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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Lenguaje:Inglês
Publicado: Society for Neuroscience 2013
Materias:
Articles
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares