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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.
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.
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.
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.
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