Shin'ichi Takeda

Department of Molecular Therapy, National Center of Neurology and Psychiatry

Affiliated withNational Center of Neurology and Psychiatry

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 23	2016
Publication title	2020

Other Publications

Article	Year
Intracellular cell-autonomous association of Notch and its ligands: a novel mechanism of Notch signal modification. Developmental biology\| PubMed ID: 11784114	2002
Interleukin 6 induces overexpression of the sarcolemmal utrophin in neonatal mdx skeletal muscle. Human gene therapy\| PubMed ID: 11874629	2002
Muscle regeneration by reconstitution with bone marrow or fetal liver cells from green fluorescent protein-gene transgenic mice. Journal of cell science\| PubMed ID: 11884527	2002
Effects of microgravity on myogenic factor expressions during postnatal development of rat skeletal muscle. Journal of applied physiology (Bethesda, Md. : 1985)\| PubMed ID: 11960943	2002
Progression of dystrophic features and activation of mitogen-activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice. FEBS letters\| PubMed ID: 12044863	2002
Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene. Biochemical and biophysical research communications\| PubMed ID: 12054513	2002
Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle. Human molecular genetics\| PubMed ID: 12095914	2002
Alpha1-syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration. The Journal of cell biology\| PubMed ID: 12221071	2002
Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice. Biochimica et biophysica acta\| PubMed ID: 12393173	2002
Canine X-linked muscular dystrophy in Japan (CXMDJ). Experimental animals / Japanese Association for Laboratory Animal Science\| PubMed ID: 12806883	2003
Expression profiling of cytokines and related genes in regenerating skeletal muscle after cardiotoxin injection: a role for osteopontin. The American journal of pathology\| PubMed ID: 12819025	2003
Negamycin restores dystrophin expression in skeletal and cardiac muscles of mdx mice. Journal of biochemistry\| PubMed ID: 14688241	2003
Skeletal muscle gene expression in space-flown rats. FASEB journal : official publication of the Federation of American Societies for Experimental Biology\| PubMed ID: 14715702	2004
Alpha1-syntrophin modulates turnover of ABCA1. The Journal of biological chemistry\| PubMed ID: 14722086	2004
[Gene therapy for muscular dystrophy]. No to hattatsu. Brain and development\| PubMed ID: 15031985	2004
Purification and cell-surface marker characterization of quiescent satellite cells from murine skeletal muscle by a novel monoclonal antibody. Experimental cell research\| PubMed ID: 15149854	2004
Identification and characterization of epsilon-sarcoglycans in the central nervous system. Brain research. Molecular brain research\| PubMed ID: 15193417	2004
Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice. Human molecular genetics\| PubMed ID: 15213105	2004
Mac-1(low) early myeloid cells in the bone marrow-derived SP fraction migrate into injured skeletal muscle and participate in muscle regeneration. Biochemical and biophysical research communications\| PubMed ID: 15358135	2004
Development of a safe oral Abeta vaccine using recombinant adeno-associated virus vector for Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 15505369	2004
AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 15509500	2004
The utrophin promoter A drives high expression of the transgenic LacZ gene in liver, testis, colon, submandibular gland, and small intestine. The journal of gene medicine\| PubMed ID: 15538725	2005
[Current status and perspective of gene therapy on dystrophic animal model]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 15651329	2004
Epsilon-sarcoglycan compensates for lack of alpha-sarcoglycan in a mouse model of limb-girdle muscular dystrophy. Human molecular genetics\| PubMed ID: 15689353	2005
Coordinate control of axon defasciculation and myelination by laminin-2 and -8. The Journal of cell biology\| PubMed ID: 15699217	2005
Participation of bone marrow-derived cells in fibrotic changes in denervated skeletal muscle. The American journal of pathology\| PubMed ID: 15920157	2005
Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise. Biochimica et biophysica acta\| PubMed ID: 15949699	2005
Functional heterogeneity of side population cells in skeletal muscle. Biochemical and biophysical research communications\| PubMed ID: 16455057	2006
Intracellular localization of dysferlin and its association with the dihydropyridine receptor. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases\| PubMed ID: 16550931	2005
Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases\| PubMed ID: 16550932	2005
Zeta-sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex. Experimental cell research\| PubMed ID: 16635485	2006
Ubiquitin ligase Cbl-b downregulates bone formation through suppression of IGF-I signaling in osteoblasts during denervation. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research\| PubMed ID: 16734387	2006
Expansion of revertant fibers in dystrophic mdx muscles reflects activity of muscle precursor cells and serves as an index of muscle regeneration. Journal of cell science\| PubMed ID: 16757519	2006
Identification and characterization of a novel human dysferlin transcript: dysferlin_v1. Human genetics\| PubMed ID: 16896923	2006
Cardiac involvement in Beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies. BMC cardiovascular disorders\| PubMed ID: 17140458	2006
Cardiac side population cells have a potential to migrate and differentiate into cardiomyocytes in vitro and in vivo. The Journal of cell biology\| PubMed ID: 17261849	2007
[Stem cell based cell therapy for muscular dystrophy]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 17432228	2006
[Therapeutic strategy for muscular dystrophies]. Brain and nerve = Shinkei kenkyū no shinpo\| PubMed ID: 17447528	2007
Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ). BMC musculoskeletal disorders\| PubMed ID: 17598883	2007
Molecular signature of quiescent satellite cells in adult skeletal muscle. Stem cells (Dayton, Ohio)\| PubMed ID: 17600112	2007
Deficiency of Cbl-b gene enhances infiltration and activation of macrophages in adipose tissue and causes peripheral insulin resistance in mice. Diabetes\| PubMed ID: 17601987	2007
Autologous transplantation of SM/C-2.6(+) satellite cells transduced with micro-dystrophin CS1 cDNA by lentiviral vector into mdx mice. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 17726457	2007
NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS. The Journal of clinical investigation\| PubMed ID: 17786240	2007
Transgenic expression of a myostatin inhibitor derived from follistatin increases skeletal muscle mass and ameliorates dystrophic pathology in mdx mice. FASEB journal : official publication of the Federation of American Societies for Experimental Biology\| PubMed ID: 17893249	2008
CD90-positive cells, an additional cell population, produce laminin alpha2 upon transplantation to dy(3k)/dy(3k) mice. Experimental cell research\| PubMed ID: 17963748	2008
Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 18261911	2008
Downstream utrophin enhancer is required for expression of utrophin in skeletal muscle. The journal of gene medicine\| PubMed ID: 18338831	2008
Selective vacuolar degeneration in dystrophin-deficient canine Purkinje fibers despite preservation of dystrophin-associated proteins with overexpression of Dp71. Circulation\| PubMed ID: 18458171	2008
The ubiquitin ligase gene (WWP1) is responsible for the chicken muscular dystrophy. FEBS letters\| PubMed ID: 18501710	2008
Recombinant adeno-associated virus type 8-mediated extensive therapeutic gene delivery into skeletal muscle of alpha-sarcoglycan-deficient mice. Human gene therapy\| PubMed ID: 18578595	2008
Muscle CD31(-) CD45(-) side population cells promote muscle regeneration by stimulating proliferation and migration of myoblasts. The American journal of pathology\| PubMed ID: 18669618	2008
Predominant localization of EFA6A, a guanine nucleotide exchange factor for ARF6, at the perisynaptic photoreceptor processes. Brain research\| PubMed ID: 18708035	2008
Suppression of macrophage functions impairs skeletal muscle regeneration with severe fibrosis. Experimental cell research\| PubMed ID: 18775697	2008
MicroRNA-206 is highly expressed in newly formed muscle fibers: implications regarding potential for muscle regeneration and maturation in muscular dystrophy. Cell structure and function\| PubMed ID: 18827405	2008
A deficit of brain dystrophin impairs specific amygdala GABAergic transmission and enhances defensive behaviour in mice. Brain : a journal of neurology\| PubMed ID: 18927146	2009
Transduction efficiency and immune response associated with the administration of AAV8 vector into dog skeletal muscle. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 18941441	2009
Hepcidin, an antimicrobial peptide is downregulated in ceruloplasmin-deficient mice. Peptides\| PubMed ID: 18948155	2009
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy. Human molecular genetics\| PubMed ID: 19017726	2009
Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro. Mechanisms of development\| PubMed ID: 19114101	2009
A renaissance for antisense oligonucleotide drugs in neurology: exon skipping breaks new ground. Archives of neurology\| PubMed ID: 19139297	2009
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene. Journal of human genetics\| PubMed ID: 19158820	2009
Generation of transplantable, functional satellite-like cells from mouse embryonic stem cells. FASEB journal : official publication of the Federation of American Societies for Experimental Biology\| PubMed ID: 19168704	2009
Exon-skipping therapy for Duchenne muscular dystrophy. Neuropathology : official journal of the Japanese Society of Neuropathology\| PubMed ID: 19486303	2009
Scalable purification of adeno-associated virus serotype 1 (AAV1) and AAV8 vectors, using dual ion-exchange adsorptive membranes. Human gene therapy\| PubMed ID: 19534598	2009
Ubiquitin ligase Cbl-b is a negative regulator for insulin-like growth factor 1 signaling during muscle atrophy caused by unloading. Molecular and cellular biology\| PubMed ID: 19546233	2009
CCN3 and bone marrow cells. Journal of cell communication and signaling\| PubMed ID: 19626464	2009
Evaluation of dystrophic dog pathology by fat-suppressed T2-weighted imaging. Muscle & nerve\| PubMed ID: 19670324	2009
Age-dependent expression of hephaestin in the brain of ceruloplasmin-deficient mice. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)\| PubMed ID: 19747625	2009
[Exon skipping therapy for Duchenne muscular dystrophy by using antisense Morpholino]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 20030230	2009
Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle. Nature cell biology\| PubMed ID: 20081842	2010
Efficient gene transfer into neurons in monkey brain by adeno-associated virus 8. Neuroreport\| PubMed ID: 20224455	2010
Genetic background affects properties of satellite cells and mdx phenotypes. The American journal of pathology\| PubMed ID: 20304955	2010
Neuronal NOS is dislocated during muscle atrophy in amyotrophic lateral sclerosis. Journal of the neurological sciences\| PubMed ID: 20435320	2010
Gene therapy for muscle disease. Experimental cell research\| PubMed ID: 20580709	2010
Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization. The Journal of biological chemistry\| PubMed ID: 20682766	2010
Progress in muscular dystrophy research with special emphasis on gene therapy. Proceedings of the Japan Academy. Series B, Physical and biological sciences\| PubMed ID: 20689232	2010
Six family genes control the proliferation and differentiation of muscle satellite cells. Experimental cell research\| PubMed ID: 20696153	2010
Antisense PMO found in dystrophic dog model was effective in cells from exon 7-deleted DMD patient. PloS one\| PubMed ID: 20805873	2010
In-frame dystrophin following exon 51-skipping improves muscle pathology and function in the exon 52-deficient mdx mouse. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 20823833	2010
[Molecular therapy for muscular dystrophy]. Nihon rinsho. Japanese journal of clinical medicine\| PubMed ID: 20976941	2010
The status of exon skipping as a therapeutic approach to duchenne muscular dystrophy. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 20978473	2011
Antisense oligo-mediated multiple exon skipping in a dog model of duchenne muscular dystrophy. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21194037	2011
SynArfGEF is a guanine nucleotide exchange factor for Arf6 and localizes preferentially at post-synaptic specializations of inhibitory synapses. Journal of neurochemistry\| PubMed ID: 21198641	2011
Mammalian models of Duchenne Muscular Dystrophy: pathological characteristics and therapeutic applications. Journal of biomedicine & biotechnology\| PubMed ID: 21274260	2011
Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers. Human molecular genetics\| PubMed ID: 21320869	2011
Synthesis of 2'-O-[2-(N-methylcarbamoyl)ethyl]ribonucleosides using oxa-Michael reaction and chemical and biological properties of oligonucleotide derivatives incorporating these modified ri... The Journal of organic chemistry\| PubMed ID: 21425877	2011
Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice. Molecular and cellular neurosciences\| PubMed ID: 21447391	2011
Current status of pharmaceutical and genetic therapeutic approaches to treat DMD. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 21468001	2011
Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy. PloS one\| PubMed ID: 21479190	2011
Medium-range correlation of Ag ions in superionic melts of Ag2Se and AgI by reverse Monte Carlo structural modelling-connectivity and void distribution. Journal of physics. Condensed matter : an Institute of Physics journal\| PubMed ID: 21613697	2011
Comparison of partial structures of melts of superionic AgI and CuI and non-superionic AgCl. Journal of physics. Condensed matter : an Institute of Physics journal\| PubMed ID: 21694124	2007
Restoring dystrophin expression in duchenne muscular dystrophy muscle progress in exon skipping and stop codon read through. The American journal of pathology\| PubMed ID: 21703390	2011
Exon-skipping therapy for Duchenne muscular dystrophy. Lancet (London, England)\| PubMed ID: 21784507	2011
The structure of molten CuCl, CuI and their mixtures as investigated by using neutron diffraction. Journal of physics. Condensed matter : an Institute of Physics journal\| PubMed ID: 21817319	2009
[Derivation of engraftable myogenic precursors from murine ES/iPS cells and generation of disease-specific iPS cells from patients with Duchenne muscular dystrophy (DMD) and other diseases]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 21921492	2010
Long-term engraftment of multipotent mesenchymal stromal cells that differentiate to form myogenic cells in dogs with Duchenne muscular dystrophy. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 21934652	2012
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy. Nature\| PubMed ID: 21979053	2011
Hesr1 and Hesr3 are essential to generate undifferentiated quiescent satellite cells and to maintain satellite cell numbers. Development (Cambridge, England)\| PubMed ID: 21989910	2011
Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle. Journal of cell science\| PubMed ID: 22045730	2011
Reprogramming efficiency and quality of induced Pluripotent Stem Cells (iPSCs) generated from muscle-derived fibroblasts of mdx mice at different ages. PLoS currents\| PubMed ID: 22101343	2011
Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dog. The journal of gene medicine\| PubMed ID: 22144143	2011
[Induced pluripotent stem (iPS) cell-based cell therapy for muscular dystrophy: current progress and future prospects]. Brain and nerve = Shinkei kenkyū no shinpo\| PubMed ID: 22223500	2012
[Exon-skipping therapy for Duchenne muscular dystrophy]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 22277414	2011
Slow-dividing satellite cells retain long-term self-renewal ability in adult muscle. Journal of cell science\| PubMed ID: 22349695	2012
Protein-anchoring strategy for delivering acetylcholinesterase to the neuromuscular junction. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 22371845	2012
Calcitonin receptor and Odz4 are differently expressed in Pax7-positive cells during skeletal muscle regeneration. Journal of molecular histology\| PubMed ID: 22562803	2012
Laminin regulates postnatal oligodendrocyte production by promoting oligodendrocyte progenitor survival in the subventricular zone. Glia\| PubMed ID: 22706957	2012
Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense delivery. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 22869723	2012
Extensive and prolonged restoration of dystrophin expression with vivo-morpholino-mediated multiple exon skipping in dystrophic dogs. Nucleic acid therapeutics\| PubMed ID: 22888777	2012
A conserved regulatory element located far downstream of the gls locus modulates gls expression through chromatin loop formation during myogenesis. FEBS letters\| PubMed ID: 22979984	2012
Activation of calcium signaling through Trpv1 by nNOS and peroxynitrite as a key trigger of skeletal muscle hypertrophy. Nature medicine\| PubMed ID: 23202294	2013
Identification of disease specific pathways using in vivo SILAC proteomics in dystrophin deficient mdx mouse. Molecular & cellular proteomics : MCP\| PubMed ID: 23297347	2013
Imatinib attenuates severe mouse dystrophy and inhibits proliferation and fibrosis-marker expression in muscle mesenchymal progenitors. Neuromuscular disorders : NMD\| PubMed ID: 23313020	2013
Prognostic impact of left ventricular noncompaction in patients with Duchenne/Becker muscular dystrophy--prospective multicenter cohort study. International journal of cardiology\| PubMed ID: 23333368	2013
Translating the genomics revolution: the need for an international gene therapy consortium for monogenic diseases. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 23369965	2013
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression. Human molecular genetics\| PubMed ID: 23562821	2013
Capsaicin mimics mechanical load-induced intracellular signaling events: involvement of TRPV1-mediated calcium signaling in induction of skeletal muscle hypertrophy. Channels (Austin, Tex.)\| PubMed ID: 23584166	2013
Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy). Orphanet journal of rare diseases\| PubMed ID: 23601510	2013
Robust Long-term Transduction of Common Marmoset Neuromuscular Tissue With rAAV1 and rAAV9. Molecular therapy. Nucleic acids\| PubMed ID: 23715217	2013
Manumycin A corrects aberrant splicing of Clcn1 in myotonic dystrophy type 1 (DM1) mice. Scientific reports\| PubMed ID: 23828222	2013
Initial pulmonary respiration causes massive diaphragm damage and hyper-CKemia in Duchenne muscular dystrophy dog. Scientific reports\| PubMed ID: 23851606	2013
Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice. Human molecular genetics\| PubMed ID: 23882132	2013
α1-Syntrophin-deficient mice exhibit impaired muscle force recovery after osmotic shock. Muscle & nerve\| PubMed ID: 24037898	2014
Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients. Journal of neurology\| PubMed ID: 24057148	2013
Inter-molecular correlations in liquid Se2Br2. Journal of physics. Condensed matter : an Institute of Physics journal\| PubMed ID: 24140925	2013
Current Challenges and Future Directions in Recombinant AAV-Mediated Gene Therapy of Duchenne Muscular Dystrophy. Pharmaceuticals (Basel, Switzerland)\| PubMed ID: 24276316	2013
Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains. Glycobiology\| PubMed ID: 24352591	2014
Dystrophic mdx mice develop severe cardiac and respiratory dysfunction following genetic ablation of the anti-inflammatory cytokine IL-10. Human molecular genetics\| PubMed ID: 24659498	2014
Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients. Human molecular genetics\| PubMed ID: 25027324	2014
Neuromuscular disease. DOK7 gene therapy benefits mouse models of diseases characterized by defects in the neuromuscular junction. Science (New York, N.Y.)\| PubMed ID: 25237101	2014
Nationwide patient registry for GNE myopathy in Japan. Orphanet journal of rare diseases\| PubMed ID: 25303967	2014
Doublecortin marks a new population of transiently amplifying muscle progenitor cells and is required for myofiber maturation during skeletal muscle regeneration. Development (Cambridge, England)\| PubMed ID: 25480916	2015
[Infrastructure for the clinical research of muscular dystrophies: remudy and MDCTN]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 25519964	2014
Intra-amniotic rAAV-mediated microdystrophin gene transfer improves canine X-linked muscular dystrophy and may induce immune tolerance. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 25586688	2015
Low intensity training of mdx mice reduces carbonylation and increases expression levels of proteins involved in energy metabolism and muscle contraction. Free radical biology & medicine\| PubMed ID: 25660994	2015
Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression. Scientific reports\| PubMed ID: 25661440	2015
Doublecortin marks a new population of transiently amplifying muscle progenitor cells and is required for myofiber maturation during skeletal muscle regeneration. Development (Cambridge, England)\| PubMed ID: 25670800	2015
[Exon skipping approach to Duchenne muscular dystorphy]. Rinshō shinkeigaku = Clinical neurology\| PubMed ID: 25672711	2014
A muscle-liver-fat signalling axis is essential for central control of adaptive adipose remodelling. Nature communications\| PubMed ID: 25827749	2015
G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy. Nature communications\| PubMed ID: 25865621	2015
Prognostic impact of venous thromboembolism in patients with Duchenne muscular dystrophy: Prospective multicenter 5-year cohort study. International journal of cardiology\| PubMed ID: 25965627	2015
Muscle Satellite Cell Protein Teneurin-4 Regulates Differentiation During Muscle Regeneration. Stem cells (Dayton, Ohio)\| PubMed ID: 26013034	2015
Erratum: G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy. Nature communications\| PubMed ID: 26084207	2015
Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy. Biochimica et biophysica acta\| PubMed ID: 26170062	2015
Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains. Brain sciences\| PubMed ID: 26230713	2015
Characterization of WWP1 protein expression in skeletal muscle of muscular dystrophy chickens. Journal of biochemistry\| PubMed ID: 26314333	2016
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A. Skeletal muscle\| PubMed ID: 26347253	2015
Calcitonin Receptor Signaling Inhibits Muscle Stem Cells from Escaping the Quiescent State and the Niche. Cell reports\| PubMed ID: 26440893	2015
A Disintegrin and Metalloprotease 10 (ADAM10) Is Indispensable for Maintenance of the Muscle Satellite Cell Pool. The Journal of biological chemistry\| PubMed ID: 26453297	2015
Trends in steroid therapy for Duchenne muscular dystrophy in Japan. Muscle & nerve\| PubMed ID: 26910583	2016
Serum Osteopontin as a Novel Biomarker for Muscle Regeneration in Duchenne Muscular Dystrophy. The American journal of pathology\| PubMed ID: 26963343	2016
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. Journal of human genetics\| PubMed ID: 27009627	2016
Utility of Cystatin C for Estimating Glomerular Filtration Rate in Patients With Muscular Dystrophy. International heart journal\| PubMed ID: 27170475	2016