UBE3A公司
安吉曼综合征
生物
弧(几何)
泛素连接酶
AMPA受体
遗传学
神经发育障碍
神经科学
泛素
基因
NMDA受体
受体
几何学
数学
作者
Hwan‐Ching Tai,Beatriz Alvarez‐Castelao
出处
期刊:Cell
[Elsevier]
日期:2010-03-01
卷期号:140 (5): 608-610
被引量:7
标识
DOI:10.1016/j.cell.2010.02.019
摘要
Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited UBE3A gene, which encodes a ubiquitin ligase. Greer et al. (2010) now identify a UBE3A substrate called Arc that promotes endocytosis of neuronal AMPA receptors, providing insight into synaptic defects that may underlie the cognitive deficits in Angelman syndrome.
科研通智能强力驱动
Strongly Powered by AbleSci AI