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Molecular and Cellular Biology|September 21, 2001
Induction of distinct [URE3] yeast prion strainsM Schlumpberger, S B Prusiner, I Herskowitz
Ciba Foundation Symposium|January 1, 1988
Properties of scrapie prion proteins in liposomes and amyloid rodsR Gabizon, M P McKinley, S B Prusiner
The EMBO Journal|December 2, 1996
Chemical chaperones interfere with the formation of scrapie prion proteinJ Tatzelt, S B Prusiner, W J Welch
Journal of Neurochemistry|October 1, 1981
Culture and characterization of epithelial cells from bovine choroid plexusR B Crook, H Kasagami, S B Prusiner
Trends in Neurosciences|June 1, 1989
Unraveling prion diseases through molecular geneticsD Westaway, G A Carlson, S B Prusiner
The Journal of Biological Chemistry|August 15, 1992
Evidence for synthesis of scrapie prion proteins in the endocytic pathwayD R Borchelt, A Taraboulos, S B Prusiner
Biochemistry|December 15, 1987
Evidence for a secretory form of the cellular prion proteinB Hay, S B Prusiner, V R Lingappa
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1987
Purified prion proteins and scrapie infectivity copartition into liposomesR Gabizon, M P McKinley, S B Prusiner
Folding & Design|January 1, 1996
Scrapie prions: a three-dimensional model of an infectious fragmentZ Huang, S B Prusiner, F E Cohen
Archives of Virology. Supplementum|February 24, 2001
Quantitative traits of prion strains are enciphered in the conformation of the prion proteinJ Safar, F E Cohen, S B Prusiner
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