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Overexpression of Parkin Ameliorates Dopaminergic Neurodegeneration Induced by 1- Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine in Mice

Mutations in the parkin gene are currently thought to be the most common cause of recessive familial Parkinsonism. Parkin functions as an E3 ligase to regulate protein turnover, and its function in mitochondrial quality control has been reported recently. Overexpression of parkin has been found to p...

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Detalhes bibliográficos
Main Authors: Bian, Minjuan, Liu, Jie, Hong, Xiaoqi, Yu, Mei, Huang, Yufang, Sheng, Zhejin, Fei, Jian, Huang, Fang
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3390003/
https://ncbi.nlm.nih.gov/pubmed/22792139
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0039953
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