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Biochemical Society Transactions|January 16, 2009
The role of CHMP2B in frontotemporal dementiaHazel Urwin, Shabnam Ghazi-Noori, John Collinge, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in miceJulia Grizenkova, Shaheen Akhtar, Holger Hummerich, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Neurobiology of Aging|June 5, 2018
Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
The Lancet. Neurology|January 24, 2026
Advances in biomarkers for diagnosis and prognosis of prion diseasesInga Zerr, Peter Hermann, Tze How Mok, et al.
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 5, 2011
How does the genetic assassin select its neuronal target?James C Stevens, Elizabeth M C Fisher, Simon Mead
Neuropathology and Applied Neurobiology|June 5, 2015
Review: an update on clinical, genetic and pathological aspects of frontotemporal lobar degenerationsTammaryn Lashley, Jonathan D Rohrer, Simon Mead, et al.
Molecular Medicine (Cambridge, Mass.)|February 12, 2005
Disease-associated prion protein elicits immunoglobulin M responses in vivoMourad Tayebi, Perry Enever, Zahid Sattar, et al.
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