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1)Tooze SA, Yoshimori T. The origin of the autophagosomal membrane. Nat Cell Biol. 2010; 12: 831-5
PubMed CrossRef
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2)Mizushima N, Komatsu M. Autophagy: reno-vation of cells and tissues. Cell. 2011; 147: 728-41
PubMed CrossRef
医中誌リンクサービス
3)Ravikumar B, Vacher C, Berger Z, et al. Inhi-bition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease. Nat Genet. 2004; 36: 585-95
PubMed CrossRef
医中誌リンクサービス
4)Bjørkøy G, Lamark T, Brech A, et al. p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death. J Cell Biol. 2005; 171: 603-14
PubMed CrossRef
医中誌リンクサービス
5)Hara T, Nakamura K, Matsui M, et al. Suppres-sion of basal autophagy in neural cells causes neurodegenerative disease in mice. Nature. 2006; 441: 885-9
PubMed
医中誌リンクサービス
6)Komatsu M, Waguri S, Chiba T, et al. Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature. 2006; 441: 880-4
PubMed
医中誌リンクサービス
7)Komatsu M, Waguri S, Koike M, et al. Homeo-static levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice. Cell. 2007; 131: 1149-63
PubMed CrossRef
医中誌リンクサービス
8)Pankiv S, Clausen TH, Lamark T, et al. p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy. J Biol Chem. 2007; 282: 24131-45
PubMed CrossRef
医中誌リンクサービス
9)Ichimura Y, Kumanomidou T, Sou Y-S, et al. Structural basis for sorting mechanism of p62 in selective autophagy. J Biol Chem. 2008; 283: 22847-57
PubMed CrossRef
医中誌リンクサービス
10)Van Der Veen AG, Ploegh HL. Ubiquitin-like proteins. Annu Rev Biochem. 2012; 81: 323-57
PubMed CrossRef
医中誌リンクサービス
11)Shaid S, Brandts CH, Serve H, et al. Ubiquiti-nation and selective autophagy. Cell Death Differ. 2012 Jun 22 [Epub ahead of print]
医中誌リンクサービス
12)Long J, Gallagher TRA, Cavey JR, et al. Ubiquitin recognition by the ubiquitin-associated domain of p62 involves a novel conformational switch. J Biol Chem. 2008; 283: 5427-40
PubMed
医中誌リンクサービス
13)Matsumoto G, Wada K, Okuno M, et al. Serine 403 phosphorylation of p62/SQSTM1 regulates selective autophagic clearance of ubiquitinated proteins. Mol Cell. 2011; 44: 279-89
PubMed CrossRef
医中誌リンクサービス
14)Filimonenko M, Isakson P, Finley KD, et al. The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy. Mol Cell. 2010; 38: 265-79
PubMed CrossRef
医中誌リンクサービス
15)Itakura E, Mizushima N. p62 Targeting to the autophagosome formation site requires self-oligomerization but not LC3 binding. J Cell Biol. 2011; 192: 17-27
PubMed CrossRef
医中誌リンクサービス
16)Mizushima N, Yamamoto A, Matsui M, et al. In vivo analysis of autophagy in response to nutrient starvation using transgenic mice expressing a fluorescent autophagosome marker. Mol Biol Cell. 2004; 15: 1101-11
PubMed
医中誌リンクサービス
17)Matsuda N, Sato S, Shiba K, et al. PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy. J Cell Biol. 2010; 189: 211-21
PubMed CrossRef
医中誌リンクサービス
18)Jin SM, Youle RJ. PINK1- and Parkin-mediated mitophagy at a glance. J Cell Sci. 2012; 125: 795-9
PubMed CrossRef
医中誌リンクサービス
19)Kondapalli C, Kazlauskaite A, Zhang N, et al. PINK1 is activated by mitochondrial membrane potential depolarization and stimulates Parkin E3 ligase activity by phosphorylating serine 65. Open Biol. 2012; 2: 120080
PubMed
医中誌リンクサービス
20)Woodroof HI, Pogson JH, Begley M, et al. Discovery of catalytically active orthologues of the Parkinsons disease kinase PINK1: analysis of substrate specificity and impact of mutations. Open Biol. 2011; 1: 110012
PubMed
医中誌リンクサービス
21)Behrends C, Sowa ME, Gygi SP, et al. Network organization of the human autophagy system. Nature. 2010; 466: 68-76
PubMed
医中誌リンクサービス
22)Lipinski MM, Zheng B, Lu T, et al. Genome-wide analysis reveals mechanisms modulating autophagy in normal brain aging and in Alzheimers disease. Proc Natl Acad Sci U S A. 2010; 107: 14164-9
PubMed CrossRef
医中誌リンクサービス
23)Zatloukal K, Stumptner C, Fuchsbichler A, et al. p62 is a common component of cytoplasmic inclusions in protein aggregation diseases. Am J Pathol. 2002; 160: 255-63
PubMed CrossRef
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