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Plos One|May 26, 2017
Prion pathogenesis is unaltered in the absence of SIRPα-mediated "don't-eat-me" signalingMario Nuvolone, Marta Paolucci, Silvia Sorce, et al.Scientific Reports|October 24, 2024
Optimal control of discrete event systems under uncertain environment based on supervisory control theory and reinforcement learningYingjun Liu, Fuchun LiuJournal of Neurology|November 14, 2008
Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profilesKatharina Stoeck, Klaus Hess, Lorenz Amsler, et al.Journal of Neuroscience Research|February 17, 2007
Enhanced susceptibility of Prnp-deficient mice to kainate-induced seizures, neuronal apoptosis, and death: Role of AMPA/kainate receptorsAlejandra Rangel, Ferran Burgaya, Rosalina Gavín, et al.Brain Pathology (Zurich, Switzerland)|November 20, 2018
Genome-wide identification of microRNAs regulating the human prion proteinDaniel Pease, Claudia Scheckel, Elke Schaper, et al.Plos One|September 10, 2009
Functionally relevant domains of the prion protein identified in vivoFrank Baumann, Jens Pahnke, Ivan Radovanovic, et al.The Journal of Biological Chemistry|June 7, 2012
Multiple substitutions of methionine 129 in human prion protein reveal its importance in the amyloid fibrillation pathwaySofie Nyström, Rajesh Mishra, Simone Hornemann, et al.Journal of Neurology|March 2, 2005
Sporadic Creutzfeldt-Jakob disease: a comparison of pathological findings and diffusion weighted imagingHeike Russmann, Francois Vingerhoets, Judith Miklossy, et al.Acta Neuropathologica|March 9, 2006
Cerebrovascular P-glycoprotein expression is decreased in Creutzfeldt-Jakob diseaseSilke Vogelgesang, Markus Glatzel, Lary C Walker, et al.Frontiers in Microbiology|June 26, 2024
Longitudinal microbiome investigation throughout prion disease course reveals pre- and symptomatic compositional perturbations linked to short-chain fatty acid metabolism and cognitive impairment in miceMarco Losa, Yasser Morsy, Marc Emmenegger, et al.Pageof 57