Prion protein PrPc interacts with molecular chaperones of the Hsp60 family.

Prions mediate the pathogenesis of certain neurodegenerative diseases, including bovine spongiform encephalopathy in cattle and Creutzfeldt-Jakob disease in humans. The prion particle consists mainly, if not entirely, of PrPSc, a posttranslationally modified isoform of the cellular host-encoded prio...

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Dades bibliogràfiques

Publicat a:	J Virol
Autors principals:	Edenhofer, F, Rieger, R, Famulok, M, Wendler, W, Weiss, S, Winnacker, E L
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Microbiology (ASM) 1996
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC190409/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8676499/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.70.7.4724-4728.1996
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