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Prion formation, but not clearance, is supported by protein misfolding cyclic amplification

Prion diseases are fatal transmissible neurodegenerative disorders that affect animals including humans. The kinetics of prion infectivity and PrP(Sc) accumulation can differ between prion strains and within a single strain in different tissues. The net accumulation of PrP(Sc) in animals is controll...

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Pubblicato in:Prion
Autori principali: Shikiya, Ronald A, Eckland, Thomas E, Young, Alan J, Bartz, Jason C
Natura: Artigo
Lingua:Inglês
Pubblicazione: Taylor & Francis 2014
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4601219/
https://ncbi.nlm.nih.gov/pubmed/25482601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/19336896.2014.983759
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