PIN1 is a new therapeutic target of craniosynostosis

Gain-of-function mutations in fibroblast growth factor receptors (FGFRs) cause congenital skeletal anomalies, including craniosynostosis (CS), which is characterized by the premature closure of craniofacial sutures. Apert syndrome (AS) is one of the severest forms of CS, and the only treatment is su...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Shin, H R, Bae, H S, Kim, B S, Yoon, H I, Cho, Y D, Kim, W J, Choi, K Y, Lee, Y S, Woo, K M, Baek, J H, Ryoo, H M
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
General Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6216213/
https://ncbi.nlm.nih.gov/pubmed/30007339
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy252
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