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Misfolded PrP and a novel mechanism of proteasome inhibition

Prion diseases comprise a family of fatal neurodegenerative disorders caused by the conformational re-arrangement of a normal host-encoded protein, PrP(C), to an abnormal infectious isoform termed PrP(Sc). Currently, the precise cellular mechanism(s) underlying prion disease pathogenesis remain uncl...

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Detalhes bibliográficos
Main Authors: Andre, Ralph, Tabrizi, Sarah J
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3338962/
https://ncbi.nlm.nih.gov/pubmed/22453175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.6.1.18272
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