Septal chondrocyte hypertrophy contributes to midface deformity in a mouse model of Apert syndrome

Midface hypoplasia is a major manifestation of Apert syndrome. However, the tissue component responsible for midface hypoplasia has not been elucidated. We studied mice with a chondrocyte-specific Fgfr2(S252W) mutation (Col2a1-cre; Fgfr2(S252W/+)) to investigate the effect of cartilaginous component...

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Detalles Bibliográficos
Autores principales: Kim, Bong-Soo, Shin, Hye-Rim, Kim, Hyun-Jung, Yoon, Heein, Cho, Young-Dan, Choi, Kang-Young, Choi, Je-Yong, Kim, Woo-Jin, Ryoo, Hyun-Mo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041873/
https://www.ncbi.nlm.nih.gov/pubmed/33846505
http://dx.doi.org/10.1038/s41598-021-87260-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041873/
https://www.ncbi.nlm.nih.gov/pubmed/33846505
http://dx.doi.org/10.1038/s41598-021-87260-5

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