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Journal of Virology|February 7, 2001
Cultured cell sublines highly susceptible to prion infectionP J Bosque, S B Prusiner
Annals of Neurology|April 1, 1994
Human prion diseasesS B Prusiner, K K Hsiao
Annual Review of Genetics|January 1, 1997
Genetics of prionsS B Prusiner, M R Scott
Brain Pathology (Zurich, Switzerland)|July 1, 1991
Molecular biology and pathology of scrapie and the prion diseases of humansS B Prusiner, S J DeArmond
Annual Review of Biochemistry|October 6, 1998
Pathologic conformations of prion proteinsF E Cohen, S B Prusiner
Brain Pathology (Zurich, Switzerland)|January 1, 1995
Prion protein transgenes and the neuropathology in prion diseasesS J DeArmond, S B Prusiner
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 29, 1994
Nucleic acids in prion preparations: unspecific background or essential component?K Kellings, S B Prusiner, D Riesner
Medicine|July 1, 1997
Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan JewsZ Meiner, R Gabizon, S B Prusiner
The Journal of Cell Biology|June 1, 1990
Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cellsA Taraboulos, D Serban, S B Prusiner
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