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Journal of Neurochemistry|April 29, 2005
Prion protein glycosylationVictoria A Lawson, Steven J Collins, Colin L Masters, et al.Lancet (London, England)|January 16, 2004
Transmissible spongiform encephalopathiesSteven J Collins, Victoria A Lawson, Colin L MastersMolecular Neurodegeneration|April 27, 2012
Prion subcellular fractionation reveals infectivity spectrum, with a high titre-low PrPres level disparityVictoria Lewis, Cathryn L Haigh, Colin L Masters, et al.Neurobiology of Disease|October 26, 2005
Extended period of asymptomatic prion disease after low dose inoculation: assessment of detection methods and implications for infection controlSteven J Collins, Victoria Lewis, Marcus W Brazier, et al.Journal of Neuropathology and Experimental Neurology|November 18, 2009
Increased proportions of C1 truncated prion protein protect against cellular M1000 prion infectionVictoria Lewis, Andrew F Hill, Cathryn L Haigh, et al.Cell Research|July 15, 2009
PrPC-related signal transduction is influenced by copper, membrane integrity and the alpha cleavage siteCathryn L Haigh, Victoria A Lewis, Laura J Vella, et al.The Journal of Biological Chemistry|August 30, 2012
The prion protein preference of sporadic Creutzfeldt-Jakob disease subtypesHelen M J Klemm, Jeremy M Welton, Colin L Masters, et al.Glycobiology|February 22, 2015
Glycosaminoglycan sulfation determines the biochemical properties of prion protein aggregatesLaura J Ellett, Bradley M Coleman, Mitch C Shambrook, et al.Annals of Neurology|September 27, 2002
Quinacrine does not prolong survival in a murine Creutzfeldt-Jakob disease modelSteven J Collins, Victoria Lewis, Marcus Brazier, et al.Journal of Virology|April 30, 2010
Residues surrounding the glycosylphosphatidylinositol anchor attachment site of PrP modulate prion infection: insight from the resistance of rabbits to prion diseaseRebecca M Nisbet, Christopher F Harrison, Victoria A Lawson, et al.Pageof 101