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Annals of Neurology|July 16, 2026
Maternal-Fetal Administration of Risdiplam Partially Rescues the SMNΔ7 Mouse Model of Spinal Muscular AtrophyEmma R Sutton, Ariane Beauvais, Rebecca Yaworski, et al.
Elife|February 20, 2025
Impact of liver-specific survival motor neuron (SMN) depletion on central nervous system and peripheral tissue pathologyMonique Marylin Alves de Almeida, Yves De Repentigny, Sabrina Gagnon, et al.
Journal of Neuromuscular Diseases|February 20, 2025
Peripheral defects precede neuromuscular pathology in the Smn mouse model of spinal muscular atrophyAoife Reilly, Ariane Beauvais, Majd Al-Aarg, 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.
Human Molecular Genetics|November 10, 2023
A transcriptomics-based drug repositioning approach to identify drugs with similar activities for the treatment of muscle pathologies in spinal muscular atrophy (SMA) modelsJoseph M Hoolachan, Eve McCallion, Emma R Sutton, et al.
Skeletal Muscle|July 28, 2022
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy miceKatharina E Meijboom, Emma R Sutton, Eve McCallion, et al.
Skeletal Muscle|October 13, 2024
Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse modelGareth Hazell, Eve McCallion, Nina Ahlskog, et al.
Scientific Reports|November 17, 2025
Mifepristone alone and in combination with scAAV9-SMN1 gene therapy improves disease phenotypes in Smn2B/- spinal muscular atrophy miceEmma R Sutton, Eve McCallion, Joseph M Hoolachan, 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.
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