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Plos One|November 5, 2011
The FSHD atrophic myotube phenotype is caused by DUX4 expressionCéline Vanderplanck, Eugénie Ansseau, Sébastien Charron, et al.Genomics|August 1, 1992
A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1A H Beggs, H A Phillips, H Kozman, et al.Neuromuscular Disorders : NMD|August 22, 2006
Induced dystrophin exon skipping in human muscle explantsG McClorey, A M Fall, H M Moulton, et al.Cellular and Molecular Life Sciences : CMLS|September 11, 2020
NEAT1 polyA-modulating antisense oligonucleotides reveal opposing functions for both long non-coding RNA isoforms in neuroblastomaAlina Naveed, Jack A Cooper, Ruohan Li, et al.Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.Scientific Reports|November 13, 2023
Induced alternative splicing an opportunity to study PCSK9 protein isoforms at physiologically relevant concentrationsJessica M Cale, Kristin A Ham, Dunhui Li, et al.International Journal of Experimental Pathology|November 12, 2013
Primary over-expression of AβPP in muscle does not lead to the development of inclusion body myositis in a new lineage of the MCK-AβPP transgenic mouseYue-Bei Luo, Russell D Johnsen, Lisa Griffiths, et al.Scientific Reports|July 24, 2021
Induction of cryptic pre-mRNA splice-switching by antisense oligonucleotidesKristin A Ham, Niall P Keegan, Craig S McIntosh, et al.Molecular Therapy. Nucleic Acids|January 25, 2013
Targeted exon skipping to address "leaky" mutations in the dystrophin geneSue Fletcher, Carl F Adkin, Penny Meloni, et al.Journal of Neuroimmunology|September 18, 2013
Complement-mediated muscle cell lysis: a possible mechanism of myonecrosis in anti-SRP associated necrotizing myopathy (ASANM)Arada Rojana-udomsart, Chalermchai Mitrpant, Christine Bundell, et al.Pageof 19