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The EMBO Journal|November 29, 2002
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinEmmanuel A Asante, Jacqueline M Linehan, Melanie Desbruslais, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2008
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The Journal of General Virology|July 9, 2010
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion proteinMalin K Sandberg, Huda Al-Doujaily, Christina J Sigurdson, et al.
The Journal of Pathology|February 5, 2011
Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence studyJonathan D F Wadsworth, Inmaculada Dalmau-Mena, Susan Joiner, et al.
Brain : a Journal of Neurology|August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneitySimon Mead, Mark Poulter, Jon Beck, et al.
Scientific Reports|May 8, 2015
A novel and rapid method for obtaining high titre intact prion strains from mammalian brainAdam Wenborn, Cassandra Terry, Nathalie Gros, et al.
Science (New York, N.Y.)|November 13, 2004
Human prion protein with valine 129 prevents expression of variant CJD phenotypeJonathan D F Wadsworth, Emmanuel A Asante, Melanie Desbruslais, et al.
Plos Pathogens|July 3, 2015
Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSSEmmanuel A Asante, Andrew Grimshaw, Michelle Smidak, et al.
Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2006
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous miceEmmanuel A Asante, Jacqueline M Linehan, Ian Gowland, et al.
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