury A, Robert B, Sharpe PT, Berdal A, Lezot F. Expression and regulation of the Msx1 natural antisense transcript during development. Nucleic Acids Res. 2005 Sep 12;33(16):5208-18. Print 2005. PubMed
Suzuki M, Satoh A, Ide H, Tamura K. Nerve-dependent and -independent events in blastema formation during Xenopus froglet limb regeneration. Dev Biol. 2005 Oct 1;286(1):361-75. PubMed
Wang J, Sridurongrit S, Dudas M, Thomas P, Nagy A, Schneider MD, Epstein JA, Kaartinen V. Atrioventricular cushion transformation is mediated by ALK2 in the developing mouse heart. Dev Biol. 2005 Oct 1;286(1):299-310. PubMed PMID: 16140292; PubMed Central PMCID
Taneyhill LA, Bronner-Fraser M. Dynamic alterations in gene expression after Wnt-mediated induction of avian neural crest. Mol Biol Cell. 2005 Nov;16(11):5283-93. Epub 2005 Aug 31. PubMed
Binato R, Alvarez Martinez CE, Pizzatti L, Robert B, Abdelhay E. SMAD 8 binding to mice Msx1 basal promoter is required for transcriptional activation. Biochem J. 2006 Jan 1;393(Pt 1):141-50. PubMed
Camilleri S. Maxillary canine anomalies and tooth agenesis. Eur J Orthod. 2005 Oct;27(5):450-6. Epub 2005 Aug 10. PubMed
Rice R, Thesleff I, Rice DP. Regulation of Twist, Snail, and Id1 is conserved between the developing murine palate and tooth. Dev Dyn. 2005 Sep;234(1):28-35. PubMed
Gersch RP, Lombardo F, McGovern SC, Hadjiargyrou M. Reactivation of Hox gene expression during bone regeneration. J Orthop Res. 2005 Jul;23(4):882-90. Epub 2005 Mar 23. PubMed
Rave-Harel N, Miller NL, Givens ML, Mellon PL. The Groucho-related gene family regulates the gonadotropin-releasing hormone gene through interaction with the homeodomain proteins MSX1 and OCT1. J Biol Chem. 2005 Sep 2;280(35):30975-83. Epub 2005 Jul 7. PubMed
Ohazama A. [The possibility of tooth regenerative therapy]. Clin Calcium. 2005 Jul;15(7):81-5. Review. Japanese. PubMed
Schnapp E, Kragl M, Rubin L, Tanaka EM. Hedgehog signaling controls dorsoventral patterning, blastema cell proliferation and cartilage induction during axolotl tail regeneration. Development. 2005 Jul;132(14):3243-53. PubMed
Etheredge AJ, Christensen K, Del Junco D, Murray JC, Mitchell LE. Evaluation of two methods for assessing gene-environment interactions using data from the Danish case-control study of facial clefts. Birth Defects Res A Clin Mol Teratol. 2005 Aug;73(8):541-6. PubMed
Liu W, Selever J, Murali D, Sun X, Brugger SM, Ma L, Schwartz RJ, Maxson R, Furuta Y, Martin JF. Threshold-specific requirements for Bmp4 in mandibular development. Dev Biol. 2005 Jul 15;283(2):282-93. PubMed
Lallemand Y, Nicola MA, Ramos C, Bach A, Cloment CS, Robert B. Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development. Development. 2005 Jul;132(13):3003-14. Epub 2005 Jun 1. PubMed PMID: 15930102.
Sakai D, Wakamatsu Y. [Regulatory mechanisms for neural crest formation]. Tanpakushitsu Kakusan Koso. 2005 May;50(6 Suppl):684-91. Review. Japanese. PubMed
Larmour CJ, Mossey PA, Thind BS, Forgie AH, Stirrups DR. Hypodontia--a retrospective review of prevalence and etiology. Part I. Quintessence Int. 2005 Apr;36(4):263-70. Review. PubMed
Yamamoto H, Cho SW, Song SJ, Hwang HJ, Lee MJ, Kim JY, Jung HS. Characteristic tissue interaction of the diastema region in mice. Arch Oral Biol. 2005 Feb;50(2):189-98. PubMed
Ogi H, Suzuki K, Ogino Y, Kamimura M, Miyado M, Ying X, Zhang Z, Shinohara M, Chen Y, Yamada G. Ventral abdominal wall dysmorphogenesis of Msx1/Msx2 double-mutant mice. Anat Rec A Discov Mol Cell Evol Biol. 2005 May;284(1):424-30. PubMed
Givens ML, Rave-Harel N, Goonewardena VD, Kurotani R, Berdy SE, Swan CH, Rubenstein JL, Robert B, Mellon PL. Developmental regulation of gonadotropin-releasing hormone gene expression by the MSX and DLX homeodomain protein families. J Biol Chem. 2005 May 13;280(19):19156-65. Epub 2005 Mar 1. PubMed
Priam F, Ronco V, Locker M, Bourd K, Bonnefoix M, Duchne T, Bitard J, Wurtz T, Kellermann O, Goldberg M, Poliard A. New cellular models for tracking the odontoblast phenotype. Arch Oral Biol. 2005 Feb;50(2):271-7. Epub 2004 Dec 15. PubMed
Ogawa T, Kapadia H, Wang B, D'Souza RN. Studies on Pax9-Msx1 protein interactions. Arch Oral Biol. 2005 Feb;50(2):141-5. Epub 2005 Jan 28. PubMed
Liu W, Sun X, Braut A, Mishina Y, Behringer RR, Mina M, Martin JF. Distinct functions for Bmp signaling in lip and palate fusion in mice. Development. 2005 Mar;132(6):1453-61. Epub 2005 Feb 16. PubMed
Park K, Kim K, Rho SB, Choi K, Kim D, Oh SH, Park J, Lee SH, Lee JH. Homeobox Msx1 interacts with p53 tumor suppressor and inhibits tumor growth by inducing apoptosis. Cancer Res. 2005 Feb 1;65(3):749-57. PubMed
Hyckel P, Berndt A, Schleier P, Clement JH, Beensen V, Peters H, Kosmehl H. Cherubism - new hypotheses on pathogenesis and therapeutic consequences. J Craniomaxillofac Surg. 2005 Feb;33(1):61-8. Epub 2005 Jan 12. PubMed PMID: 15694152.
Monsoro-Burq AH, Wang E, Harland R. Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction. Dev Cell. 2005 Feb;8(2):167-78. PubMed
Matsui H, Takahashi T, Raghow R. The mechanism of biogenesis and potential function of the two alternatively spliced mRNAs encoded by the murine Msx3 gene. Mol Cell Biochem. 2004 Dec;267(1-2):1-11. PubMed
Klein ML, Nieminen P, Lammi L, Niebuhr E, Kreiborg S. Novel mutation of the initiation codon of PAX9 causes oligodontia. J Dent Res. 2005 Jan;84(1):43-7. PubMed
Kettunen P, Les S, Furmanek T, Fjeld K, Kvinnsland IH, Behar O, Yagi T, Fujisawa H, Vainio S, Taniguchi M, Luukko K. Coordination of trigeminal axon navigation and patterning with tooth organ formation
Song Y, Hui JN, Fu KK, Richman JM. Control of retinoic acid synthesis and FGF expression in the nasal pit is required to pattern the craniofacial skeleton. Dev Biol. 2004 Dec 15;276(2):313-29. PubMed
Schnapp E, Tanaka EM. Quantitative evaluation of morpholino-mediated protein knockdown of GFP, MSX1, and PAX7 during tail regeneration in Ambystoma mexicanum. Dev Dyn. 2005 Jan;232(1):162-70. Erratum in
Kolenc-Fus FJ. Tooth agenesis
Trbulo C, Aybar MJ, Snchez SS, Mayor R. A balance between the anti-apoptotic activity of Slug and the apoptotic activity of msx1 is required for the proper development of the neural crest. Dev Biol. 2004 Nov 15;275(2):325-42. PubMed
Wong FK, Hagg U. An update on the aetiology of orofacial clefts. Hong Kong Med J. 2004 Oct;10(5):331-6. Review. PubMed
Burstyn-Cohen T, Stanleigh J, Sela-Donenfeld D, Kalcheim C. Canonical Wnt activity regulates trunk neural crest delamination linking BMP/noggin signaling with G1/S transition. Development. 2004 Nov;131(21):5327-39. Epub 2004 Sep 29. PubMed
Kolterud A, Alenius M, Carlsson L, Bohm S. The Lim homeobox gene Lhx2 is required for olfactory sensory neuron identity. Development. 2004 Nov;131(21):5319-26. Epub 2004 Sep 29. PubMed
Fux C, Langer D, Fussenegger M. Dual-regulated myoD- and msx1-based interventions in C2C12-derived cells enable precise myogenic/osteogenic/adipogenic lineage control. J Gene Med. 2004 Oct;6(10):1159-69. PubMed
Suazo J, Santos JL, Carreo H, Jara L, Blanco R. Linkage disequilibrium between MSX1 and non-syndromic cleft lip/palate in the Chilean population. J Dent Res. 2004 Oct;83(10):782-5. PubMed
Vieira AR, Castillo Taucher S, Aravena T, Astete C, Sanz P, Tastets ME, Monasterio L, Murray JC. [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]. Rev Med Chil. 2004 Jul;132(7):816-22. Spanish. PubMed
Field LL, Ray AK, Cooper ME, Goldstein T, Shaw DF, Marazita ML. Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India. Am J Med Genet A. 2004 Oct 15;130A(3):265-71. PubMed
Suzuki Y, Jezewski PA, Machida J, Watanabe Y, Shi M, Cooper ME, Viet le T, Nguyen TD, Hai H, Natsume N, Shimozato K, Marazita ML, Murray JC. In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genet Med. 2004 May-Jun;6(3):117-25. PubMed
Vieira AR, Meira R, Modesto A, Murray JC. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. J Dent Res. 2004 Sep;83(9):723-7. PubMed PMID: 15329380.
Odelberg SJ. Unraveling the molecular basis for regenerative cellular plasticity. PLoS Biol. 2004 Aug;2(8):E232. Epub 2004 Aug 17. Review. PubMed PMID: 15314652; PubMed Central PMCID
Kumar A, Velloso CP, Imokawa Y, Brockes JP. The regenerative plasticity of isolated urodele myofibers and its dependence on MSX1. PLoS Biol. 2004 Aug;2(8):E218. Epub 2004 Aug 17. PubMed
Ramos C, Martinez A, Robert B, Soriano E. Msx1 expression in the adult mouse brain
Vi-Fane B, Nefussi JR, Orestes-Cardoso S, Hotton D, Robert B, Chabre C, Berdal A, Davideau JL. [Genetic and experimental approach to bony craniofacial growth
Satoh K, Ginsburg E, Vonderhaar BK. Msx-1 and Msx-2 in mammary gland development. J Mammary Gland Biol Neoplasia. 2004 Apr;9(2):195-205. Review. PubMed
Kuwajima T, Taniura H, Nishimura I, Yoshikawa K. Necdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cells. J Biol Chem. 2004 Sep 24;279(39):40484-93. Epub 2004 Jul 21. PubMed
Fliniaux I, Viallet JP, Dhouailly D. Signaling dynamics of feather tract formation from the chick somatopleure. Development. 2004 Aug;131(16):3955-66. Epub 2004 Jul 21. PubMed
De Muynck S, Schollen E, Matthijs G, Verdonck A, Devriendt K, Carels C. A novel MSX1 mutation in hypodontia. Am J Med Genet A. 2004 Aug 1;128A(4):401-3. PubMed
Gajavelli S, Wood PM, Pennica D, Whittemore SR, Tsoulfas P. BMP signaling initiates a neural crest differentiation program in embryonic rat CNS stem cells. Exp Neurol. 2004 Aug;188(2):205-23. PubMed
Braam B, de Roos R, Dijk A, Boer P, Post JA, Kemmeren PP, Holstege FC, Bluysen HA, Koomans HA. Nitric oxide donor induces temporal and dose-dependent reduction of gene expression in human endothelial cells. Am J Physiol Heart Circ Physiol. 2004 Nov;287(5):H1977-86. Epub 2004 Jul 8. PubMed
Kaartinen V, Dudas M, Nagy A, Sridurongrit S, Lu MM, Epstein JA. Cardiac outflow tract defects in mice lacking ALK2 in neural crest cells. Development. 2004 Jul;131(14):3481-90. PubMed
Lzot F, Coudert A, Petit S, Vi-Fane B, Hotton D, Davideau JL, Kato S, Descroix V, Pibouin L, Berdal A. Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA? J Steroid Biochem Mol Biol. 2004 May;89-90(1-5):413-7. PubMed
Schlosser G, Ahrens K. Molecular anatomy of placode development in Xenopus laevis. Dev Biol. 2004 Jul 15;271(2):439-66. PubMed
Ohazama A, Modino SA, Miletich I, Sharpe PT. Stem-cell-based tissue engineering of murine teeth. J Dent Res. 2004 Jul;83(7):518-22. PubMed PMID: 15218039.
Fernndez-Llebrez P, Grondona JM, Prez J, Lpez-Aranda MF, Estivill-Torrs G, Llebrez-Zayas PF, Soriano E, Ramos C, Lallemand Y, Bach A, Robert B. Msx1-deficient mice fail to form prosomere 1 derivatives, subcommissural organ, and posterior commissure and develop hydrocephalus. J Neuropathol Exp Neurol. 2004 Jun;63(6):574-86. PubMed
Lee H, Habas R, Abate-Shen C. MSX1 cooperates with histone H1b for inhibition of transcription and myogenesis. Science. 2004 Jun 11;304(5677):1675-8. PubMed
Cirillo L, Zaret K. Developmental biology. A linker histone restricts muscle development. Science. 2004 Jun 11;304(5677):1607-9. PubMed
Ramos C, Fernndez-Llebrez P, Bach A, Robert B, Soriano E. Msx1 disruption leads to diencephalon defects and hydrocephalus. Dev Dyn. 2004 Jul;230(3):446-60. PubMed
Aberg T, Wang XP, Kim JH, Yamashiro T, Bei M, Rice R, Ryoo HM, Thesleff I. Runx2 mediates FGF signaling from epithelium to mesenchyme during tooth morphogenesis. Dev Biol. 2004 Jun 1;270(1):76-93. PubMed
Andl T, Ahn K, Kairo A, Chu EY, Wine-Lee L, Reddy ST, Croft NJ, Cebra-Thomas JA, Metzger D, Chambon P, Lyons KM, Mishina Y, Seykora JT, Crenshaw EB 3rd, Millar SE. Epithelial Bmpr1a regulates differentiation and proliferation in postnatal hair follicles and is essential for tooth development. Development. 2004 May;131(10):2257-68. Epub 2004 Apr 21. PubMed
Kruzynska-Frejtag A, Wang J, Maeda M, Rogers R, Krug E, Hoffman S, Markwald RR, Conway SJ. Periostin is expressed within the developing teeth at the sites of epithelial-mesenchymal interaction. Dev Dyn. 2004 Apr;229(4):857-68. PubMed PMID: 15042709.
Djouss L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, Gmez-Tortosa E, Mayo Cabrero D, Jones R, Zanko A, Nance M, Abramson RK, Suchowersky O, Paulsen JS, Harrison MB, Yang Q, Cupples LA, Mysore J, Gusella JF, MacDonald ME, Myers RH. Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics. 2004 Jun;5(2):109-14. Epub 2004 Mar 17. PubMed
Carmichael SL, Shaw GM, Yang W, Lammer EJ, Zhu H, Finnell RH. Limb deficiency defects, MSX1, and exposure to tobacco smoke. Am J Med Genet A. 2004 Mar 15;125A(3):285-9. PubMed
Blanco R, Suazo J, Santos JL, Paredes M, Sung H, Carreo H, Jara L. Association between 10 microsatellite markers and nonsyndromic cleft lip palate in the Chilean population. Cleft Palate Craniofac J. 2004 Mar;41(2):163-7. PubMed
Moreno LM, Arcos-Burgos M, Marazita ML, Krahn K, Maher BS, Cooper ME, Valencia-Ramirez CR, Lidral AC. Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio. Am J Med Genet A. 2004 Mar 1;125A(2):135-44. PubMed
Daikoku T, Song H, Guo Y, Riesewijk A, Mosselman S, Das SK, Dey SK. Uterine Msx-1 and Wnt4 signaling becomes aberrant in mice with the loss of leukemia inhibitory factor or Hoxa-10
Liu Y, Helms AW, Johnson JE. Distinct activities of Msx1 and Msx3 in dorsal neural tube development. Development. 2004 Mar;131(5):1017-28. PubMed PMID: 14973289.
Cox TC. Taking it to the max
Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. Am J Med Genet A. 2004 Feb 15;125A(1):17-22. PubMed
Alappat S, Zhang ZY, Chen YP. Msx homeobox gene family and craniofacial development. Cell Res. 2003 Dec;13(6):429-42. Review. PubMed
Ma L, Chen Z, Song GT, Fan MW, Zhang Q, Wang ZF. [Expression of homeobox gene Msx-1, Msx-2 and Dlx-2 during murine mandibular first molar development]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2003 Nov;38(6):429-31. Chinese. PubMed PMID: 14703475.
Zhang Z, Song Y, Zhang X, Tang J, Chen J, Chen Y. Msx1/Bmp4 genetic pathway regulates mammalian alveolar bone formation via induction of Dlx5 and Cbfa1. Mech Dev. 2003 Dec;120(12):1469-79. PubMed
Bottone FG Jr, Martinez JM, Alston-Mills B, Eling TE. Gene modulation by Cox-1 and Cox-2 specific inhibitors in human colorectal carcinoma cancer cells. Carcinogenesis. 2004 Mar;25(3):349-57. Epub 2003 Nov 21. PubMed
Nieminen P, Kotilainen J, Aalto Y, Knuutila S, Pirinen S, Thesleff I. MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia. J Dent Res. 2003 Dec;82(12):1013-7. PubMed
Tribulo C, Aybar MJ, Nguyen VH, Mullins MC, Mayor R. Regulation of Msx genes by a Bmp gradient is essential for neural crest specification. Development. 2003 Dec;130(26):6441-52. Epub 2003 Nov 19. PubMed
Gorivodsky M, Lonai P. Novel roles of Fgfr2 in AER differentiation and positioning of the dorsoventral limb interface. Development. 2003 Nov;130(22):5471-9. Epub 2003 Sep 24. PubMed
Mostowska A, Kobielak A, Trzeciak WH. Molecular basis of non-syndromic tooth agenesis
Beck CW, Christen B, Slack JM. Molecular pathways needed for regeneration of spinal cord and muscle in a vertebrate. Dev Cell. 2003 Sep;5(3):429-39. PubMed
Hamrick MW. Evolution and development of mammalian limb integumentary structures. J Exp Zool B Mol Dev Evol. 2003 Aug 15;298(1):152-63. Review. PubMed
Han M, Yang X, Farrington JE, Muneoka K. Digit regeneration is regulated by Msx1 and BMP4 in fetal mice. Development. 2003 Nov;130(21):5123-32. Epub 2003 Aug 27. PubMed
Han J, Ito Y, Yeo JY, Sucov HM, Maas R, Chai Y. Cranial neural crest-derived mesenchymal proliferation is regulated by Msx1-mediated p19(INK4d) expression during odontogenesis. Dev Biol. 2003 Sep 1;261(1):183-96. PubMed
Stevens CB, Davies AL, Battista S, Lewis JH, Fekete DM. Forced activation of Wnt signaling alters morphogenesis and sensory organ identity in the chicken inner ear. Dev Biol. 2003 Sep 1;261(1):149-64. PubMed
Fallin MD, Hetmanski JB, Park J, Scott AF, Ingersoll R, Fuernkranz HA, McIntosh I, Beaty TH. Family-based analysis of MSX1 haplotypes for association with oral clefts. Genet Epidemiol. 2003 Sep;25(2):168-75. PubMed
Vincent C, Bontoux M, Le Douarin NM, Pieau C, Monsoro-Burq AH. Msx genes are expressed in the carapacial ridge of turtle shell
Mitsiadis TA, Angeli I, James C, Lendahl U, Sharpe PT. Role of Islet1 in the patterning of murine dentition. Development. 2003 Sep;130(18):4451-60. PubMed
Bach A, Lallemand Y, Nicola MA, Ramos C, Mathis L, Maufras M, Robert B. Msx1 is required for dorsal diencephalon patterning. Development. 2003 Sep;130(17):4025-36. PubMed
Campbell EM, Nonneman D, Rohrer GA. Fine mapping a quantitative trait locus affecting ovulation rate in swine on chromosome 8. J Anim Sci. 2003 Jul;81(7):1706-14. PubMed
McLarren KW, Litsiou A, Streit A. DLX5 positions the neural crest and preplacode region at the border of the neural plate. Dev Biol. 2003 Jul 1;259(1):34-47. PubMed
Kiyono M, Shibuya M. Bone morphogenetic protein 4 mediates apoptosis of capillary endothelial cells during rat pupillary membrane regression. Mol Cell Biol. 2003 Jul;23(13):4627-36. PubMed
Koillinen H, Ollikainen V, Rautio J, Hukki J, Kere J. Linkage and linkage disequilibrium searched for between non-syndromic cleft palate and four candidate loci. J Med Genet. 2003 Jun;40(6):464-8. PubMed
Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC. Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. J Med Genet. 2003 Jun;40(6):399-407. PubMed
Mostowska A, Kobielak A, Biedziak B, Trzeciak WH. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia. Eur J Oral Sci. 2003 Jun;111(3):272-6. PubMed
Wu LY, Li M, Hinton DR, Guo L, Jiang S, Wang JT, Zeng A, Xie JB, Snead M, Shuler C, Maxson RE Jr, Liu YH. Microphthalmia resulting from MSX2-induced apoptosis in the optic vesicle. Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2404-12. PubMed
Chai Y, Ito Y, Han J. TGF-beta signaling and its functional significance in regulating the fate of cranial neural crest cells. Crit Rev Oral Biol Med. 2003;14(2):78-88. Review. PubMed
Line SR. Variation of tooth number in mammalian dentition
Butler SJ, Dodd J. A role for BMP heterodimers in roof plate-mediated repulsion of commissural axons. Neuron. 2003 May 8;38(3):389-401. PubMed PMID: 12741987.
Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ. Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. Cleft Palate Craniofac J. 2003 May;40(3):274-9. PubMed PMID: 12733956; PubMed Central PMCID
Zhao H, Cao Y, Grunz H. Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway. Dev Biol. 2003 May 15;257(2):278-91. PubMed
Holleville N, Quilhac A, Bontoux M, Monsoro-Burq AH. BMP signals regulate Dlx5 during early avian skull development. Dev Biol. 2003 May 1;257(1):177-89. PubMed
Shibaguchi T, Kato J, Abe M, Tamamura Y, Tabata MJ, Liu JG, Iwamoto M, Wakisaka S, Wanaka A, Kurisu K. Expression and role of Lhx8 in murine tooth development. Arch Histol Cytol. 2003 Mar;66(1):95-108. PubMed
Zhang Z, Zhang X, Avniel WA, Song Y, Jones SM, Jones TA, Fermin C, Chen Y. Malleal processus brevis is dispensable for normal hearing in mice. Dev Dyn. 2003 May;227(1):69-77. PubMed
Miletich I, Sharpe PT. Normal and abnormal dental development. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R69-73. Review. PubMed
Herr A, Meunier D, Mller I, Rump A, Fundele R, Ropers HH, Nuber UA. Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis. Dev Dyn. 2003 Apr;226(4):579-86. PubMed
Jugessur A, Lie RT, Wilcox AJ, Murray JC, Taylor JA, Saugstad OD, Vindenes HA, Abyholm F. Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts
Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC. MSX1 and TGFB3 contribute to clefting in South America. J Dent Res. 2003 Apr;82(4):289-92. PubMed
Ivey K, Tyson B, Ukidwe P, McFadden DG, Levi G, Olson EN, Srivastava D, Wilkie TM. Galphaq and Galpha11 proteins mediate endothelin-1 signaling in neural crest-derived pharyngeal arch mesenchyme. Dev Biol. 2003 Mar 15;255(2):230-7. PubMed
Osada S, Ohmori SY, Taira M. XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos. Development. 2003 May;130(9):1783-94. PubMed
Yamashiro T, Tummers M, Thesleff I. Expression of bone morphogenetic proteins and Msx genes during root formation. J Dent Res. 2003 Mar;82(3):172-6. PubMed
Vieira AR. Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis. J Dent Res. 2003 Mar;82(3):162-5. Review. PubMed
Zollino M, Lecce R, Fischetto R, Murdolo M, Faravelli F, Selicorni A, Butt C, Memo L, Capovilla G, Neri G. Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2. Am J Hum Genet. 2003 Mar;72(3):590-7. Epub 2003 Jan 30. PubMed
Payton A, Holland F, Diggle P, Rabbitt P, Horan M, Davidson Y, Gibbons L, Worthington J, Ollier WE, Pendleton N. Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population. Mol Psychiatry. 2003 Jan;8(1):14-8. PubMed
Peck S, Peck L, Kataja M. Concomitant occurrence of canine malposition and tooth agenesis
Orestes-Cardoso S, Nefussi JR, Lezot F, Oboeuf M, Pereira M, Mesbah M, Robert B, Berdal A. Msx1 is a regulator of bone formation during development and postnatal growth
Berdal A, Lezot F, Pibouin L, Hotton D, Ghoul-Mazgar S, Teillaud C, Robert B, MacDougall M, Blin C. Msx1 homeogene antisense mRNA in mouse dental and bone cells. Connect Tissue Res. 2002;43(2-3):148-52. PubMed
Blanc I, Bach A, Robert B. Unusual pattern of Sonic hedgehog expression in the polydactylous mouse mutant Hemimelic extra-toes. Int J Dev Biol. 2002;46(7):969-74. PubMed
Ashique AM, Fu K, Richman JM. Endogenous bone morphogenetic proteins regulate outgrowth and epithelial survival during avian lip fusion. Development. 2002 Oct;129(19):4647-60. PubMed
Zhao S, Chen Q, Hung FC, Overbeek PA. BMP signaling is required for development of the ciliary body. Development. 2002 Oct;129(19):4435-42. PubMed
Streit A. Extensive cell movements accompany formation of the otic placode. Dev Biol. 2002 Sep 15;249(2):237-54. PubMed
Guha U, Gomes WA, Kobayashi T, Pestell RG, Kessler JA. In vivo evidence that BMP signaling is necessary for apoptosis in the mouse limb. Dev Biol. 2002 Sep 1;249(1):108-20. PubMed
Zhang Z, Song Y, Zhao X, Zhang X, Fermin C, Chen Y. Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis. Development. 2002 Sep;129(17):4135-46. PubMed
Hecht JT, Mulliken JB, Blanton SH. Evidence for a cleft palate only locus on chromosome 4 near MSX1. Am J Med Genet. 2002 Jul 15;110(4):406-7. PubMed PMID: 12116220.
Lidral AC, Reising BC. The role of MSX1 in human tooth agenesis. J Dent Res. 2002 Apr;81(4):274-8. PubMed
Willert J, Epping M, Pollack JR, Brown PO, Nusse R. A transcriptional response to Wnt protein in human embryonic carcinoma cells. BMC Dev Biol. 2002 Jul 2;2:8. PubMed
Timmer JR, Wang C, Niswander L. BMP signaling patterns the dorsal and intermediate neural tube via regulation of homeobox and helix-loop-helix transcription factors. Development. 2002 May;129(10):2459-72. PubMed PMID: 11973277.
Ohkubo Y, Chiang C, Rubenstein JL. Coordinate regulation and synergistic actions of BMP4, SHH and FGF8 in the rostral prosencephalon regulate morphogenesis of the telencephalic and optic vesicles. Neuroscience. 2002;111(1):1-17. PubMed
Ashique AM, Fu K, Richman JM. Signalling via type IA and type IB bone morphogenetic protein receptors (BMPR) regulates intramembranous bone formation, chondrogenesis and feather formation in the chicken embryo. Int J Dev Biol. 2002 Mar;46(2):243-53. PubMed
Mina M, Wang YH, Ivanisevic AM, Upholt WB, Rodgers B. Region- and stage-specific effects of FGFs and BMPs in chick mandibular morphogenesis. Dev Dyn. 2002 Mar;223(3):333-52. PubMed
Marazita ML, Field LL, Cooper ME, Tobias R, Maher BS, Peanchitlertkajorn S, Liu YE. Nonsyndromic cleft lip with or without cleft palate in China
Vieira AR, Orioli IM. Candidate genes for nonsyndromic cleft lip and palate. ASDC J Dent Child. 2001 Jul-Aug;68(4):272-9, 229. Review. PubMed
Alvarez Martinez CE, Binato R, Gonzalez S, Pereira M, Robert B, Abdelhay E. Characterization of a Smad motif similar to Drosophila mad in the mouse Msx 1 promoter. Biochem Biophys Res Commun. 2002 Mar 1;291(3):655-62. PubMed PMID: 11855840.
Frazier-Bowers SA, Guo DC, Cavender A, Xue L, Evans B, King T, Milewicz D, D'Souza RN. A novel mutation in human PAX9 causes molar oligodontia. J Dent Res. 2002 Feb;81(2):129-33. PubMed
Scapoli L, Martinelli M, Pezzetti F, Carinci F, Bodo M, Tognon M, Carinci P. Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate. Hum Genet. 2002 Jan;110(1):15-20. Epub 2001 Nov 10. PubMed
Beaty TH, Hetmanski JB, Zeiger JS, Fan YT, Liang KY, VanderKolk CA, McIntosh I. Testing candidate genes for non-syndromic oral clefts using a case-parent trio design. Genet Epidemiol. 2002 Jan;22(1):1-11. PubMed
Spritz RA. The genetics and epigenetics of orofacial clefts. Curr Opin Pediatr. 2001 Dec;13(6):556-60. Review. PubMed
McGonnell IM, Green CR, Tickle C, Becker DL. Connexin43 gap junction protein plays an essential role in morphogenesis of the embryonic chick face. Dev Dyn. 2001 Nov;222(3):420-38. PubMed
Scaal M, Prls F, Fchtbauer EM, Patel K, Hornik C, Khler T, Christ B, Brand-Saberi B. BMPs induce dermal markers and ectopic feather tracts. Mech Dev. 2002 Jan;110(1-2):51-60. PubMed
Pearson H. The regeneration gap. Nature. 2001 Nov 22;414(6862):388-90. PubMed
Wang Y, Wang J, Gao Y. [Comparative study of expression of homeobox gene Msx-1, Msx-2 mRNA during the hard tissue formation of mouse tooth development]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2001 Jul;36(4):259-61. Chinese. PubMed PMID: 11718005.
Hamrick MW. Development and evolution of the mammalian limb
Norlin EM, Alenius M, Gussing F, Hgglund M, Vedin V, Bohm S. Evidence for gradients of gene expression correlating with zonal topography of the olfactory sensory map. Mol Cell Neurosci. 2001 Sep;18(3):283-95. PubMed
Hovde S, Abate-Shen C, Geiger JH. Crystal structure of the Msx-1 homeodomain/DNA complex. Biochemistry. 2001 Oct 9;40(40):12013-21. PubMed PMID: 11580277.
Yamamoto TS, Takagi C, Hyodo AC, Ueno N. Suppression of head formation by Xmsx-1 through the inhibition of intracellular nodal signaling. Development. 2001 Jul;128(14):2769-79. PubMed
Gong SG. Phenotypic and molecular analyses of A/WySn mice. Cleft Palate Craniofac J. 2001 Sep;38(5):486-91. PubMed
Bushdid PB, Chen CL, Brantley DM, Yull F, Raghow R, Kerr LD, Barnett JV. NF-kappaB mediates FGF signal regulation of msx-1 expression. Dev Biol. 2001 Sep 1;237(1):107-15. PubMed
Hu G, Lee H, Price SM, Shen MM, Abate-Shen C. Msx homeobox genes inhibit differentiation through upregulation of cyclin D1. Development. 2001 Jun;128(12):2373-84. PubMed
Mina M. Morphogenesis of the medial region of the developing mandible is regulated by multiple signaling pathways. Cells Tissues Organs. 2001;169(3):295-301. Review. PubMed
Beaty TH, Wang H, Hetmanski JB, Fan YT, Zeiger JS, Liang KY, Chiu YF, Vanderkolk CA, Seifert KC, Wulfsberg EA, Raymond G, Panny SR, McIntosh I. A case-control study of nonsyndromic oral clefts in Maryland. Ann Epidemiol. 2001 Aug;11(6):434-42. PubMed
Line SR. Molecular morphogenetic fields in the development of human dentition. J Theor Biol. 2001 Jul 7;211(1):67-75. PubMed
Blin-Wakkach C, Lezot F, Ghoul-Mazgar S, Hotton D, Monteiro S, Teillaud C, Pibouin L, Orestes-Cardoso S, Papagerakis P, Macdougall M, Robert B, Berdal A. Endogenous Msx1 antisense transcript
Mitchell LE, Murray JC, O'Brien S, Christensen K. Evaluation of two putative susceptibility loci for oral clefts in the Danish population. Am J Epidemiol. 2001 May 15;153(10):1007-15. PubMed
Kobielak A, Kobielak K, Wiśniewski AS, Mostowska A, Biedziak B, Trzeciak WH. The novel polymorphic variants within the paired box of the PAX9 gene are associated with selective tooth agenesis. Folia Histochem Cytobiol. 2001;39(2):111-2. Review. PubMed
Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet. 2001 Jul;69(1):67-74. Epub 2001 May 16. PubMed
Orestes-Cardoso SM, Nefussi JR, Hotton D, Mesbah M, Orestes-Cardoso MD, Robert B, Berdal A. Postnatal Msx1 expression pattern in craniofacial, axial, and appendicular skeleton of transgenic mice from the first week until the second year. Dev Dyn. 2001 May;221(1):1-13. PubMed
Alavizadeh A, Kiernan AE, Nolan P, Lo C, Steel KP, Bucan M. The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects. Dev Biol. 2001 Jun 1;234(1):244-60. PubMed
Blanco R, Chakraborty R, Barton SA, Carreo H, Paredes M, Jara L, Palomino H, Schull WJ. Evidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean population. Hum Biol. 2001 Feb;73(1):81-9. PubMed
Yokoyama H, Ide H, Tamura K. FGF-10 stimulates limb regeneration ability in Xenopus laevis. Dev Biol. 2001 May 1;233(1):72-9. PubMed
Salas-Vidal E, Valencia C, Covarrubias L. Differential tissue growth and patterns of cell death in mouse limb autopod morphogenesis. Dev Dyn. 2001 Apr;220(4):295-306. PubMed
Hughes SM. Muscle development
Park J, Park K, Kim S, Lee JH. Msx1 gene overexpression induces G1 phase cell arrest in human ovarian cancer cell line OVCAR3. Biochem Biophys Res Commun. 2001 Mar;281(5):1234-40. PubMed
Revest JM, Spencer-Dene B, Kerr K, De Moerlooze L, Rosewell I, Dickson C. Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 and is required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4. Dev Biol. 2001 Mar 1;231(1):47-62. PubMed
Odelberg SJ, Kollhoff A, Keating MT. Dedifferentiation of mammalian myotubes induced by msx1. Cell. 2000 Dec 22;103(7):1099-109. PubMed
Trousse F, Esteve P, Bovolenta P. Bmp4 mediates apoptotic cell death in the developing chick eye. J Neurosci. 2001 Feb 15;21(4):1292-301. PubMed PMID: 11160400; PubMed Central PMCID
Endo T, Tamura K, Ide H. Analysis of gene expressions during Xenopus forelimb regeneration. Dev Biol. 2000 Apr 15;220(2):296-306. PubMed PMID: 10753517.
Mehra-Chaudhary R, Matsui H, Raghow R. Msx3 protein recruits histone deacetylase to down-regulate the Msx1 promoter. Biochem J. 2001 Jan 1;353(Pt 1):13-22. PubMed
Lu CH, Rincn-Limas DE, Botas J. Conserved overlapping and reciprocal expression of msh/Msx1 and apterous/Lhx2 in Drosophila and mice. Mech Dev. 2000 Dec;99(1-2):177-81. PubMed
Zhao X, Zhang Z, Song Y, Zhang X, Zhang Y, Hu Y, Fromm SH, Chen Y. Transgenically ectopic expression of Bmp4 to the Msx1 mutant dental mesenchyme restores downstream gene expression but represses Shh and Bmp2 in the enamel knot of wild type tooth germ. Mech Dev. 2000 Dec;99(1-2):29-38. PubMed
Shigetani Y, Nobusada Y, Kuratani S. Ectodermally derived FGF8 defines the maxillomandibular region in the early chick embryo
Eggenschwiler JT, Anderson KV. Dorsal and lateral fates in the mouse neural tube require the cell-autonomous activity of the open brain gene. Dev Biol. 2000 Nov 15;227(2):648-60. PubMed
Bryan JT, Morasso MI. The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1. J Cell Sci. 2000 Nov;113 ( Pt 22):4013-23. PubMed
Bei M, Kratochwil K, Maas RL. BMP4 rescues a non-cell-autonomous function of Msx1 in tooth development. Development. 2000 Nov;127(21):4711-8. PubMed PMID: 11023873.
Goldenberg M, Das P, Messersmith M, Stockton DW, Patel PI, D'Souza RN. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia. J Dent Res. 2000 Jul;79(7):1469-75. PubMed
Christ B, Huang R, Wilting J. The development of the avian vertebral column. Anat Embryol (Berl). 2000 Sep;202(3):179-94. Review. PubMed
Ishimura A, Maeda R, Takeda M, Kikkawa M, Daar IO, Mano M. Involvement of BMP-4/msx-1 and FGF pathways in neural induction in the Xenopus embryo. Dev Growth Differ. 2000 Aug;42(4):307-16. PubMed
Chen Y, Zhang Y, Jiang TX, Barlow AJ, St Amand TR, Hu Y, Heaney S, Francis-West P, Chuong CM, Maas R. Conservation of early odontogenic signaling pathways in Aves. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10044-9. PubMed
Thompson-Jaeger S, Raghow R. Exogenous expression of Msx1 renders myoblasts refractory to differentiation into myotubes and elicits enhanced biosynthesis of four unique mRNAs. Mol Cell Biochem. 2000 May;208(1-2):63-9. PubMed PMID: 10939629.
Cornelison DD, Olwin BB, Rudnicki MA, Wold BJ. MyoD(-/-) satellite cells in single-fiber culture are differentiation defective and MRF4 deficient. Dev Biol. 2000 Aug 15;224(2):122-37. PubMed
Beanan MJ, Sargent TD. Regulation and function of Dlx3 in vertebrate development. Dev Dyn. 2000 Aug;218(4):545-53. Review. PubMed
Cohen MM Jr. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2. J Craniofac Genet Dev Biol. 2000 Jan-Mar;20(1):19-25. Review. PubMed
Takeda M, Saito Y, Sekine R, Onitsuka I, Maeda R, Mano M. Xenopus msx-1 regulates dorso-ventral axis formation by suppressing the expression of organizer genes. Comp Biochem Physiol B Biochem Mol Biol. 2000 Jun;126(2):157-68. PubMed
Steadman DJ, Giuffrida D, Gelmann EP. DNA-binding sequence of the human prostate-specific homeodomain protein NKX3.1. Nucleic Acids Res. 2000 Jun 15;28(12):2389-95. PubMed
Scarel RM, Trevilatto PC, Di Hiplito O Jr, Camargo LE, Line SR. Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia. Am J Med Genet. 2000 Jun 19;92(5):346-9. PubMed
Carreo H, Paredes M, Tllez G, Palomino H, Blanco R. [Association of non-syndromic cleft lip and cleft palate with microsatellite markers located in 6p]. Rev Med Chil. 1999 Oct;127(10):1189-98. Spanish. PubMed
Haraguchi R, Suzuki K, Murakami R, Sakai M, Kamikawa M, Kengaku M, Sekine K, Kawano H, Kato S, Ueno N, Yamada G. Molecular analysis of external genitalia formation
Houzelstein D, Chraud Y, Auda-Boucher G, Fontaine-Prus J, Robert B. The expression of the homeobox gene Msx1 reveals two populations of dermal progenitor cells originating from the somites. Development. 2000 May;127(10):2155-64. PubMed
Lzot F, Thomas B, Hotton D, Forest N, Orestes-Cardoso S, Robert B, Sharpe P, Berdal A. Biomineralization, life-time of odontogenic cells and differential expression of the two homeobox genes MSX-1 and DLX-2 in transgenic mice. J Bone Miner Res. 2000 Mar;15(3):430-41. PubMed
Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet. 2000 Apr;24(4):391-5. PubMed
van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet. 2000 Apr;24(4):342-3. Erratum in
Ferguson MW. A hole in the head. Nat Genet. 2000 Apr;24(4):330-1. PubMed
Holme RH, Thomson SJ, Davidson DR. Ectopic expression of Msx2 in chick retinal pigmented epithelium cultures suggests a role in patterning the optic vesicle. Mech Dev. 2000 Mar 1;91(1-2):175-87. PubMed
Yamamoto TS, Takagi C, Ueno N. Requirement of Xmsx-1 in the BMP-triggered ventralization of Xenopus embryos. Mech Dev. 2000 Mar 1;91(1-2):131-41. PubMed
Zhang Y, Zhang Z, Zhao X, Yu X, Hu Y, Geronimo B, Fromm SH, Chen YP. A new function of BMP4
Ngo-Muller V, Muneoka K. Influence of FGF4 on digit morphogenesis during limb development in the mouse. Dev Biol. 2000 Mar 15;219(2):224-36. PubMed
DeWees S, Geiger JH. Structural studies of the Msx-1 homeodomain-DNA complex I. Acta Crystallogr D Biol Crystallogr. 1999 Dec;55(Pt 12):2039-40. PubMed
Wang YH, Rutherford B, Upholt WB, Mina M. Effects of BMP-7 on mouse tooth mesenchyme and chick mandibular mesenchyme. Dev Dyn. 1999 Dec;216(4-5):320-35. PubMed
St Amand TR, Zhang Y, Semina EV, Zhao X, Hu Y, Nguyen L, Murray JC, Chen Y. Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage. Dev Biol. 2000 Jan 15;217(2):323-32. PubMed
Ferguson CA, Tucker AS, Sharpe PT. Temporospatial cell interactions regulating mandibular and maxillary arch patterning. Development. 2000 Jan;127(2):403-12. PubMed
Chang W, Nunes FD, De Jesus-Escobar JM, Harland R, Wu DK. Ectopic noggin blocks sensory and nonsensory organ morphogenesis in the chicken inner ear. Dev Biol. 1999 Dec 1;216(1):369-81. PubMed
Heymer J, Rther U. Syndactyly of Ft/+ mice correlates with an imbalance in bmp4 and fgf8 expression. Mech Dev. 1999 Nov;88(2):173-81. PubMed
Bendall AJ, Ding J, Hu G, Shen MM, Abate-Shen C. Msx1 antagonizes the myogenic activity of Pax3 in migrating limb muscle precursors. Development. 1999 Nov;126(22):4965-76. PubMed
Kuratani S, Satokata I, Blum M, Komatsu Y, Haraguchi R, Nakamura S, Suzuki K, Kosai K, Maas R, Yamada G. Middle ear defects associated with the double knock out mutation of murine goosecoid and Msx1 genes. Cell Mol Biol (Noisy-le-grand). 1999 Jul;45(5):589-99. PubMed
Feledy JA, Beanan MJ, Sandoval JJ, Goodrich JS, Lim JH, Matsuo-Takasaki M, Sato SM, Sargent TD. Inhibitory patterning of the anterior neural plate in Xenopus by homeodomain factors Dlx3 and Msx1. Dev Biol. 1999 Aug 15;212(2):455-64. PubMed
Kernen SV, Kettunen P, Aberg T, Thesleff I, Jernvall J. Gene expression patterns associated with suppression of odontogenesis in mouse and vole diastema regions. Dev Genes Evol. 1999 Aug;209(8):495-506. PubMed
Theil T, Alvarez-Bolado G, Walter A, Rther U. Gli3 is required for Emx gene expression during dorsal telencephalon development. Development. 1999 Aug;126(16):3561-71. PubMed
Hollnagel A, Oehlmann V, Heymer J, Rther U, Nordheim A. Id genes are direct targets of bone morphogenetic protein induction in embryonic stem cells. J Biol Chem. 1999 Jul 9;274(28):19838-45. PubMed
Yamagishi T, Nakajima Y, Miyazono K, Nakamura H. Bone morphogenetic protein-2 acts synergistically with transforming growth factor-beta3 during endothelial-mesenchymal transformation in the developing chick heart. J Cell Physiol. 1999 Jul;180(1):35-45. PubMed
Streit A, Stern CD. Establishment and maintenance of the border of the neural plate in the chick
Zhang Y, Zhao X, Hu Y, St Amand T, Zhang M, Ramamurthy R, Qiu M, Chen Y. Msx1 is required for the induction of Patched by Sonic hedgehog in the mammalian tooth germ. Dev Dyn. 1999 May;215(1):45-53. PubMed
Ishiguro S. [Molecular cloning, expression of rat Msx-1 and Msx-2 during early embryo genesis and roles for mandibular chondrogenesis]. Kokubyo Gakkai Zasshi. 1999 Mar;66(1):33-45. Japanese. PubMed
Houzelstein D, Auda-Boucher G, Chraud Y, Rouaud T, Blanc I, Tajbakhsh S, Buckingham ME, Fontaine-Prus J, Robert B. The homeobox gene Msx1 is expressed in a subset of somites, and in muscle progenitor cells migrating into the forelimb. Development. 1999 Jun;126(12):2689-701. PubMed
Shetty S, Takahashi T, Matsui H, Ayengar R, Raghow R. Transcriptional autorepression of Msx1 gene is mediated by interactions of Msx1 protein with a multi-protein transcriptional complex containing TATA-binding protein, Sp1 and cAMP-response-element-binding protein-binding protein (CBP/p300). Biochem J. 1999 May 1;339 ( Pt 3):751-8. PubMed
Barlow AJ, Bogardi JP, Ladher R, Francis-West PH. Expression of chick Barx-1 and its differential regulation by FGF-8 and BMP signaling in the maxillary primordia. Dev Dyn. 1999 Apr;214(4):291-302. PubMed
Fisher PJ, Turic D, Williams NM, McGuffin P, Asherson P, Ball D, Craig I, Eley T, Hill L, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Plomin R, Owen MJ. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Hum Mol Genet. 1999 May;8(5):915-22. PubMed
Peters H, Balling R. Teeth. Where and how to make them. Trends Genet. 1999 Feb;15(2):59-65. Review. PubMed
Sarapura VD, Strouth HL, Wood WM, Gordon DF, Ridgway EC. Activation of the glycoprotein hormone alpha-subunit gene promoter in thyrotropes. Mol Cell Endocrinol. 1998 Nov 25;146(1-2):77-86. PubMed
Romitti PA, Lidral AC, Munger RG, Daack-Hirsch S, Burns TL, Murray JC. Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption
Lu MF, Cheng HT, Lacy AR, Kern MJ, Argao EA, Potter SS, Olson EN, Martin JF. Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis. Dev Biol. 1999 Jan 1;205(1):145-57. PubMed
Nugent P, Greene RM. MSX-1 gene expression and regulation in embryonic palatal tissue. In Vitro Cell Dev Biol Anim. 1998 Nov-Dec;34(10):831-5. PubMed
Koshiba K, Kuroiwa A, Yamamoto H, Tamura K, Ide H. Expression of Msx genes in regenerating and developing limbs of axolotl. J Exp Zool. 1998 Dec 15;282(6):703-14. PubMed
Weiss JB, Von Ohlen T, Mellerick DM, Dressler G, Doe CQ, Scott MP. Dorsoventral patterning in the Drosophila central nervous system
Blanco R, Jara L, Villaseca C, Palomino H, Carreo H. [Genetic variation of MSX1 has a sexual dimorphism in non syndromic cleft palate in the Chilean population]. Rev Med Chil. 1998 Jul;126(7):781-7. Spanish. PubMed
Towler DA, Bidder M, Latifi T, Coleman T, Semenkovich CF. Diet-induced diabetes activates an osteogenic gene regulatory program in the aortas of low density lipoprotein receptor-deficient mice. J Biol Chem. 1998 Nov 13;273(46):30427-34. PubMed
Tucker AS, Matthews KL, Sharpe PT. Transformation of tooth type induced by inhibition of BMP signaling. Science. 1998 Nov 6;282(5391):1136-8. PubMed PMID: 9804553.
Blanco R, Jara L, Villaseca MC. [Association of the genetic variation of (MSX1-7) and non syndromic cleft lip palate in Chilean subjects]. Rev Med Chil. 1998 Jun;126(6):637-45. Spanish. PubMed
Dassule HR, McMahon AP. Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth. Dev Biol. 1998 Oct 15;202(2):215-27. PubMed
Yang L, Zhang H, Hu G, Wang H, Abate-Shen C, Shen MM. An early phase of embryonic Dlx5 expression defines the rostral boundary of the neural plate. J Neurosci. 1998 Oct 15;18(20):8322-30. PubMed
Hollway GE, Mulley JC. Polymorphic variants within the homeobox gene MSX1
Bei M, Maas R. FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development. Development. 1998 Nov;125(21):4325-33. PubMed
Hu G, Vastardis H, Bendall AJ, Wang Z, Logan M, Zhang H, Nelson C, Stein S, Greenfield N, Seidman CE, Seidman JG, Abate-Shen C. Haploinsufficiency of MSX1
Peters H, Neubser A, Kratochwil K, Balling R. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev. 1998 Sep 1;12(17):2735-47. PubMed
Tucker AS, Al Khamis A, Sharpe PT. Interactions between Bmp-4 and Msx-1 act to restrict gene expression to odontogenic mesenchyme. Dev Dyn. 1998 Aug;212(4):533-9. PubMed
Kurisu K, Tabata MJ. [Hereditary diseases with tooth anomalies and their causal genes]. Kaibogaku Zasshi. 1998 Jun;73(3):201-8. Review. Japanese. PubMed
Bendall AJ, Rincn-Limas DE, Botas J, Abate-Shen C. Protein complex formation between Msx1 and Lhx2 homeoproteins is incompatible with DNA binding activity. Differentiation. 1998 Jul;63(3):151-7. PubMed
Hara K, Kimura J, Ide H. Effects of FGFs on the morphogenic potency and AER-maintenance activity of cultured progress zone cells of chick limb bud. Int J Dev Biol. 1998 May;42(4):591-9. PubMed
Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet. 1998 Aug;63(2):557-68. PubMed
Thomas T, Kurihara H, Yamagishi H, Kurihara Y, Yazaki Y, Olson EN, Srivastava D. A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme. Development. 1998 Aug;125(16):3005-14. PubMed
Gonzalez SM, Ferland LH, Robert B, Abdelhay E. Structural and functional analysis of mouse Msx1 gene promoter
Lincecum JM, Fannon A, Song K, Wang Y, Sassoon DA. Msh homeobox genes regulate cadherin-mediated cell adhesion and cell-cell sorting. J Cell Biochem. 1998 Jul 1;70(1):22-8. PubMed
Lee T, Bradley ME, Walowitz JL. Influence of promoter potency on the transcriptional effects of YY1, SRF and Msx-1 in transient transfection analysis. Nucleic Acids Res. 1998 Jul 1;26(13):3215-20. PubMed
McGonnell IM, Clarke JD, Tickle C. Fate map of the developing chick face: analysis of expansion of facial primordia and establishment of the primary palate. Dev Dyn. 1998 May;212(1):102-18. PubMed
Gaan Y, Macias D, Basco RD, Merino R, Hurle JM. Morphological diversity of the avian foot is related with the pattern of msx gene expression in the developing autopod. Dev Biol. 1998 Apr 1;196(1):33-41. PubMed
Kim HJ, Rice DP, Kettunen PJ, Thesleff I. FGF-, BMP- and Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development. Development. 1998 Apr;125(7):1241-51. PubMed PMID: 9477322.
Kanegae Y, Tavares AT, Izpisa Belmonte JC, Verma IM. Role of Rel/NF-kappaB transcription factors during the outgrowth of the vertebrate limb. Nature. 1998 Apr 9;392(6676):611-4. PubMed
Tucker AS, Markham HJ, Green P, Doherty P, Sharpe PT. A novel approach for inhibiting growth factor signalling in murine tooth development. Inhibition of FGF's. Eur J Oral Sci. 1998 Jan;106 Suppl 1:122-5. PubMed
Wang YH, Kollar EJ, Upholt WB, Mina M. EGF does not induce Msx-1 and Msx-2 in dental mesenchyme. Eur J Oral Sci. 1998 Jan;106 Suppl 1:100-3. PubMed PMID: 9541209.
Thomas BL, Sharpe PT. Patterning of the murine dentition by homeobox genes. Eur J Oral Sci. 1998 Jan;106 Suppl 1:48-54. PubMed
Hara K, Satoh K, Ide H. Apical ectodermal ridge-dependent expression of the chick 67 kDa laminin binding protein gene (cLbp) in developing limb bud. Zoolog Sci. 1997 Dec;14(6):969-78. PubMed
Kettunen P, Thesleff I. Expression and function of FGFs-4, -8, and -9 suggest functional redundancy and repetitive use as epithelial signals during tooth morphogenesis. Dev Dyn. 1998 Mar;211(3):256-68. PubMed
Hara K, Ide H. Msx1 expressing mesoderm is important for the apical ectodermal ridge (AER)-signal transfer in chick limb development. Dev Growth Differ. 1997 Dec;39(6):705-14. PubMed
Hwang SJ, Beaty TH, McIntosh I, Hefferon T, Panny SR. Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency. Am J Med Genet. 1998 Feb 3;75(4):419-23. PubMed
Howard TD, Guttmacher AE, McKinnon W, Sharma M, McKusick VA, Jabs EW. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus. Am J Hum Genet. 1997 Dec;61(6):1405-12. PubMed PMID: 9399901; PubMed Central PMCID
Wu DK, Nunes FD, Choo D. Axial specification for sensory organs versus non-sensory structures of the chicken inner ear. Development. 1998 Jan;125(1):11-20. PubMed
Stelnicki EJ, Kmves LG, Holmes D, Clavin W, Harrison MR, Adzick NS, Largman C. The human homeobox genes MSX-1, MSX-2, and MOX-1 are differentially expressed in the dermis and epidermis in fetal and adult skin. Differentiation. 1997 Oct;62(1):33-41. PubMed
Sarapura VD, Strouth HL, Gordon DF, Wood WM, Ridgway EC. Msx1 is present in thyrotropic cells and binds to a consensus site on the glycoprotein hormone alpha-subunit promoter. Mol Endocrinol. 1997 Nov;11(12):1782-94. PubMed PMID: 9369446.
Ekker M, Akimenko MA, Allende ML, Smith R, Drouin G, Langille RM, Weinberg ES, Westerfield M. Relationships among msx gene structure and function in zebrafish and other vertebrates. Mol Biol Evol. 1997 Oct;14(10):1008-22. PubMed
Fedtsova N, Turner EE. Inhibitory effects of ventral signals on the development of Brn-3.0-expressing neurons in the dorsal spinal cord. Dev Biol. 1997 Oct 1;190(1):18-31. PubMed
Takahashi T, Guron C, Shetty S, Matsui H, Raghow R. A minimal murine Msx-1 gene promoter. Organization of its cis-regulatory motifs and their role in transcriptional activation in cells in culture and in transgenic mice. J Biol Chem. 1997 Sep 5;272(36):22667-78. PubMed
Isshiki T, Takeichi M, Nose A. The role of the msh homeobox gene during Drosophila neurogenesis
Suzuki A, Ueno N, Hemmati-Brivanlou A. Xenopus msx1 mediates epidermal induction and neural inhibition by BMP4. Development. 1997 Aug;124(16):3037-44. PubMed
Fontaine-Prus J, Halgand P, Chraud Y, Rouaud T, Velasco ME, Cifuentes Diaz C, Rieger F. Mouse-chick chimera
Tribioli C, Frasch M, Lufkin T. Bapx1
Houzelstein D, Cohen A, Buckingham ME, Robert B. Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene. Mech Dev. 1997 Jul;65(1-2):123-33. PubMed
Maeda R, Kobayashi A, Sekine R, Lin JJ, Kung H, Mano M. Xmsx-1 modifies mesodermal tissue pattern along dorsoventral axis in Xenopus laevis embryo. Development. 1997 Jul;124(13):2553-60. PubMed
Marazzi G, Wang Y, Sassoon D. Msx2 is a transcriptional regulator in the BMP4-mediated programmed cell death pathway. Dev Biol. 1997 Jun 15;186(2):127-38. PubMed
Furuta Y, Piston DW, Hogan BL. Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development. Development. 1997 Jun;124(11):2203-12. PubMed
Li H, Tejero R, Monleon D, Bassolino-Klimas D, Abate-Shen C, Bruccoleri RE, Montelione GT. Homology modeling using simulated annealing of restrained molecular dynamics and conformational search calculations with CONGEN: application in predicting the three-dimensional structure of murine homeodomain Msx-1. Protein Sci. 1997 May;6(5):956-70. PubMed
Foerst-Potts L, Sadler TW. Disruption of Msx-1 and Msx-2 reveals roles for these genes in craniofacial, eye, and axial development. Dev Dyn. 1997 May;209(1):70-84. PubMed
Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen MM, Abate-Shen C. Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism. Mol Cell Biol. 1997 May;17(5):2920-32. PubMed
Winograd J, Reilly MP, Roe R, Lutz J, Laughner E, Xu X, Hu L, Asakura T, vander Kolk C, Strandberg JD, Semenza GL. Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. Hum Mol Genet. 1997 Mar;6(3):369-79. PubMed
Ros MA, Piedra ME, Fallon JF, Hurle JM. Morphogenetic potential of the chick leg interdigital mesoderm when diverted from the cell death program. Dev Dyn. 1997 Mar;208(3):406-19. PubMed
MacKenzie A, Purdie L, Davidson D, Collinson M, Hill RE. Two enhancer domains control early aspects of the complex expression pattern of Msx1. Mech Dev. 1997 Feb;62(1):29-40. PubMed
Ohuchi H, Shibusawa M, Nakagawa T, Ohata T, Yoshioka H, Hirai Y, Nohno T, Noji S, Kondo N. A chick wingless mutation causes abnormality in maintenance of Fgf8 expression in the wing apical ridge, resulting in loss of the dorsoventral boundary. Mech Dev. 1997 Feb;62(1):3-13. PubMed
Brown JM, Robertson KE, Wedden SE, Tickle C. Alterations in Msx 1 and Msx 2 expression correlate with inhibition of outgrowth of chick facial primordia induced by retinoic acid. Anat Embryol (Berl). 1997 Feb;195(2):203-7. PubMed
Iimura T, Takeda K, Goseki M, Maruoka Y, Sasaki S, Oida S. Characterization of two length cDNA for human MSX-2 from dental pulp-derived cells. DNA Seq. 1997;8(1-2):87-92. PubMed
Barlow AJ, Francis-West PH. Ectopic application of recombinant BMP-2 and BMP-4 can change patterning of developing chick facial primordia. Development. 1997 Jan;124(2):391-8. PubMed
Lidral AC, Murray JC, Buetow KH, Basart AM, Schearer H, Shiang R, Naval A, Layda E, Magee K, Magee W. Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. Cleft Palate Craniofac J. 1997 Jan;34(1):1-6. PubMed
Monsoro-Burq AH, Duprez D, Watanabe Y, Bontoux M, Vincent C, Brickell P, Le Douarin N. The role of bone morphogenetic proteins in vertebral development. Development. 1996 Nov;122(11):3607-16. PubMed
Ide SE, Ortiz de Luna RI, Francomano CA, Polymeropoulos MH. Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish. Hum Genet. 1996 Nov;98(5):572-5. PubMed
Iler N, Abate-Shen C. Rapid identification of homeodomain binding sites in the Wnt-5a gene using an immunoprecipitation strategy. Biochem Biophys Res Commun. 1996 Oct 3;227(1):257-65. PubMed
Chen Y, Bei M, Woo I, Satokata I, Maas R. Msx1 controls inductive signaling in mammalian tooth morphogenesis. Development. 1996 Oct;122(10):3035-44. PubMed
Chuong CM, Widelitz RB, Ting-Berreth S, Jiang TX. Early events during avian skin appendage regeneration
Phippard DJ, Weber-Hall SJ, Sharpe PT, Naylor MS, Jayatalake H, Maas R, Woo I, Roberts-Clark D, Francis-West PH, Liu YH, Maxson R, Hill RE, Dale TC. Regulation of Msx-1, Msx-2, Bmp-2 and Bmp-4 during foetal and postnatal mammary gland development. Development. 1996 Sep;122(9):2729-37. PubMed
Wang W, Chen X, Xu H, Lufkin T. Msx3
Gaan Y, Macias D, Duterque-Coquillaud M, Ros MA, Hurle JM. Role of TGF beta s and BMPs as signals controlling the position of the digits and the areas of interdigital cell death in the developing chick limb autopod. Development. 1996 Aug;122(8):2349-57. PubMed
Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet. 1996 Aug;13(4):417-21. PubMed
Thesleff I. Two genes for missing teeth. Nat Genet. 1996 Aug;13(4):379-80. PubMed
Friedmann Y, Daniel CW. Regulated expression of homeobox genes Msx-1 and Msx-2 in mouse mammary gland development suggests a role in hormone action and epithelial-stromal interactions. Dev Biol. 1996 Jul 10;177(1):347-55. PubMed
Simon HG, Oppenheimer S. Advanced mRNA differential display
Maas R, Chen YP, Bei M, Woo I, Satokata I. The role of Msx genes in mammalian development. Ann N Y Acad Sci. 1996 Jun 8;785:171-81. PubMed PMID: 8702124.
Watanabe Y, Le Douarin NM. A role for BMP-4 in the development of subcutaneous cartilage. Mech Dev. 1996 Jun;57(1):69-78. PubMed
Macias D, Gaan Y, Ros MA, Hurle JM. In vivo inhibition of programmed cell death by local administration of FGF-2 and FGF-4 in the interdigital areas of the embryonic chick leg bud. Anat Embryol (Berl). 1996 Jun;193(6):533-41. PubMed
Catron KM, Wang H, Hu G, Shen MM, Abate-Shen C. Comparison of MSX-1 and MSX-2 suggests a molecular basis for functional redundancy. Mech Dev. 1996 Apr;55(2):185-99. Erratum in
Kostakopoulou K, Vogel A, Brickell P, Tickle C. 'Regeneration' of wing bud stumps of chick embryos and reactivation of Msx-1 and Shh expression in response to FGF-4 and ridge signals. Mech Dev. 1996 Apr;55(2):119-31. PubMed PMID: 8861093.
Dealy CN, Kosher RA. IGF-I, insulin and FGFs induce outgrowth of the limb buds of amelic mutant chick embryos. Development. 1996 Apr;122(4):1323-30. PubMed
Zhang H, Catron KM, Abate-Shen C. A role for the Msx-1 homeodomain in transcriptional regulation
Lian JB, Stein GS, Stein JL, Van Wijnen A, McCabe L, Banerjee C, Hoffmann H. The osteocalcin gene promoter provides a molecular blueprint for regulatory mechanisms controlling bone tissue formation
Abud HE, Skinner JA, McDonald FJ, Bedford MT, Lonai P, Heath JK. Ectopic expression of Fgf-4 in chimeric mouse embryos induces the expression of early markers of limb development in the lateral ridge. Dev Genet. 1996;19(1):51-65. PubMed
Graw J. Genetic aspects of embryonic eye development in vertebrates. Dev Genet. 1996;18(3):181-97. Review. PubMed
Isaac VE, Patel L, Curran T, Abate-Shen C. Use of fluorescence resonance energy transfer to estimate intramolecular distances in the Msx-1 homeodomain. Biochemistry. 1995 Nov 21;34(46):15276-81. PubMed
Mastrobattista JM, Doll P, Blanton SH, Northrup H. Evaluation of candidate genes for familial brachydactyly. J Med Genet. 1995 Nov;32(11):851-4. PubMed
Satokata I, Uchiyama M. [Mice carrying null mutations of the homeotic genes Hoxa10 and Msx1]. Tanpakushitsu Kakusan Koso. 1995 Oct;40(14):2134-43. Review. Japanese. PubMed
Chen Y, Solursh M. Mirror-image duplication of the primary axis and heart in Xenopus embryos by the overexpression of Msx-1 gene. J Exp Zool. 1995 Oct 1;273(2):170-4. PubMed
Vogel A, Roberts-Clarke D, Niswander L. Effect of FGF on gene expression in chick limb bud cells in vivo and in vitro. Dev Biol. 1995 Oct;171(2):507-20. PubMed
Davidson D. The function and evolution of Msx genes
Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I. Gene defect in hypodontia
Woloshin P, Song K, Degnin C, Killary AM, Goldhamer DJ, Sassoon D, Thayer MJ. MSX1 inhibits myoD expression in fibroblast x 10T1/2 cell hybrids. Cell. 1995 Aug 25;82(4):611-20. PubMed
Chen Y, Kostetskii I, Zile MH, Solursh M. Comparative study of Msx-1 expression in early normal and vitamin A-deficient avian embryos. J Exp Zool. 1995 Jul 1;272(4):299-310. PubMed
Tureckov J, Sahlberg C, Aberg T, Ruch JV, Thesleff I, Peterkova R. Comparison of expression of the msx-1, msx-2, BMP-2 and BMP-4 genes in the mouse upper diastemal and molar tooth primordia. Int J Dev Biol. 1995 Jun;39(3):459-68. PubMed
Isaac VE, Sciavolino P, Abate C. Multiple amino acids determine the DNA binding specificity of the Msx-1 homeodomain. Biochemistry. 1995 May 30;34(21):7127-34. PubMed
Semenza GL, Wang GL, Kundu R. DNA binding and transcriptional properties of wild-type and mutant forms of the homeodomain protein Msx2. Biochem Biophys Res Commun. 1995 Apr 6;209(1):257-62. PubMed
Hollway GE, Phillips HA, Ads LC, Haan EA, Mulley JC. Localization of craniosynostosis Adelaide type to 4p16. Hum Mol Genet. 1995 Apr;4(4):681-3. PubMed
Reginelli AD, Wang YQ, Sassoon D, Muneoka K. Digit tip regeneration correlates with regions of Msx1 (Hox 7) expression in fetal and newborn mice. Development. 1995 Apr;121(4):1065-76. PubMed
Wang Y, Sassoon D. Ectoderm-mesenchyme and mesenchyme-mesenchyme interactions regulate Msx-1 expression and cellular differentiation in the murine limb bud. Dev Biol. 1995 Apr;168(2):374-82. PubMed
Crews L, Gates PB, Brown R, Joliot A, Foley C, Brockes JP, Gann AA. Expression and activity of the newt Msx-1 gene in relation to limb regeneration. Proc Biol Sci. 1995 Feb 22;259(1355):161-71. PubMed
Catron KM, Zhang H, Marshall SC, Inostroza JA, Wilson JM, Abate C. Transcriptional repression by Msx-1 does not require homeodomain DNA-binding sites. Mol Cell Biol. 1995 Feb;15(2):861-71. PubMed
Mina M, Gluhak J, Upholt WB, Kollar EJ, Rogers B. Experimental analysis of Msx-1 and Msx-2 gene expression during chick mandibular morphogenesis. Dev Dyn. 1995 Feb;202(2):195-214. PubMed
Iimura T, Oida S, Takeda K, Maruoka Y, Shimokawa H, Ibaraki K, Sasaki S. Molecular cloning and sequence of bovine Msx-1 homeobox-containing gene cDNA from a bovine odontoblast library. DNA Seq. 1995;5(4):233-7. PubMed
Weiss KM, Ruddle FH, Bollekens J. Dlx and other homeobox genes in the morphological development of the dentition. Connect Tissue Res. 1995;32(1-4):35-40. PubMed
Hoffmann HM, Catron KM, van Wijnen AJ, McCabe LR, Lian JB, Stein GS, Stein JL. Transcriptional control of the tissue-specific, developmentally regulated osteocalcin gene requires a binding motif for the Msx family of homeodomain proteins. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12887-91. PubMed PMID: 7809141; PubMed Central PMCID
Ferrari D, Kosher RA, Dealy CN. Limb mesenchymal cells inhibited from undergoing cartilage differentiation by a tumor promoting phorbol ester maintain expression of the homeobox-containing gene Msx1 and fail to exhibit gap junctional communication. Biochem Biophys Res Commun. 1994 Nov 30;205(1):429-34. PubMed
Ros MA, Lyons GE, Mackem S, Fallon JF. Recombinant limbs as a model to study homeobox gene regulation during limb development. Dev Biol. 1994 Nov;166(1):59-72. PubMed
Ros MA, Macias D, Fallon JF, Hurle JM. Formation of extra digits in the interdigital spaces of the chick leg bud is not preceded by changes in the expression of the Msx and Hoxd genes. Anat Embryol (Berl). 1994 Oct;190(4):375-82. PubMed
Bgue-Kirn C, Smith AJ, Loriot M, Kupferle C, Ruch JV, Lesot H. Comparative analysis of TGF beta s, BMPs, IGF1, msxs, fibronectin, osteonectin and bone sialoprotein gene expression during normal and in vitro-induced odontoblast differentiation. Int J Dev Biol. 1994 Sep;38(3):405-20. PubMed
Shang Z, Isaac VE, Li H, Patel L, Catron KM, Curran T, Montelione GT, Abate C. Design of a "minimAl" homeodomain
Robert B, Montagutelli X, Houzelstein D, Ferland L, Cohen A, Buckingham M, Gunet JL. Msx1 is close but not allelic to either Hm or Hx on mouse chromosome 5. Mamm Genome. 1994 Jul;5(7):446-9. PubMed
Stephenson DA, Lee KH, Nagle DL, Yen CH, Morrow A, Miller D, Chapman VM, Bućan M. Mouse rump-white mutation associated with an inversion of chromosome 5. Mamm Genome. 1994 Jun;5(6):342-8. PubMed
Wright EM. Cystinuria defect expresses itself. Nat Genet. 1994 Apr;6(4):328-9. PubMed
Satokata I, Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet. 1994 Apr;6(4):348-56. PubMed
Fallon JF, Lpez A, Ros MA, Savage MP, Olwin BB, Simandl BK. FGF-2
Rashbass P, Wilson V, Rosen B, Beddington RS. Alterations in gene expression during mesoderm formation and axial patterning in Brachyury (T) embryos. Int J Dev Biol. 1994 Mar;38(1):35-44. PubMed
Nishikawa K, Nakanishi T, Aoki C, Hattori T, Takahashi K, Taniguchi S. Differential expression of homeobox-containing genes Msx-1 and Msx-2 and homeoprotein Msx-2 expression during chick craniofacial development. Biochem Mol Biol Int. 1994 Mar;32(4):763-71. PubMed
Pavlova A, Boutin E, Cunha G, Sassoon D. Msx1 (Hox-7.1) in the adult mouse uterus
Shang Z, Ebright YW, Iler N, Pendergrast PS, Echelard Y, McMahon AP, Ebright RH, Abate C. DNA affinity cleaving analysis of homeodomain-DNA interaction: identification of homeodomain consensus sites in genomic DNA. Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):118-22. PubMed
Shen R, Chen Y, Huang L, Vitale E, Solursh M. Characterization of the human MSX-1 promoter and an enhancer responsible for retinoic acid induction. Cell Mol Biol Res. 1994;40(4):297-312. PubMed
Chan-Thomas PS, Thompson RP, Robert B, Yacoub MH, Barton PJ. Expression of homeobox genes Msx-1 (Hox-7) and Msx-2 (Hox-8) during cardiac development in the chick. Dev Dyn. 1993 Jul;197(3):203-16. PubMed
Catron KM, Iler N, Abate C. Nucleotides flanking a conserved TAAT core dictate the DNA binding specificity of three murine homeodomain proteins. Mol Cell Biol. 1993 Apr;13(4):2354-65. PubMed
Coelho CN, Upholt WB, Kosher RA. The expression pattern of the chicken homeobox-containing gene GHox-7 in developing polydactylous limb buds suggests its involvement in apical ectodermal ridge-directed outgrowth of limb mesoderm and in programmed cell death. Differentiation. 1993 Jan;52(2):129-37. PubMed
Hewitt JE, Clark LN, Ivens A, Williamson R. Structure and sequence of the human homeobox gene HOX7. Genomics. 1991 Nov;11(3):670-8. PubMed
Suzuki HR, Padanilam BJ, Vitale E, Ramirez F, Solursh M. Repeating developmental expression of G-Hox 7, a novel homeobox-containing gene in the chicken. Dev Biol. 1991 Nov;148(1):375-88. Erratum in

Home cDNA Library DeepCAGE Service Clone Distribution

Powered by Japan Bioinformatics K.K.