Search Results1-4 of  4

  • Yokota Toshifumi ID: 9000329423418

    Articles in CiNii:1

    • 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)
  • Yokota Toshifumi ID: 9000356596698

    Articles in CiNii:1

    • Comparison of the phenotypes of patients harboring in-frame deletions starting at exon 45 in the Duchenne muscular dystrophy gene indicates potential for the development of exon skipping therapy (2017)
  • YOKOTA Toshifumi ID: 9000020093205

    Department of Molecular Genetics, National Institute of Neuroscience, National Center of Neurology and Psychiatry|Department of Biological Sciences, Graduate School of Science, University of Tokyo (2000 from CiNii)

    Articles in CiNii:1

    • Aquaporin-4 is absent at the sarcolemma and at perivascular astrocyte endfeet in α1-syntrophin knockout mice (2000)
  • Yokota Toshifumi ID: 9000345403582

    Department of Medical Genetics, School of Human Development, Faculty of Medicine and Dentistry, University of Alberta|Muscular Dystrophy Canada Research Chair, University of Alberta (2016 from CiNii)

    Articles in CiNii:1

    • Targeting mRNA for the treatment of facioscapulohumeral muscular dystrophy (2016)
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