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Acta Neuropathologica|April 17, 2026
A model-based prion vaccine protects a transgenic mouse line carrying a Gerstmann-Sträussler-Scheinker disease mutationAndrew Fang, Xinli Tang, Madeleine Fleming, et al.Molecular Neurodegeneration|February 19, 2013
Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohortsBadri Vardarajan, David Vergote, Fadel Tissir, et al.Nature Medicine|June 13, 2006
Cyclohexanehexol inhibitors of Abeta aggregation prevent and reverse Alzheimer phenotype in a mouse modelJoAnne McLaurin, Meredith E Kierstead, Mary E Brown, et al.Proceedings of the National Academy of Sciences of the United States of America|June 14, 2005
Dissociated phenotypes in presenilin transgenic mice define functionally distinct gamma-secretasesPeter Mastrangelo, Paul M Mathews, M Azhar Chishti, et al.EMBO Molecular Medicine|February 10, 2015
Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestationAgnes Lau, Alex McDonald, Nathalie Daude, et al.Brain : a Journal of Neurology|December 28, 2010
Reversal of autophagy dysfunction in the TgCRND8 mouse model of Alzheimer's disease ameliorates amyloid pathologies and memory deficitsDun-Sheng Yang, Philip Stavrides, Panaiyur S Mohan, et al.Autophagy|April 6, 2011
Therapeutic effects of remediating autophagy failure in a mouse model of Alzheimer disease by enhancing lysosomal proteolysisDun-Sheng Yang, Philip Stavrides, Panaiyur S Mohan, et al.Plos Pathogens|January 17, 2018
A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS allelesRobert C C Mercer, Nathalie Daude, Lyudmyla Dorosh, et al.The American Journal of Pathology|September 28, 2006
Cortical neuronal and glial pathology in TgTauP301L transgenic mice: neuronal degeneration, memory disturbance, and phenotypic variationTetsuro Murakami, Erwan Paitel, Takeshi Kawarabayashi, et al.Pageof 14