Shin'Ichi Takeda


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Person Info

NAME

Shin'Ichi

SURNAME

Takeda

Publications in SciGraph latest 50 shown

  • 2018-12 Author Correction: Direct reprogramming of fibroblasts into skeletal muscle progenitor cells by transcription factors enriched in undifferentiated subpopulation of satellite cells in SCIENTIFIC REPORTS
  • 2018-12 Publisher Correction: Direct reprogramming of fibroblasts into skeletal muscle progenitor cells by transcription factors enriched in undifferentiated subpopulation of satellite cells in SCIENTIFIC REPORTS
  • 2018-12 Premyogenic progenitors derived from human pluripotent stem cells expand in floating culture and differentiate into transplantable myogenic progenitors in SCIENTIFIC REPORTS
  • 2018-09-01 Exon Skipping Using Antisense Oligonucleotides for Laminin-Alpha2-Deficient Muscular Dystrophy in EXON SKIPPING AND INCLUSION THERAPIES
  • 2018-09-01 Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45–55 Skipping Accompanied by Rescue of Dystrophin Expression in EXON SKIPPING AND INCLUSION THERAPIES
  • 2018-09-01 In Vitro Multiexon Skipping by Antisense PMOs in Dystrophic Dog and Exon 7-Deleted DMD Patient in EXON SKIPPING AND INCLUSION THERAPIES
  • 2018-09-01 In Vivo Evaluation of Multiple Exon Skipping with Peptide-PMOs in Cardiac and Skeletal Muscles in Dystrophic Dogs in EXON SKIPPING AND INCLUSION THERAPIES
  • 2018-09-01 In Vivo Evaluation of Single-Exon and Multiexon Skipping in mdx52 Mice in EXON SKIPPING AND INCLUSION THERAPIES
  • 2018-08-28 Tbx1 regulates inherited metabolic and myogenic abilities of progenitor cells derived from slow- and fast-type muscle in CELL DEATH & DIFFERENTIATION
  • 2018 Exon Skipping Therapy Using Phosphorodiamidate Morpholino Oligomers in the mdx52 Mouse Model of Duchenne Muscular Dystrophy in DUCHENNE MUSCULAR DYSTROPHY
  • 2017-12 Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice in SKELETAL MUSCLE
  • 2017-12 Direct reprogramming of fibroblasts into skeletal muscle progenitor cells by transcription factors enriched in undifferentiated subpopulation of satellite cells in SCIENTIFIC REPORTS
  • 2017-02 Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy in CELL DEATH & DIFFERENTIATION
  • 2017 Systemic Delivery of Morpholinos to Skip Multiple Exons in a Dog Model of Duchenne Muscular Dystrophy in MORPHOLINO OLIGOMERS
  • 2016-12 Inflammatory predisposition predicts disease phenotypes in muscular dystrophy in INFLAMMATION AND REGENERATION
  • 2016-12 Subclinical growth of an arteriovenous fistula associated with renal biopsy: a case report in BMC NEPHROLOGY
  • 2016-12 Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network in BMC HEALTH SERVICES RESEARCH
  • 2016-07 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 in JOURNAL OF HUMAN GENETICS
  • 2016 Stem Cell-Based Therapy for Duchenne Muscular Dystrophy in TRANSLATIONAL RESEARCH IN MUSCULAR DYSTROPHY
  • 2015-12 Erratum: G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy in NATURE COMMUNICATIONS
  • 2015-12 Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A in SKELETAL MUSCLE
  • 2015-12 G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy in NATURE COMMUNICATIONS
  • 2015-12 A muscle-liver-fat signalling axis is essential for central control of adaptive adipose remodelling in NATURE COMMUNICATIONS
  • 2015-07 Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression in SCIENTIFIC REPORTS
  • 2014-12 Nationwide patient registry for GNE myopathy in Japan in ORPHANET JOURNAL OF RARE DISEASES
  • 2014-11 Three novel serum biomarkers, miR-1, miR-133a, and miR-206 for Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, and Becker muscular dystrophy in ENVIRONMENTAL HEALTH AND PREVENTIVE MEDICINE
  • 2014-02 Is calcium replacement therapy unnecessary for severe hypocalcemia associated with rhabdomyolysis? in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2013-12 Initial Pulmonary Respiration Causes Massive Diaphragm Damage and Hyper-CKemia in Duchenne Muscular Dystrophy Dog in SCIENTIFIC REPORTS
  • 2013-12 Manumycin A corrects aberrant splicing of Clcn1 in myotonic dystrophy type 1 (DM1) mice in SCIENTIFIC REPORTS
  • 2013-12 Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients in JOURNAL OF NEUROLOGY
  • 2013-12 Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy) in ORPHANET JOURNAL OF RARE DISEASES
  • 2013-08 A case of renal impairment after near-drowning: the universal nature of acute kidney injury in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2013-01 Activation of calcium signaling through Trpv1 by nNOS and peroxynitrite as a key trigger of skeletal muscle hypertrophy in NATURE MEDICINE
  • 2012-12 Four consecutive cases of Achilles tendon disorders associated with levofloxacin treatment in hemodialysis patients in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2012-10 Calcitonin receptor and Odz4 are differently expressed in Pax7-positive cells during skeletal muscle regeneration in JOURNAL OF MOLECULAR HISTOLOGY
  • 2011-10 Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy in NATURE
  • 2011-09 Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transduction in GENE THERAPY
  • 2011 Mechanobiology in Skeletal Muscle: Conversion of Mechanical Information into Molecular Signal in MECHANOSENSING BIOLOGY
  • 2010-12-08 Antisense Oligo-Mediated Multiple Exon Skipping in a Dog Model of Duchenne Muscular Dystrophy in MUSCLE GENE THERAPY
  • 2010-02 Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle in NATURE CELL BIOLOGY
  • 2009-06 CCN3 and bone marrow cells in JOURNAL OF CELL COMMUNICATION AND SIGNALING
  • 2009-02 Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene in JOURNAL OF HUMAN GENETICS
  • 2007-12 Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ) in BMC MUSCULOSKELETAL DISORDERS
  • 2007-09 Injection of a recombinant AAV serotype 2 into canine skeletal muscles evokes strong immune responses against transgene products in GENE THERAPY
  • 2006-12 Cardiac involvement in Beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies in BMC CARDIOVASCULAR DISORDERS
  • 2006-10 Identification and characterization of a novel human dysferlin transcript: dysferlin_v1 in HUMAN GENETICS
  • 2003-06 Green Fluorescent Protein-Transgenic Rat as a Tool for Study of Transplantation and Regeneration in Myocardium in CARDIOVASCULAR ENGINEERING
  • 2003-05 Cardiac-Restricted Ankyrin-Repeated Protein Is Differentially Induced in Duchenne and Congenital Muscular Dystrophy in LABORATORY INVESTIGATION
  • 2002-12 Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product in GENE THERAPY
  • 2001-10 Gene Therapy for Muscular Dystrophies in BIODRUGS
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