Dopamine neuron-specific LRRK2 G2019S effects on gene expression revealed by translatome profiling

Leucine-rich repeat kinase 2 (LRRK2) mutations are the most common genetic cause of late-onset Parkinson's disease. The pathogenic G2019S mutation enhances LRRK2 kinase activity and induces neurodegeneration in C. elegans, Drosophila and rodent models through unclear mechanisms. Gene expression...

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Bibliographic Details
Main Authors: Judit Pallos, Sophia Jeng, Shannon McWeeney, Ian Martin
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S096999612100139X