Developmental impairments of craniofacial bone and cartilage in transgenic mice expressing FGF10

Mutations in a common extracellular domain of fibroblast growth factor receptor (FGFR)-2 isoforms (type IIIb and IIIc) cause craniosynostosis syndrome and chondrodysplasia syndrome. FGF10, a major ligand for FGFR2-IIIb and FGFR1-IIIb, is a key participant in the epithelial-mesenchymal interactions r...

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Detalles Bibliográficos
Autores principales: Yoshioka, Hirotaka, Kagawa, Kazuko, Minamizaki, Tomoko, Nakano, Masashi, Aubin, Jane E., Kozai, Katsuyuki, Tsuga, Kazuhiro, Yoshiko, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Full Length Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236464/
https://www.ncbi.nlm.nih.gov/pubmed/37275784
http://dx.doi.org/10.1016/j.bonr.2023.101692

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236464/
https://www.ncbi.nlm.nih.gov/pubmed/37275784
http://dx.doi.org/10.1016/j.bonr.2023.101692

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