| Literature DB >> 23479001 |
Abstract
Prion diseases are a class of fatal neurodegenerative disorders that can be sporadic, genetic or iatrogenic. They are characterized by the unique nature of their etiologic agent: prions (PrP(Sc)). A prion is an infectious protein with the ability to convert the host-encoded cellular prion protein (PrP(C)) into new prion molecules by acting as a template. Since Stanley B. Prusiner proposed the "protein-only" hypothesis for the first time, considerable effort has been put into defining the role played by PrP(C) in neurons. However, its physiological function remains unclear. This review summarizes the major findings that support the involvement of PrP(C) in signal transduction.Entities:
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Year: 2013 PMID: 23479001 PMCID: PMC6275729 DOI: 10.2478/s11658-013-0085-0
Source DB: PubMed Journal: Cell Mol Biol Lett ISSN: 1425-8153 Impact factor: 5.787