Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein-Reference-Cited by-同舟云学术

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

Published:1995-02-01 Issue:2 Volume:9 Page:197-201
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Whittington Miles A.,Sidle Katie C.L.,Gowland Ian,Meads Julie,Hill Andrew F.,Palmer Mark S.,Jefferys John G.R.,Collinge John

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0295-197.pdf

Reference33 articles.

1. Weller, R.O. latrogenic transmission of Creutzfeldt-Jakob disease. Psychol. Med. 19, 1–4 (1989).

2. Prusiner, S.B., Biology of Priori Diseases. Science 252, 1515–1522 (1991).

3. Borchelt, D.R., Scott, M., Taraboulos, A., Stahl, N. & Prusiner, S.B. Scraple and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells. J Cell Biol. 110, 743–752 (1990).

4. Gasset, M., Baldwin, M.A., Fletterick, R.J. & Prusiner, S.B. Perturbation of the secondary structure of the scrapie prion protein under conditions that alter Infectivity. Proc. natn. Acad. Sci. U.S.A. 90, 1–5 (1993).

5. Pan, K. et al. Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins. Proc natn. Acad Sci U.S.A., 90, 10962–10966 (1993).

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