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Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 7, 2003
Genomic characterization of the human prion protein (PrP) gene locusEleni Makrinou, John Collinge, Michael Antoniou
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.
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.
Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, 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.
Brain : a Journal of Neurology|October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseasesDurrenajaf Siddique, Harpreet Hyare, Stephen Wroe, et al.
Acta Neuropathologica|February 12, 2014
The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issuesIone O C Woollacott, Simon Mead
Brain : a Journal of Neurology|August 14, 2015
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 yearsPeter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
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