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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Society for Neuroscience 2013
Pynciau:
Articles
Mynediad Ar-lein: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
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