Misfolding of the Prion Protein at the Plasma Membrane Induces Endocytosis, Intracellular Retention and Degradation
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1398-9219.2004.00185.x/fullpdf
Reference47 articles.
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3. The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive;Caughey;J Biol Chem,1991
4. Site-specific characterization of the N-linked glycans of murine prion protein by high-performance liquid chromatography/electrospray mass spectrometry and exoglycosidase digestions;Stimson;Biochemistry,1999
5. Glycosylation differences between the normal and pathogenic prion protein isoforms;Rudd;Proc Natl Acad Sci U S A,1999
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