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Increased expression of p62/SQSTM1 in prion diseases and its association with pathogenic prion protein

Prion diseases are neurodegenerative disorders characterized by the aggregation of abnormally folded prion protein (PrP(Sc)). In this study, we focused on the mechanism of clearance of PrP(Sc), which remains unclear. p62 is a cytosolic protein known to mediate both the formation and degradation of a...

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מידע ביבליוגרפי
Main Authors: Homma, Takujiro, Ishibashi, Daisuke, Nakagaki, Takehiro, Satoh, Katsuya, Sano, Kazunori, Atarashi, Ryuichiro, Nishida, Noriyuki
פורמט: Artigo
שפה:Inglês
יצא לאור: Nature Publishing Group 2014
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3968452/
https://ncbi.nlm.nih.gov/pubmed/24675871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep04504
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