Correlation of cellular factors and differential scrapie prion permissiveness in ovine microglia.
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DOI: 10.1016/j.virusres.2017.07.016
Abstract: Prion diseases are fatal neurodegenerative disorders by which the native cellular prion protein (PrPC) is misfolded into an accumulating, disease-associated isoform (PrPD). To improve the understanding of prion pathogenesis and develop effective treatments, it is… read more here.
Keywords: prion; permissiveness; cellular factors; correlation cellular ... See more keywords