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Cell Reports|December 8, 2022
Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategyShrestha Sinha Ray, Debdeep Dutta, Cassandra Dennys, et al.Skeletal Muscle|August 10, 2020
X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisationInès Barthélémy, Nadège Calmels, Robert B Weiss, et al.Annals of Neurology|January 23, 2015
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45Andrew R Findlay, Nicolas Wein, Yuuki Kaminoh, et al.Nature Medicine|August 11, 2014
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceNicolas Wein, Adeline Vulin, Maria S Falzarano, et al.Human Mutation|February 15, 2022
Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophyMegan A Waldrop, Steven A Moore, Katherine D Mathews, et al.Pageof 4