Msx homeobox gene family and craniofacial development

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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

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Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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Signalling networks regulating dental development

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A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene

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MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

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The signalling molecule BMP4 mediates apoptosis in the rhombencephalic neural crest

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STUDY OF SUTURAL MORPHOLOGY OF PTERION AMONG HUMAN ADULT NEPALESE SKULLS

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Cleft lip and palate: Associated genetic and environmental factorsImmunodeficiency Virus

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How the diversity of the faces arises

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Tooth Morphogenesis and Patterning: Molecular Genetics

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Gene Discovery in Nonsyndromic Cleft Lip with or without Cleft Palate

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DVL1 variants and C-terminal deletions have differential effects on craniofacial development and WNT signalingPreprint

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Association of rs8670 Polymorphism in the MSX1 Gene With Non-Syndromic Cleft Lip With or Without Cleft Palate in Malay Population

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Identification of Novel and Rare Gene Variants in Cleft Lip/Palate Patients From Kuwaiti Consanguineous Families by Exome Sequencing

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New Insights About Early Tongue Teeth Development in the Salmon Trout ( Oncorhynchus mykiss )

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Mutation of murine Sox4 untranslated regions results in partially penetrant perinatal lethality.

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Expression of interferon regulatory factor 6, muscle segment homeobox 1, paired box gene 9, homeo box B3, and related to tyrosine kinases in human cleft-affected tissue

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Generation of a MSX1 knockout human embryonic stem cell line using CRISPR/Cas9 technology

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Craniofacial Development and Disorders—Contributions of Xenopus

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Historic Background and Current Perspectives in Dental Crown Formation

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Effect of Deferoxamine on Rat Fetal Bone Formation and on it is Certain Regulating Genes

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Genes and Gene Networks Regulating Mineralization

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The minimum free energy of G-quadruplex-forming sequences of the MSX1 intron is associated with relative molar and premolar size in eutherians

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Insights into Suture Stem Cells: Distributions, Characteristics, and Applications

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Single‐Cell Analysis of Alternative Splicing and Gene Regulatory Network Reveals Remarkable Expression and Regulation Dynamics During Human Early Embryonic Development

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Homeobox family Hoxc localization during murine palate formation

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Dental Development and Anomalies in Cleft Lip and Palate

Tan, E. L. Y., & Yow, M. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.88310 · Cited by 1

Implications of specific gene expression patterns in enamel knot in tooth development

Kim, T.-Y., Neupane, S., Aryal, Y. P., Lee, E.-S., Kim, J., Suh, J., Lee, Y., Sohn, W., An, S., Ha, J., et al. (2020) · International Journal of Oral Biology · doi:10.11620/ijob.2020.45.1.25 · Cited by 1

Temporo-spatial distribution of stem cell markers CD146 and p75NTR during odontogenesis in mice

de Queiroz, A. C., Pelissari, C., Arana-Chavez, V. E., & Martins, M. T. (2021) · Journal of Applied Oral Science · doi:10.1590/1678-7757-2021-0138 · Cited by 1

FGFR and inhibitors

Li, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15793-6.00008-1 · Cited by 1

Definitions, Prevalence and Aetiology

Hobkirk, J. A., Gill, D. S., Jones, S. P., Hemmings, K. W., Bassi, G. S., O'Donnell, A. L., & Goodman, J. R. (2010) · Wiley eBooks · doi:10.1002/9781118784877.ch1 · Cited by 1

Nasal Cavity and Sinuses

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Investigação de fatores genéticos na etiologia de fendas orofaciais típicas

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Analyse von Wechselwirkungen der Homeodomäninteragierenden Proteinkinase (Hipk) in Drosophila melanogaster unter besonderer Berücksichtigung des Interaktionspartners Spenito (Nito)

Dewald, D. N. (2014) · Publications of the UdS (Saarland University) · doi:10.22028/d291-21841

Utilização da técnica de Open Array para investigação de genes associados a fendas labiopalatais em amostra da população brasileira

de Araujo, T. K. (2015) · doi:10.47749/t/unicamp.2015.946252

Determination of the role and regulation of matrix metalloproteinase-25 during mouse secondary palate formation

Brown, G. D. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)

Estudo das alterações na expressão gênica dos ependimomas

de Andrade, F. G. (2014) · doi:10.11606/t.5.2014.tde-01092014-154140

Epigenetic Modifications in Testicular Germ Cell Tumors

Payne, C. (2012) · InTech eBooks · doi:10.5772/33483

Gene expression analysis of Flrt1, Flrt2 and Flrt3 in the murine midface during early embryogenesis

Chung, K. C. (2009) · TSpace (University of Toronto)

The role of Hoxa2 and characterization of its new downstream targets in murine palatogenesis

Smith, T. M. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)

Comparative Developmental Transcriptomics of Echinoderms

Vaughn, R. (2012) · Digital Commons - University of South Florida (University of South Florida)

MSX1 in relation to clefting. hypodontia and hydrocephaly in humans

van den Boogaard, M. H. (2013) · Utrecht University Repository (Utrecht University)

Study of three non‐syndromic cases of congenital thumb aplasia in captive rhesus monkeys

Goldschmidt, B., Meireles, B. C. D. S., Calado, M. I. Z., França, F. G. O., de Oliveira, A. G. L., & Resende, F. C. (2015) · Journal of Medical Primatology · doi:10.1111/jmp.12175

Ectodermal organ development: Regulation by Notch and Eda pathways

Mustonen, T. (2004) · Työväentutkimus Vuosikirja

Uma Busca pelas causas genéticas de agenesias dentárias não sindrômicas

Braga, T. (2009) · Lume (Universidade Federal do Rio Grande do Sul)

Unravelling the induction and development of intramembranous bones in the chicken eye

Duench, K. (2010) · Saint Mary's University Institutional Repository (Saint Mary's University)

Analise de polimorfismos na região de intro do gene MSX1 em individuos com hipodontia

Saito, C. P. B. (2005) · doi:10.47749/t/unicamp.2005.339186

Associação dos polimorfismos nos genes HOXD1, TNP1, MSX1, TCOF1, FGFR1, COL2A1, WNT3 e TIMP3 com fissuras de lábio e/ou palato não-sindrômica em uma população brasileira

Machado, R. A. (2015) · doi:10.47749/t/unicamp.2015.946399

Investigação clínica e genética de uma família brasileira com aniridia congênita

Fernandes-Lima, Z. S. (2014) · Americanae (AECID Library)

Hedgehog Signaling in Palatal and Facial Development

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A Review of Orofacial Clefting and Current Genetic Mouse Models

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Estudo de associação entre polimorfismo genético e os fenótipos fissura labiopalatina e agenesia dentária não sindrômicas

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The role of mechanical force and the Eda pathway on morphogenesis of molar roots

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Changing the face of craniosynostosis: the role of RBP4 in osteogenesis and suture fusion.

Leitch, V. D. (2011) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

Role of Hoxa2 and its Putative Downstream Target Htra1 in Osteogenic Differentiation of the Palatal Mesenchyme

Iyyanar, P. P. R. (2018) · HARVEST (University of Saskatchewan)

Neural crest cells: Evolution, embryonic bases and craniofacial development. Systematic literature review

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Variations in the Number of Teeth

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Odontological analysis of Polish children with unilateral cleft lip and palate

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Drosophila Homeodomain-Interacting Protein Kinase (Hipk) Phosphorylates the Homeodomain Proteins Homeobrain, Empty Spiracles, and Muscle Segment Homeobox

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Oral biosciences: The annual review 2019

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Estudo de regiões evolutivamente conservadas e de fatores de transcrição possivelmente envolvidos na regulação da expressão do gene da 'Miostatina' em vertebrados

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The absence of muscle segment homeobox 2 leads to the pyroptosis of ameloblasts by inducing squamous epithelial hyperplasia in the enamel organ

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A Novel Cyclic Acetal Biomaterial and Its Use in Cleft Palate Repair

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Faculty Opinions recommendation of Insights into the genetic architecture of the human face.

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Embryology Update

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Síndrome de Goldenhar. Reporte de un caso

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Investigation of Genes and Gene Proteins in Cleft Affected Tissue. Summary of the Doctoral Thesis

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Gēnu un gēnu proteīnu izpēte dažādu šķeltņu skartos audos. Promocijas darba kopsavilkums

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Gēnu un gēnu proteīnu izpēte dažādu šķeltņu skartos audos. Promocijas darbs

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Altered chromatin landscape and 3D interactions associated with primary constitutional MLH1 epimutations

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Current insights on the genetics and mechanisms of MSX1-associated cleft palate

Myo, A. C., Raju, R., Piña, J. O., Chattaraj, P., & Furukawa, M. (2025) · Frontiers in Dental Medicine · doi:10.3389/fdmed.2025.1610223

Identification of two novel variants in homeodomain of MSX1 associated with oligodontia

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Impact of substrate choice on human osteoclast differentiation and secretome: Implications for targeted therapeutic development

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Additional file 1 of Family and case–control genetic study of MSX1 polymorphisms in peg-shaped teeth Jordanian population

Alkhatib, R., Hawamdeh, R., AL-Eitan, L. N., Abdo, N., Obeidat, F., Al-Bataineh, M. M., & Aman, H. (2022) · Figshare · doi:10.6084/m9.figshare.18866652

Additional file 2 of Family and case–control genetic study of MSX1 polymorphisms in peg-shaped teeth Jordanian population

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Genome Evolution and the Enigmatic Axial Skeleton of the Hero Shrew (Soricidae: Scutisorex Somereni )

Chipps, A. S., Hutter, C. R., Demos, T. C., & Esselstyn, J. A. (2026) · Genome Biology and Evolution · doi:10.1093/gbe/evag048

Rôle des cellules orales dérivées des crêtes neurales dans la morphogenèse craniofaciale

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Msx2 et Sost/Sclérostine : deux modulateurs du développement et de la réparation de la dentine

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The Role of SHH Signaling in Regulating Species-Specific Jaw Size

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Loss of p130Cas/Bcar1 impairs palatal mesenchymal expansion and causes cleft palate

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Craniofacial development: genetics, signaling pathways, teratogenic mechanisms, and clinal significance

Lv, X., & Du, J. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00574-6

Effect of Homeobox Gene Msx in Craniomaxillofacial Development

Xian-xian, Y. (2005) · Acta Universitatis Medicinalis Secondae Shanghai

Msx1 et son influence sur la croissance cranio-faciale

Vi‐Fane, B., Fernandes, I., & Davideau, J. (2007) · L Orthodontie Française · doi:10.1051/orthodfr:2007007 · Cited by 8

THE EXPRESSION OF MSX GENES DURING EARLY CRANIAL SUTURE EMBRYOGENESIS

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Activity of msx-1 type genes during craniofacial development

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The function and evolution of Msx genes: pointers and paradoxes

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