Regional heterogeneity of cellular prion protein isoforms in the mouse brain

Prion diseases are a group of invariably fatal neurodegenerative disorders that include Creutzfeldt–Jakob disease in humans, scrapie in sheep and goats, and bovine spongiform encephalopathy in cattle. The infectious agent or prion is largely composed of an abnormal isoform (PrPSc) of a host encoded...

Ful tanımlama

Detaylı Bibliyografya
Asıl Yazarlar: Beringue, V, Mallinson, G, Kaisar, M, Tayebi, M, Sattar, Z, Jackson, G, Anstee, D, Collinge, J, Hawke, S
Materyal Türü: Journal article
Dil:English
Baskı/Yayın Bilgisi: Oxford University Press 2003