Common Structural Traits across Pathogenic Mutants of the Human Prion Protein and Their Implications for Familial Prion Diseases-Reference-Cited by-同舟云学术

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Common Structural Traits across Pathogenic Mutants of the Human Prion Protein and Their Implications for Familial Prion Diseases

Published:2011-08 Issue:3 Volume:411 Page:700-712
ISSN:0022-2836
Container-title:Journal of Molecular Biology
language:en
Short-container-title:Journal of Molecular Biology

Author:

Rossetti Giulia,Cong Xiaojing,Caliandro Rocco,Legname Giuseppe,Carloni Paolo

Funder

European Science Foundation

European Community's Seventh Framework Programme

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

Reference116 articles.

1. Prion diseases of humans and animals: their causes and molecular basis;Collinge;Annu. Rev. Neurosci.,2001

2. Prions;Prusiner;Proc. Natl Acad. Sci. USA,1998

3. Scrapie prion protein contains a phosphatidylinositol glycolipid;Stahl;Cell,1987

4. Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid;Stahl;Biochemistry,1992

5. Subcellular distribution and physicochemical properties of scrapie-associated precursor protein and relationship with scrapie agent;Safar;Neurology,1990

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