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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.
Plos One|July 14, 2009
Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant miceGareth T Banks, Virginie Bros-Facer, Hazel P Williams, et al.
Human Molecular Genetics|March 27, 2014
Treatment with an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of Amyotrophic lateral sclerosisVirginie Bros-Facer, David Krull, Adam Taylor, 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.
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.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12Francesca Achilli, Shelagh Boyle, Dairin Kieran, et al.
Nature Neuroscience|October 29, 2021
Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosisIddo Magen, Nancy Sarah Yacovzada, Eran Yanowski, et al.
Neurology|May 13, 2014
Correlation of clinical and molecular features in spinal bulbar muscular atrophyPietro Fratta, Niranjanan Nirmalananthan, Luc Masset, 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.
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