Analysis of the Fgfr2(C342Y) mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme

Syndromic craniosynostosis caused by mutations in FGFR2 is characterised by developmental pathology in both endochondral and membranous skeletogenesis. Detailed phenotypic characterisation of features in the membranous calvarium, the endochondral cranial base and other structures in the axial and ap...

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Detalles Bibliográficos
Autores principales: Peskett, Emma, Kumar, Samin, Baird, William, Jaiswal, Janhvi, Li, Ming, Patel, Priyanca, Britto, Jonathan A., Pauws, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312100/
https://www.ncbi.nlm.nih.gov/pubmed/28069589
http://dx.doi.org/10.1242/bio.022178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312100/
https://www.ncbi.nlm.nih.gov/pubmed/28069589
http://dx.doi.org/10.1242/bio.022178

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