Gerstmann-Sträussler-Scheinker Disease and “Anchorless Prion Protein” Mice Share Prion Conformational Properties Diverging from Sporadic Creutzfeldt-Jakob Disease-Reference-Cited by-同舟云学术

Gerstmann-Sträussler-Scheinker Disease and “Anchorless Prion Protein” Mice Share Prion Conformational Properties Diverging from Sporadic Creutzfeldt-Jakob Disease

Published:2014-02 Issue:8 Volume:289 Page:4870-4881
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Zanusso Gianluigi,Fiorini Michele,Ferrari Sergio,Meade-White Kimberly,Barbieri Ilaria,Brocchi Emiliana,Ghetti Bernardino,Monaco Salvatore

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference30 articles.

1. Prions;Prusiner;Proc. Natl. Acad. Sci. U.S.A,1998

2. Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions;Caughey;Annu. Rev. Biochem,2009

3. Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein;Stahl;Biochemistry,1990

4. Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C;Stahl;Biochemistry,1990

5. Truncated forms of the human prion protein in normal brain and in prion diseases;Chen;J. Biol. Chem,1995

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