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Science (New York, N.Y.)|January 7, 2012
PrP antibodies do not trigger mouse hippocampal neuron apoptosisPeter-Christian Klöhn, Michael Farmer, Jacqueline M Linehan, et al.Acta Neuropathologica|December 10, 2015
Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin-proteasome systemChris McKinnon, Rob Goold, Ralph Andre, et al.Journal of the Neurological Sciences|February 7, 2018
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion proteinSusan Joiner, Emmanuel A Asante, Jacqueline M Linehan, et al.Acta Neuropathologica Communications|November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseasesLilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.Lancet (London, England)|December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case reportStephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.The EMBO Journal|November 21, 2009
Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypesThomas S Jacques, Alexander Swales, Monika J Brzozowski, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.Pageof 5