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Acta Neuropathologica Communications|May 22, 2019
Comparative analyses of the in vivo induction and transmission of α-synuclein pathology in transgenic mice by MSA brain lysate and recombinant α-synuclein fibrilsJess-Karan S Dhillon, Jorge A Trejo-Lopez, Cara Riffe, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 1995
Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cellsS Rabizadeh, E B Gralla, D R Borchelt, et al.
Neurobiology of Aging|January 24, 2002
Accumulation of proteolytic fragments of mutant presenilin 1 and accelerated amyloid deposition are co-regulated in transgenic miceDavid R Borchelt, Michael K Lee, Victoria Gonzales, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Polyglutamine pathogenesisC A Ross, J D Wood, G Schilling, et al.
Acta Neuropathologica Communications|April 20, 2022
Impact of APOE genotype on prion-type propagation of tauopathyTristan Williams, Alejandra Jolie Ruiz, Angelica Maria Ruiz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 8, 2019
PMP22 Regulates Cholesterol Trafficking and ABCA1-Mediated Cholesterol EffluxYe Zhou, Joshua R Miles, Hagai Tavori, et al.
Acta Neuropathologica Communications|December 20, 2018
Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3Christina Moloney, Sruti Rayaprolu, John Howard, et al.
Acta Neuropathologica Communications|June 19, 2023
Humanized APOE genotypes influence lifespan independently of tau aggregation in the P301S mouse model of tauopathyTristan Williams, Tim Bathe, Quan Vo, et al.
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