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Journal of Cell Science|July 2, 2013
Alternative fates of newly formed PrPSc upon prion conversion on the plasma membraneRob Goold, Chris McKinnon, Samira Rabbanian, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 11, 2009
Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfacesJulie Ann Edgeworth, Graham S Jackson, Anthony R Clarke, et al.
Neuroimage. Clinical|November 18, 2019
Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian processLiane S Canas, Carole H Sudre, Enrico De Vita, et al.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
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.
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