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Genome-wide RNAi screen identifies the Parkinson disease GWAS risk locus SREBF1 as a regulator of mitophagy

Genetic analysis of Parkinson disease (PD) has identified several genes whose mutation causes inherited parkinsonism, as well as risk loci for sporadic PD. PTEN-induced kinase 1 (PINK1) and parkin, linked to autosomal recessive PD, act in a common genetic pathway regulating the autophagic degradatio...

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書誌詳細
主要な著者: Ivatt, Rachael M., Sanchez-Martinez, Alvaro, Godena, Vinay K., Brown, Stephen, Ziviani, Elena, Whitworth, Alexander J.
フォーマット: Artigo
言語:Inglês
出版事項: National Academy of Sciences 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4060696/
https://ncbi.nlm.nih.gov/pubmed/24912190
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1321207111
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