Redox mechanisms and their pathological role in prion diseases: The road to ruin.

Prion diseases, also known as transmissible spongiform encephalopathies, are rare, progressive, and fatal neurodegenerative disorders, which are caused by the accumulation of the misfolded cellular prion protein (PrPC). The resulting cytotoxic prion species, referred to as the scrapie prion isoform...

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Bibliographic Details
Main Authors: Jereme G Spiers, Hsiao-Jou Cortina Chen, Joern R Steinert
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-04-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1011309