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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|April 30, 1999
Prion protein and species barriers in the transmissible spongiform encephalopathiesS A PriolaJournal of Virology|December 1, 1995
A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cellsS A Priola, B ChesebroMolecular Neurobiology|April 1, 1994
Inhibition of scrapie-associated PrP accumulation. Probing the role of glycosaminoglycans in amyloidogenesisS A Priola, B CaugheyThe Journal of Biological Chemistry|June 13, 1998
Abnormal properties of prion protein with insertional mutations in different cell typesS A Priola, B ChesebroThe EMBO Journal|December 1, 2001
Glycosylation influences cross-species formation of protease-resistant prion proteinS A Priola, V A LawsonVirology|June 1, 1991
The 5' and 3' limits of transcription in the pseudorabies virus latency associated transcription unitS A Priola, J G StevensCellular and Molecular Neurobiology|June 5, 2002
Antiaggregating antibody raised against human PrP 106-126 recognizes pathological and normal isoforms of the whole prion proteinE Hanan, S A Priola, B SolomonJournal of Virology|April 20, 2001
Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155S A Priola, J Chabry, K ChanJournal of Virology|October 3, 2001
Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoformI Vorberg, K Chan, S A PriolaArchives of Virology. Supplementum|December 17, 2005
Species barriers in prion diseases--brief reviewR A Moore, I Vorberg, S A PriolaPageof 3