Complementary hydropathy identifies a cellular prion protein receptor-Reference-Cited by-同舟云学术

Complementary hydropathy identifies a cellular prion protein receptor

Published:1997-12 Issue:12 Volume:3 Page:1376-1382
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Martins Vilma R.,Graner Edgard,Garcia-Abreu José,De Souza Sandro J.,Mercadante Adriana F.,Veiga Silvio S.,Zanata Silvio M.,Neto Vivaldo Moura,Brentani Ricardo R.

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm1297-1376.pdf

Reference32 articles.

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2. Prusiner, S.B. Molecular biology of prion diseases. Science 252, 1515–1522 (1991).

3. Weissman, C. Molecular biology of prion diseases. Trends Cell Biol. 4, 10–14 (1994).

4. Baster, K. et al. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell 46, 417–428 (1986).

5. Pan, K.-M. et al. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. Proc. Natl. Acad. Sci. USA 90, 10962–10966 (1993).

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