PrP(TSE) Distribution in a Primate Model of Variant, Sporadic, and Iatrogenic Creutzfeldt-Jakob Disease

Human prion diseases, such as Creutzfeldt-Jakob disease (CJD), are neurodegenerative and fatal. Sporadic CJD (sCJD) can be transmitted between humans through medical procedures involving highly infected organs, such as the central nervous system. However, in variant CJD (vCJD), which is due to human...

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Detalhes bibliográficos
Main Authors: Herzog, Christian, Rivière, Julie, Lescoutra-Etchegaray, Nathalie, Charbonnier, Aurore, Leblanc, Virginie, Salès, Nicole, Deslys, Jean-Philippe, Lasmézas, Corinne Ida
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology 2005
Assuntos:
Pathogenesis and Immunity
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1280201/
https://ncbi.nlm.nih.gov/pubmed/16254368
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.79.22.14339-14345.2005
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