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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Edenhofer, F, Rieger, R, Famulok, M, Wendler, W, Weiss, S, Winnacker, E L
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1996
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC190409/
https://ncbi.nlm.nih.gov/pubmed/8676499
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