The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive.
Open Access
- 1 September 1991
- journal article
- abstracts
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 266 (27), 18217-18223
- https://doi.org/10.1016/s0021-9258(18)55257-1
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.The Journal of cell biology, 1990
- Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.The Journal of cell biology, 1990
- Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeExperimental Neurology, 1989
- Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeBiochemical and Biophysical Research Communications, 1989
- Scrapie and cellular PrP isoforms are encoded by the same chromosomal geneCell, 1986
- Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain TissueNew England Journal of Medicine, 1986
- Quantification of endocytosis-derived membrane trafficBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1985
- Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brainNature, 1985
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- Does the Agent of Scrapie Replicate without Nucleic Acid ?Nature, 1967