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Acute cellular uptake of abnormal prion protein is cell type and scrapie strain independent

Transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases that include Creutzfeldt-Jakob disease, bovine spongiform encephalopathy and sheep scrapie. Although one of the earliest events during TSE infection is the cellular uptake of protease resistant prion protein (PrP-r...

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Autors principals: Greil, Christopher S., Vorberg, Ina M., Ward, Anne E., Meade-White, Kimberly D., Harris, David A., Priola, Suzette A.
Format: Artigo
Idioma:Inglês
Publicat: 2008
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2614895/
https://ncbi.nlm.nih.gov/pubmed/18692214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.virol.2008.07.006
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