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The Function of Autophagy in Neurodegenerative DiseasesSignificance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonismCognitive dysfunction and depression in Parkinson's disease: what can be learned from rodent models?The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's diseasePINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients.Mechanisms, pathophysiological roles and methods for analyzing mitophagy - recent insights.Overexpression of Buffy enhances the loss of parkin and suppresses the loss of Pink1 phenotypes in Drosophila.Autophagy in Age-Associated Neurodegeneration.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
PARK6 is a common cause of familial parkinsonism.
@ast
PARK6 is a common cause of familial parkinsonism.
@en
PARK6 is a common cause of familial parkinsonism.
@nl
type
label
PARK6 is a common cause of familial parkinsonism.
@ast
PARK6 is a common cause of familial parkinsonism.
@en
PARK6 is a common cause of familial parkinsonism.
@nl
prefLabel
PARK6 is a common cause of familial parkinsonism.
@ast
PARK6 is a common cause of familial parkinsonism.
@en
PARK6 is a common cause of familial parkinsonism.
@nl
P2093
P50
P356
P1476
PARK6 is a common cause of familial parkinsonism.
@en
P2093
A Ferraris
A R Bentivoglio
B A Oostra
E A Graham
E M Valente
European Consortium on Genetic Susceptibility in Parkinson's Disease
F Brancati
G De Michele
P2888
P304
P356
10.1007/S100720200097
P478
23 Suppl 2
P577
2002-09-01T00:00:00Z