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The Journal of Biological Chemistry|June 13, 1997
In situ formation of protease-resistant prion protein in transmissible spongiform encephalopathy-infected brain slicesR A Bessen, G J Raymond, B CaugheyThe Journal of Biological Chemistry|November 21, 1998
Strain-dependent differences in beta-sheet conformations of abnormal prion proteinB Caughey, G J Raymond, R A BessenNature|June 22, 1995
Non-genetic propagation of strain-specific properties of scrapie prion proteinR A Bessen, D A Kocisko, G J Raymond, et al.Journal of Virology|February 1, 1993
Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cellsB Caughey, G J RaymondThe Journal of Biological Chemistry|September 25, 1991
The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitiveB Caughey, G J RaymondMolecular Biotechnology|August 10, 2000
Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems. An updateB Caughey, G J Raymond, S A Priola, et al.Journal of Virology|December 1, 1991
N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant stateB Caughey, G J Raymond, D Ernst, et al.Proceedings of the National Academy of Sciences of the United States of America|February 12, 1998
Chaperone-supervised conversion of prion protein to its protease-resistant formS K DebBurman, G J Raymond, B Caughey, et al.Infectious Agents and Disease|April 1, 1994
Prion protein and the scrapie agent: in vitro studies in infected neuroblastoma cellsS A Priola, B Caughey, G J Raymond, et al.Journal of Virology|October 3, 2001
Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humansR Race, A Raines, G J Raymond, et al.Pageof 70