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Disease Models & Mechanisms|June 29, 2011
The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophyJames N Sleigh, Thomas H Gillingwater, Kevin TalbotJournal of Anatomy|May 31, 2008
Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degenerationBecki Baxter, Thomas H Gillingwater, Simon H ParsonJournal of Neuropathology and Experimental Neurology|August 10, 2006
Synaptic vulnerability in neurodegenerative diseaseThomas M Wishart, Simon H Parson, Thomas H GillingwaterNature Reviews. Neurology|February 10, 2018
Advances in therapy for spinal muscular atrophy: promises and challengesEwout J N Groen, Kevin Talbot, Thomas H GillingwaterNeuromuscular Disorders : NMD|July 28, 2016
Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophyHeidi R Fuller, Thomas H Gillingwater, Thomas M WishartNature Reviews. Neurology|January 1, 2025
Targeting common disease pathomechanisms to treat amyotrophic lateral sclerosisKiterie M E Faller, Helena Chaytow, Thomas H GillingwaterFrontiers in Molecular Neuroscience|March 20, 2019
Molecular Mechanisms Underlying Sensory-Motor Circuit Dysfunction in SMAHannah K Shorrock, Thomas H Gillingwater, Ewout J N GroenCellular and Molecular Life Sciences : CMLS|April 6, 2021
Revisiting the role of mitochondria in spinal muscular atrophyRachel James, Helena Chaytow, Leire M Ledahawsky, et al.Drugs|January 31, 2018
Overview of Current Drugs and Molecules in Development for Spinal Muscular Atrophy TherapyHannah K Shorrock, Thomas H Gillingwater, Ewout J N GroenAnatomical Sciences Education|January 7, 2012
Development of a supported self-directed learning approach for anatomy educationGordon S Findlater, Fanney Kristmundsdottir, Simon H Parson, et al.Pageof 17