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Synphilin-1 attenuates mutant LRRK2-induced neurodegeneration in Parkinson's disease models

Mutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal-dominant Parkinsonism with pleomorphic pathology including deposits of aggregated protein and neuronal degeneration. The pathogenesis of LRRK2-linked Parkinson's disease (PD) is not fully understood. Here, using co-immunoprecipit...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Liu, Jingnan, Li, Tianxia, Thomas, Joseph M., Pei, Zhong, Jiang, Haibing, Engelender, Simone, Ross, Christopher A., Smith, Wanli W.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4743687/
https://ncbi.nlm.nih.gov/pubmed/26744328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv504
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