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Scientific Reports|December 1, 2020
IL-10 based immunomodulation initiated at birth extends lifespan in a familial mouse model of amyotrophic lateral sclerosisMichael R Strickland, Kristen R Ibanez, Mariya Yaroshenko, et al.Glia|February 26, 2021
Reactive astrocytes as treatment targets in Alzheimer's disease-Systematic review of studies using the APPswePS1dE9 mouse modelTamar Smit, Natasja A C Deshayes, David R Borchelt, et al.Neuroscience Letters|January 24, 1997
In an epidemiological sample the apolipoprotein E4 allele is associated to dementia and loss of memory function only in the very oldR Gessner, F M Reischies, A Kage, et al.Neuron|April 3, 2003
APP processing and synaptic functionFlavio Kamenetz, Taisuke Tomita, Helen Hsieh, et al.Plos One|November 7, 2018
Loss of charge mutations in solvent exposed Lys residues of superoxide dismutase 1 do not induce inclusion formation in cultured cell modelsKeith Crosby, Anthony M Crown, Brittany L Roberts, et al.Acta Neuropathologica Communications|June 3, 2014
Conformational specificity of the C4F6 SOD1 antibody; low frequency of reactivity in sporadic ALS casesJacob I Ayers, Guilian Xu, Olga Pletnikova, et al.Acta Neuropathologica|September 29, 2014
Experimental transmissibility of mutant SOD1 motor neuron diseaseJacob I Ayers, Susan Fromholt, Morgan Koch, et al.Biomolecular Engineering|May 5, 2001
Co-expression of multiple transgenes in mouse CNS: a comparison of strategiesJ L Jankowsky, H H Slunt, T Ratovitski, et al.Human Molecular Genetics|October 12, 2014
Direct and indirect mechanisms for wild-type SOD1 to enhance the toxicity of mutant SOD1 in bigenic transgenic miceGuilian Xu, Jacob I Ayers, Brittany L Roberts, et al.Molecular Neurodegeneration|December 18, 2013
Features of wild-type human SOD1 limit interactions with misfolded aggregates of mouse G86R Sod1David A Qualls, Mercedes Prudencio, Brittany L T Roberts, et al.Pageof 28