Nalaganje...
Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse
FGFR2c regulates many aspects of craniofacial and skeletal development. Mutations in the FGFR2 gene are causative of multiple forms of syndromic craniosynostosis, including Crouzon syndrome. Paradoxically, mouse studies have shown that the activation (Fgfr2c(C342Y); a mouse model for human Crouzon s...
Shranjeno v:
| izdano v: | Dis Model Mech |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Company of Biologists Ltd
2018
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6262810/ https://ncbi.nlm.nih.gov/pubmed/30266836 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.035311 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|