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Correlation of Cellular Factors and Differential Scrapie Prion Permissiveness in Ovine Microglia

Prion diseases are fatal neurodegenerative disorders by which the native cellular prion protein (PrP(C)) is misfolded into an accumulating, disease-associated isoform (PrP(D)). To improve the understanding of prion pathogenesis and develop effective treatments, it is essential to elucidate factors c...

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Bibliografski detalji
Izdano u:Virus Res
Glavni autori: Dinkel, Kelcey D., Schneider, David A., Muñoz-Gutiérrez, Juan F., McElliott, Valerie R., Stanton, James B.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5771472/
https://ncbi.nlm.nih.gov/pubmed/28754560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.virusres.2017.07.016
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