Insoluble wild–type and protease–resistant mutant prion protein in brains of patients with inherited prion disease-Reference-Cited by-同舟云学术

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Insoluble wild–type and protease–resistant mutant prion protein in brains of patients with inherited prion disease

Published:1996-01 Issue:1 Volume:2 Page:59-64
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Gabizon Ruth,Telling Glenn,Meiner Zeev,Halimi Michele,Kahana Irit,Prusiner Stanley B.

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm0196-59.pdf

Reference47 articles.

1. Prusiner, S.B. Inherited prion diseases. Proc. Natl. Acad. Sci. USA 91, 4611–4614 (1994).

2. Masters, C.L., Gajdusek, D.C. & Gibbs, C.J., Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Straussler syndrome. Brain 1O4, 559–588 (1981).

3. Hsiao, K. et al. Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome. Nature 338, 342–345 (1989).

4. Goldfarb, L.G. et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism. Science 258, 806–808 (1992).

5. Kahana, E., Milton, A., Braham, J. & Sofer, D. Creutzfeldt–Jakob disease: Focus among Libyan Jews in Israel. Science 183, 90–91 (1974).

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