Glycosylation Deficiency at Either One of the Two Glycan Attachment Sites of Cellular Prion Protein Preserves Susceptibility to Bovine Spongiform Encephalopathy and Scrapie Infections-Reference-Cited by-同舟云学术

Glycosylation Deficiency at Either One of the Two Glycan Attachment Sites of Cellular Prion Protein Preserves Susceptibility to Bovine Spongiform Encephalopathy and Scrapie Infections

Published:2004-12 Issue:51 Volume:279 Page:53306-53316
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Neuendorf Erdmute,Weber Artur,Saalmueller Armin,Schatzl Hermann,Reifenberg Kurt,Pfaff Eberhardt,Groschup Martin Hermann

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference68 articles.

1. Identification of a Protein That Purifies with the Scrapie Prion

2. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

3. A cellular gene encodes scrapie PrP 27-30 protein

4. Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.

5. Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing

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