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Nature Communications|May 24, 2018
Intron retention and nuclear loss of SFPQ are molecular hallmarks of ALSRaphaelle Luisier, Giulia E Tyzack, Claire E Hall, et al.The Journal of Biological Chemistry|April 13, 2010
The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron diseaseAli Morsi El-Kadi, Virginie Bros-Facer, Wenhan Deng, et al.Current Rheumatology Reports|November 18, 2014
Ongoing developments in sporadic inclusion body myositisPedro M Machado, Mhoriam Ahmed, Stefen Brady, et al.Acta Neuropathologica|September 11, 2012
Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashionJacqueline C Mitchell, Philip McGoldrick, Caroline Vance, et al.Neurology(R) Neuroimmunology & Neuroinflammation|June 17, 2016
Systemic inflammatory response and neuromuscular involvement in amyotrophic lateral sclerosisChing-Hua Lu, Kezia Allen, Felicia Oei, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 11, 2014
Plasma neurofilament heavy chain levels and disease progression in amyotrophic lateral sclerosis: insights from a longitudinal studyChing-Hua Lu, Axel Petzold, Jo Topping, 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.Plos Genetics|March 10, 2015
HDAC4-myogenin axis as an important marker of HD-related skeletal muscle atrophyMichal Mielcarek, Marta Toczek, Cleo J L M Smeets, et al.Neurology|May 3, 2015
Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosisChing-Hua Lu, Corrie Macdonald-Wallis, Elizabeth Gray, et al.Human Molecular Genetics|July 7, 2009
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouseFrancesca E Mackenzie, Rosario Romero, Debbie Williams, et al.Pageof 12