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The FEBS Journal|October 10, 2013
G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivoMelissa P Wu, Jamie R Doyle, Brenda Barry, et al.Skeletal Muscle|March 8, 2012
A novel whole-cell lysate kinase assay identifies substrates of the p38 MAPK in differentiating myoblastsJames Dr Knight, Ruijun Tian, Robin Ec Lee, et al.Ebiomedicine|April 28, 2020
Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophyMarc-Olivier Deguise, Yves De Repentigny, Alexandra Tierney, et al.Annals of Neurology|August 29, 2012
Glucose metabolism and pancreatic defects in spinal muscular atrophyMelissa Bowerman, Kathryn J Swoboda, John-Paul Michalski, et al.Ebiomedicine|November 8, 2024
Liver SMN restoration rescues the Smn2B/- mouse model of spinal muscular atrophyEmma R Sutton, Ariane Beauvais, Rebecca Yaworski, et al.Neurobiology of Disease|June 12, 2025
Modulation of miR-145 in a mouse model of multiple sclerosis: A promising approach to attenuate inflammation and degenerationMonique Marylin Alves de Almeida, Samantha F Kornfeld, Yves De Repentigny, et al.BMC Molecular Biology|July 22, 2017
Splicing arrays reveal novel RBM10 targets, including SMN2 pre-mRNALeslie C Sutherland, Philippe Thibault, Mathieu Durand, et al.Cellular and Molecular Gastroenterology and Hepatology|February 5, 2021
SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver DiseaseMarc-Olivier Deguise, Chantal Pileggi, Yves De Repentigny, et al.Biorxiv : the Preprint Server for Biology|January 30, 2023
Base editing as a genetic treatment for spinal muscular atrophyChristiano R R Alves, Leillani L Ha, Rebecca Yaworski, et al.Nature Biomedical Engineering|December 6, 2023
Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophyChristiano R R Alves, Leillani L Ha, Rebecca Yaworski, et al.Pageof 4