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Rapid formation of amyloid from α-monomeric recombinant human PrP in vitro

The infectious agent of prion diseases is identified with PrP(Sc), a β-rich, amyloidogenic and partially protease resistant isoform of the cellular glycoprotein, PrP(C). To understand the process of prion formation in vivo, we and others have studied defined misfolding pathways of recombinant PrP in...

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Библиографические подробности
Главные авторы: Tahiri-Alaoui, Abdessamad, James, William
Формат: Artigo
Язык:Inglês
Опубликовано: Cold Spring Harbor Laboratory Press 2005
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2253435/
https://ncbi.nlm.nih.gov/pubmed/15741327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1110/ps.041000905
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