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Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, 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.Journal of Neurovirology|April 23, 2003
Prion diseasesEdward McKintosh, Sarah J Tabrizi, John CollingeNature|September 11, 2015
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.Neuroimage. Clinical|December 13, 2016
Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry studyEnrico De Vita, Gerard R Ridgway, Mark J White, et al.The New England Journal of Medicine|November 20, 2009
A novel protective prion protein variant that colocalizes with kuru exposureSimon Mead, Jerome Whitfield, Mark Poulter, et al.Journal of Alzheimer'S Disease : JAD|July 4, 2025
Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157Leah Holm-Mercer, Tze How Mok, Danielle Sequeira, et al.Nature Clinical Practice. Neurology|July 24, 2008
Mapping the progression of progranulin-associated frontotemporal lobar degenerationJonathan D Rohrer, Jason D Warren, Josephine Barnes, et al.Neurobiology of Aging|May 19, 2009
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationSara Rollinson, Jonathan D Rohrer, Julie van der Zee, et al.Biological Psychiatry|January 15, 2018
Prion Protein as a Toxic Acceptor of Amyloid-β OligomersSilvia A Purro, Andrew J Nicoll, John CollingePageof 35