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Modeling human mutations to understand TRIO GEF function during development
DOI:10.1016/j.tins.2023.03.004.png)
摘要
En 中文
In a recent study, Bonnet and colleagues leveraged in silico structure prediction and human genetic data to understand the molecular regulation of the Rac1-activating guanie nucleotide exchange factor (Rac1-GEF) domain of Trio. Their work sheds new light on the role of Trio during axon guidance and explores the mechanism by which Trio GEF function is regulated in health and dysregulated in disease.
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期刊
IF:
15.1
论文数:
5.3K
被引数:
2.2W
机构
引用论文
Kalirin and Trio: RhoGEFs in Synaptic Transmission, Plasticity, and Complex Brain Disorders
TRENDS IN NEUROSCIENCES
IF15.1
An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio
NATURE COMMUNICATIONS
IF15.7
Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivo
MOLECULAR PSYCHIATRY
IF10.1
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