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Yusuke Echigoya

University of Alberta
Nihon University

32

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630

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A Dystrophin Exon-52 Deleted Miniature Pig Model of Duchenne Muscular Dystrophy and Evaluation of Exon Skipping

2021 International Journal of Molecular Sciences
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Amelioration of intracellular Ca2+ regulation by exon-45 skipping in Duchenne muscular dystrophy-induced pluripotent stem cell-derived cardiomyocytes

2019 Biochemical and Biophysical Research Communications
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Exons 45-55 skipping using mutation-tailored cocktails of antisense morpholinos in the DMD gene

2019 Molecular Therapy
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Dystrophin-deficient cardiomyocyte derived from Duchenne Muscular Dystrophy specific induced pluripotent stem cells carrying the deletion of exon 46-55 in DMD gene

2017 Journal of the Neurological Sciences
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Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy

2017 Proceedings of the National Academy of Sciences of the United States of America
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Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy

2017 Molecular Therapy
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LNA/DNA mixmer-based antisense oligonucleotides correct alternative splicing of the SMN2 gene and restore SMN protein expression in type 1 SMA fibroblasts

2017 Scientific Reports
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Systemic Delivery of Morpholinos to Skip Multiple Exons in a Dog Model of Duchenne Muscular Dystrophy

2017 Methods of Molecular Biology
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Deletion of exons 3-9 encompassing a mutational hot spot in the DMD gene presents an asymptomatic phenotype, indicating a target region for multiexon skipping therapy.

2016 Journal of Human Genetics
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In Silico Screening Based on Predictive Algorithms as a Design Tool for Exon Skipping Oligonucleotides in Duchenne Muscular Dystrophy

2015 PLOS ONE
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Citations (34)