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Ubiquitin-specific protease 14 modulates degradation of cellular prion protein

Prion diseases are fatal neurodegenerative disorders characterized by the accumulation of prion protein (PrP(C)). To date, there is no effective treatment for the disease. The accumulated PrP, termed PrP(Sc), forms amyloid fibrils and could be infectious. It has been suggested that PrP(Sc) is abnorm...

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Dades bibliogràfiques
Publicat a:Sci Rep
Autors principals: Homma, Takujiro, Ishibashi, Daisuke, Nakagaki, Takehiro, Fuse, Takayuki, Mori, Tsuyoshi, Satoh, Katsuya, Atarashi, Ryuichiro, Nishida, Noriyuki
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4462021/
https://ncbi.nlm.nih.gov/pubmed/26061634
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep11028
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