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Molecular and Cellular Neurosciences|March 11, 2018
Assessment of metal concentrations in the SOD1G93A mouse model of amyotrophic lateral sclerosis and its potential role in muscular denervation, with particular focus on muscle tissueT Gabriel Enge, Heath Ecroyd, Dianne F Jolley, et al.Plos One|September 12, 2013
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosisSergey S Novoselov, Wendy J Mustill, Anna L Gray, et al.Neurobiology of Disease|May 21, 2018
Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitroEmma R Wilson, Umaiyal Kugathasan, Andrey Y Abramov, et al.Cell Death & Disease|May 24, 2018
Inhibiting p38 MAPK alpha rescues axonal retrograde transport defects in a mouse model of ALSKatherine L Gibbs, Bernadett Kalmar, Elena R Rhymes, et al.Eneuro|January 4, 2023
Microglial Expression of the Wnt Signaling Modulator DKK2 Differs between Human Alzheimer's Disease Brains and Mouse Neurodegeneration ModelsNozie D Aghaizu, Sarah Jolly, Satinder K Samra, et al.Human Molecular Genetics|June 9, 2017
Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth DiseaseBernadett Kalmar, Amy Innes, Klaus Wanisch, et al.Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2Alexander M Rossor, Gabrielle L Davidson, Julian Blake, et al.Human Molecular Genetics|October 3, 2014
Expression of a pathogenic mutation of SOD1 sensitizes aprataxin-deficient cells and mice to oxidative stress and triggers hallmarks of premature ageingJean Carroll, Tristan K W Page, Shih-Chieh Chiang, et al.Disease Models & Mechanisms|May 5, 2011
A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosisAbraham Acevedo-Arozena, Bernadett Kalmar, Shafa Essa, et al.Brain : a Journal of Neurology|January 18, 2022
Astrocytes display cell autonomous and diverse early reactive states in familial amyotrophic lateral sclerosisDoaa M Taha, Benjamin E Clarke, Claire E Hall, et al.Pageof 4