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Nature Aging|June 4, 2024
Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositisSven Wischnewski, Thomas Thäwel, Chiseko Ikenaga, et al.Nature Neuroscience|August 6, 2013
Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formationDongyi Xu, Weiping Shen, Rong Guo, et al.Science Translational Medicine|January 19, 2022
Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositisKyla A Britson, Jonathan P Ling, Kerstin E Braunstein, et al.Nature|August 27, 2015
The C9orf72 repeat expansion disrupts nucleocytoplasmic transportKe Zhang, Christopher J Donnelly, Aaron R Haeusler, et al.Neuron|April 7, 2017
Mutant Huntingtin Disrupts the Nuclear Pore ComplexJonathan C Grima, J Gavin Daigle, Nicolas Arbez, et al.Brain : a Journal of Neurology|August 28, 2015
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ geneOranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.Annals of the Rheumatic Diseases|August 25, 2022
Coexisting autoantibodies against transcription factor Sp4 are associated with decreased cancer risk in patients with dermatomyositis with anti-TIF1γ autoantibodiesYuji Hosono, Brandon Sie, Iago Pinal-Fernandez, et al.The Lancet. Neurology|September 22, 2023
Safety and efficacy of arimoclomol for inclusion body myositis: a multicentre, randomised, double-blind, placebo-controlled trialPedro M Machado, Michael P McDermott, Thomas Blaettler, et al.Scientific Reports|February 4, 2023
Coordinated local RNA overexpression of complement induced by interferon gamma in myositisMaria Casal-Dominguez, Iago Pinal-Fernandez, Katherine Pak, et al.Clinical and Experimental Rheumatology|February 10, 2023
Current status of clinical outcome measures in inclusion body myositis: a systematised reviewBhaskar Roy, Matteo Lucchini, James B Lilleker, et al.Pageof 12