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Oligomerization of Lrrk controls actin severing and α-synuclein neurotoxicity in vivo

BACKGROUND: Mutations in LRRK2 are the most common cause of familial Parkinson’s disease and typically cause disease in the context of abnormal aggregation and deposition of α-synuclein within affected brain tissue. METHODS: We combine genetic analysis of Lrrk-associated toxicity in a penetrant Dros...

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Detalhes bibliográficos
Publicado no:Mol Neurodegener
Main Authors: Sarkar, Souvarish, Bardai, Farah, Olsen, Abby L., Lohr, Kelly M., Zhang, Ying-Yi, Feany, Mel B.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8142648/
https://ncbi.nlm.nih.gov/pubmed/34030727
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13024-021-00454-3
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