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Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrierD A Kocisko, S A Priola, G J Raymond, et al.
Nature|June 22, 1995
Non-genetic propagation of strain-specific properties of scrapie prion proteinR A Bessen, D A Kocisko, G J Raymond, et al.
Nature|August 11, 1994
Cell-free formation of protease-resistant prion proteinD A Kocisko, J H Come, S A Priola, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2000
Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapyK A Conway, S J Lee, J C Rochet, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|October 6, 2000
An improved method of preparing the amyloid beta-protein for fibrillogenesis and neurotoxicity experimentsY Fezoui, D M Hartley, J D Harper, et al.
Nature Structural Biology|November 1, 1995
Structural model for the beta-amyloid fibril based on interstrand alignment of an antiparallel-sheet comprising a C-terminal peptideP T Lansbury, P R Costa, J M Griffiths, et al.
Nature|July 17, 1997
Molecular assessment of the potential transmissibilities of BSE and scrapie to humansG J Raymond, J Hope, D A Kocisko, et al.
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