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Department of Medical Genetics
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Impaired regenerative capacity and lower revertant fibre expansion in dystrophin-deficient mdx muscles on DBA/2 background.
Scientific reports Dec, 2016 | Pubmed ID: 27924830
Systemic Delivery of Morpholinos to Skip Multiple Exons in a Dog Model of Duchenne Muscular Dystrophy.
Methods in molecular biology (Clifton, N.J.) , 2017 | Pubmed ID: 28364245
LNA/DNA mixmer-based antisense oligonucleotides correct alternative splicing of the SMN2 gene and restore SMN protein expression in type 1 SMA fibroblasts.
Scientific reports Jun, 2017 | Pubmed ID: 28623256
Skipping Multiple Exons to Treat DMD-Promises and Challenges.
Biomedicines Jan, 2018 | Pubmed ID: 29301272
University of Alberta Faculty of Medicine and Dentistry
Joshua J. A. Lee1,
Rika Maruyama1,
Hidetoshi Sakurai2,
Toshifumi Yokota1
1Department of Medical Genetics, University of Alberta Faculty of Medicine and Dentistry,
2Center for iPS Cell Research and Application, Kyoto University
Aleksander Touznik1,
Toshifumi Yokota1,2
2Muscular Dystrophy Canada Research Chair, Department of Medical Genetics, University of Alberta Faculty of Medicine and Dentistry
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