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Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.The Biochemical Journal|September 15, 2005
Recombinant prion protein does not possess SOD-1 activitySamantha Jones, Mark Batchelor, Daljit Bhelt, et al.Journal of Neuropathology and Experimental Neurology|November 7, 2006
The human prion protein residue 129 polymorphism lies within a cluster of epitopes for T cell recognitionJeremy D Isaacs, Rebecca J Ingram, John Collinge, et al.Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, et al.Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.Nature Reviews. Disease Primers|February 29, 2024
Creutzfeldt-Jakob disease and other prion diseasesInga Zerr, Anna Ladogana, Simon Mead, et al.Proceedings of the National Academy of Sciences of the United States of America|July 18, 2008
Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion diseaseMelanie D White, Michael Farmer, Ilaria Mirabile, et al.The Journal of General Virology|November 19, 2010
A standardized comparison of commercially available prion decontamination reagents using the Standard Steel-Binding AssayJulie Ann Edgeworth, Anita Sicilia, Jackie Linehan, et al.Neuroscience Letters|April 15, 2004
Pathogenic human prion protein rescues PrP null phenotype in transgenic miceEmmanuel A Asante, Yuan-Gen Li, Ian Gowland, et al.Pageof 43