Subclinical prion infection in humans and animals

Author:

Hill Andrew F,Collinge John

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference38 articles.

1. Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science1982; 216: 136–44

2. Büeler H, Aguzzi A, Sailer A et al. Mice devoid of PrP are resistant to scrapie. Cell1993; 73: 1339–47

3. Bruce ME, Fraser H, McBride PA, Scott JR, Dickinson AG. The basis of strain variation in scrapie. In: Prusiner SB, Collinge J, Powell J, Anderton B. (eds) Prion Diseases in Human and Animals. London: Ellis Horwood, 1992: 497–508

4. Bruce M, Chree A, McConnell I, Foster J, Pearson G, Fraser H. Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier. Philos Trans R Soc Lond B Biol Sci1994; 343: 405–11

5. Bessen RA, Marsh RF. Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent. J Virol1992; 66: 2096–101

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