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Two Creutzfeldt–Jakob disease agents reproduce prion protein-independent identities in cell cultures

Human Creutzfeldt–Jakob disease (CJD) and similar neurodegenerative diseases such as sheep scrapie are caused by a variety of related infectious agents. They are associated with abnormal host prion protein (PrP), which is assessed by limited proteolysis to yield resistant PrP bands (PrP-res). Althou...

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Detalhes bibliográficos
Main Authors: Arjona, Alvaro, Simarro, Laura, Islinger, Florian, Nishida, Noriyuki, Manuelidis, Laura
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2004
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC423270/
https://ncbi.nlm.nih.gov/pubmed/15161970
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0400158101
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