Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Homma, Takujiro, Ishibashi, Daisuke, Nakagaki, Takehiro, Satoh, Katsuya, Sano, Kazunori, Atarashi, Ryuichiro, Nishida, Noriyuki
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2014
Matèries:
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!