Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R )mice

BACKGROUND: Apert syndrome is characterized by craniosynostosis and limb abnormalities and is primarily caused by FGFR2 +/P253R and +/S252W mutations. The former mutation is present in approximately one third whereas the latter mutation is present in two-thirds of the patients with this condition. W...

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Detalles Bibliográficos
Autores principales: Wang, Yingli, Sun, Miao, Uhlhorn, Victoria L, Zhou, Xueyan, Peter, Inga, Martinez-Abadias, Neus, Hill, Cheryl A, Percival, Christopher J, Richtsmeier, Joan T, Huso, David L, Jabs, Ethylin Wang
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838826/
https://www.ncbi.nlm.nih.gov/pubmed/20175913
http://dx.doi.org/10.1186/1471-213X-10-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838826/
https://www.ncbi.nlm.nih.gov/pubmed/20175913
http://dx.doi.org/10.1186/1471-213X-10-22

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