A carregar...

Loss of Ahi1 Affects Early Development by Impairing BM88/Cend1-Mediated Neuronal Differentiation

Mutations in the Abelson helper integration site-1 (AHI1) gene result in N-terminal Ahi1 fragments and cause Joubert syndrome, an autosomal recessive brain malformation disorder associated with delayed development. How AHI1 mutations lead to delayed development remains unclear. Here we report that f...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Weng, Ling, Lin, Yung-Feng, Li, Alina L., Wang, Chuan-En, Yan, Sen, Sun, Miao, Gaertig, Marta A., Mitha, Naureen, Kosaka, Jun, Wakabayashi, Taketoshi, Xu, Xingshun, Tang, Beisha, Li, Shihua, Li, Xiao-Jiang
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3703472/
https://ncbi.nlm.nih.gov/pubmed/23658157
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0119-13.2013
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!