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The Biochemical Journal|July 11, 2006
A reassessment of copper(II) binding in the full-length prion proteinMark A Wells, Graham S Jackson, Samantha Jones, et al.Scientific Reports|January 25, 2019
Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitroCassandra Terry, Robert L Harniman, Jessica Sells, et al.Prion|June 11, 2016
Physical, chemical and kinetic factors affecting prion infectivityFrancesca Properzi, Anjna Badhan, Steffi Klier, et al.Brain : a Journal of Neurology|May 24, 2003
Molecular classification of sporadic Creutzfeldt-Jakob diseaseAndrew F Hill, Susan Joiner, Jonathan D F Wadsworth, et al.The Journal of Biological Chemistry|May 15, 2026
Prion propagation is controlled by discrete structural regions of PrP rather than overall stabilitySavroop K Bhamra, Parineeta Arora, May Liew, et al.Brain : a Journal of Neurology|February 11, 2020
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosisPhillip Smethurst, Emmanuel Risse, Giulia E Tyzack, et al.Biochimica Et Biophysica Acta|October 16, 2007
Beta-PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91-110 that recognise native PrPScAzadeh Khalili-Shirazi, Maria Kaisar, Gary Mallinson, et al.American Journal of Human Genetics|February 26, 2013
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK populationJon Beck, Mark Poulter, Davina Hensman, et al.Plos Pathogens|February 24, 2012
Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infectionRocio Castro-Seoane, Holger Hummerich, Trevor Sweeting, et al.Proceedings of the National Academy of Sciences of the United States of America|July 28, 2010
Spontaneous generation of mammalian prionsJulie A Edgeworth, Nathalie Gros, Jack Alden, et al.Pageof 36