标题
The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy
作者
关键词
-
出版物
CELL DEATH AND DIFFERENTIATION
Volume 17, Issue 6, Pages 962-974
出版商
Springer Nature
发表日期
2010-01-08
DOI
10.1038/cdd.2009.200
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Pink1 Forms a Multiprotein Complex with Miro and Milton, Linking Pink1 Function to Mitochondrial Trafficking†
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- Mendelian forms of Parkinson's disease
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- DAP-kinase-mediated phosphorylation on the BH3 domain of beclin 1 promotes dissociation of beclin 1 from Bcl-XL and induction of autophagy
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- Loss of Parkin or PINK1 Function Increases Drp1-dependent Mitochondrial Fragmentation
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- Discovery of Atg5/Atg7-independent alternative macroautophagy
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- Autophagy in neurodegeneration and development
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- Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
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- Characterization of PINK1 processing, stability, and subcellular localization
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- PINK1 Is Necessary for Long Term Survival and Mitochondrial Function in Human Dopaminergic Neurons
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- Cytoplasmic Pink1 activity protects neurons from dopaminergic neurotoxin MPTP
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- The kinase domain of mitochondrial PINK1 faces the cytoplasm
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- Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery
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