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The Lancet. Neurology|January 24, 2026
Genetic causes and modifiers of prion diseasesSimon Mead, Peter Hermann, Tze How Mok, et al.BMC Medical Genetics|September 17, 2009
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10qSarah E Lloyd, Martin Rossor, Nick Fox, et al.JAMA Neurology|May 24, 2013
Autoantibodies in sporadic Creutzfeldt-Jakob diseaseHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.Journal of Lipid Research|July 21, 2016
Pulmonary epithelial cancer cells and their exosomes metabolize myeloid cell-derived leukotriene C4 to leukotriene D4Ana Lukic, Jie Ji, Helena Idborg, et al.International Psychogeriatrics|October 25, 2018
The most problematic symptoms of prion disease - an analysis of carer experiencesLiz Ford, Peter Rudge, Kathy Robinson, et al.European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 23, 2017
GM-CSF- and M-CSF-primed macrophages present similar resolving but distinct inflammatory lipid mediator signaturesAna Lukic, Pia Larssen, Alexander Fauland, et al.Nature Reviews. Disease Primers|February 29, 2024
Creutzfeldt-Jakob disease and other prion diseasesInga Zerr, Anna Ladogana, Simon Mead, et al.JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.Proceedings of the National Academy of Sciences of the United States of America|March 30, 2020
Dicer up-regulation by inhibition of specific proteolysis in differentiating monocytic cellsDevaraj Basavarajappa, Stella Uebbing, Marius Kreiss, et al.Pageof 22