K. Matsumura

发表

Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin

M. Matsuo, N. Tachi, K. Ohya, 1997, Neurology.

Abnormal expression of heparan sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency

K. Matsumura, M. Nakagawa, M. Osame, 1995, Neuromuscular Disorders.

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin.

I. Kanazawa, S. Kusunoki, K. Matsumura, 1997, The Journal of biological chemistry.

Detection of O-mannosyl glycans in rabbit skeletal muscle α-dystroglycan

K. Matsumura, A. Kobata, T. Endo, 1998 .

Characterization of parkin in bovine peripheral nerve

Y. Sunada, K. Matsumura, Teruo Shimizu, 2002, Brain Research.

Differential expression of the parkin gene in the human brain and peripheral leukocytes

Y. Sunada, K. Matsumura, F. Saito, 1998, Neuroscience Letters.

Structures of Sialylated O-Linked Oligosaccharides of Bovine Peripheral Nerve α-Dystroglycan

I. Kanazawa, S. Kusunoki, K. Matsumura, 1997, The Journal of Biological Chemistry.

[Congenital muscular dystrophy and alpha-dystroglycanopathy].

K. Matsumura, F. Saito, H. Hagiwara, 2008, Rinsho shinkeigaku = Clinical neurology.

A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

K. Matsumura, F. Saito, H. Tomimitsu, 2004, Neuromuscular Disorders.

Visual evoked potentials and neopterin : biop-terin ratios in urine show a high correlation in Alzheimer ' s disease

K. Matsumura, Tomoyuki IKARIt, K. Jitsukawa, 2022 .

Characterization of glial cell line‐derived neurotrophic factor family receptor α‐1 in peripheral nerve Schwann cells

K. Matsumura, F. Saito, Teruo Shimizu, 2005, Journal of neurochemistry.

Histone deacetylase inhibitor trichostatin A enhances myogenesis by coordinating muscle regulatory factors and myogenic repressors.

K. Matsumura, T. Masaki, F. Saito, 2011, Biochemical and biophysical research communications.

Motor dominant neuropathy and IgM paraproteinemia: the IgM M-protein binds to specific gangliosides

S. Kusunoki, K. Matsumura, K. Maemura, 1989, Journal of Neuroimmunology.

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity.

Y. Sunada, K. Matsumura, S. Arata, 2001, Human molecular genetics.

Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells.

J. Sahel, K. Matsumura, T. Claudepierre, 2000, Journal of cell science.

Abnormality of the Myocardial Sympathetic Nervous System in a Patient with Becker Muscular Dystrophy Detected with Iodine-123 Metaiodobenzylguanidine Scintigraphy

K. Matsumura, Teruo Shimizu, 2001, Clinical nuclear medicine.

Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.

K. Campbell, I. Nonaka, F. Leturcq, 1993, American journal of human genetics.

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

J. Ervasti, K. Campbell, S. D. Kahl, 1992, Nature.

Dense immunostainings on both neuromuscular and myotendon junctions with an anti-dystrophin monoclonal anfibody

Y. Sunada, K. Matsumura, T. Mannen, 1989 .

Secretion of laminin α2 chain in cerebrospinal fluid

K. Matsumura, Teruo Shimizu, H. Hori, 1995 .

Membranous glomerulonephritis and Grover disease with diverse neurological abnormalities ; an immunological disorder due to poliovirus infection ?

K. Matsumura, 2022 .

Defective glycosylation of α-dystroglycan contributes to podocyte flattening.

H. Kawachi, K. Matsumura, T. Toda, 2011, Kidney international.

Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscle

Y. Sunada, K. Matsumura, I. Higuchi, 2002, Neuromuscular Disorders.

Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin.

M. Matsuo, N. Tachi, S. Chiba, 2001, Pediatric neurology.

Characterization of the Transmembrane Molecular Architecture of the Dystroglycan Complex in Schwann Cells*

Y. Sunada, K. Matsumura, T. Masaki, 1999, The Journal of Biological Chemistry.

A Role of Dystroglycan in Schwannoma Cell Adhesion to Laminin*

K. Campbell, K. Matsumura, A. Kobata, 1997, The Journal of Biological Chemistry.

Tubular aggregate myopathy caused by a novel mutation in the cytoplasmic domain of STIM1

S. Tsuji, M. Sonoo, K. Matsumura, 2016, Neuromuscular Disorders.

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

I. Kanazawa, Yusuke Nakamura, I. Nonaka, 1998, Nature.

Expression of dystroglycan and laminin-2 in peripheral nerve under axonal degeneration and regeneration

Y. Sunada, K. Matsumura, T. Masaki, 2000, Acta Neuropathologica.

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

Y. Sunada, K. Matsumura, F. Saito, 1997, Neuromuscular Disorders.

A 21-kDa surface protein of Mycobacterium leprae binds peripheral nerve laminin-2 and mediates Schwann cell invasion.

V. Fischetti, K. Matsumura, Y. Shimoji, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycan complex.

K. Matsumura, F. Saito, R. Maekawa, 2001, Human molecular genetics.

Immunochemical study of connectin (titin) in neuromuscular diseases using a monoclonal antibody: connectin is degraded extensively in Duchenne muscular dystrophy

I. Nonaka, K. Matsumura, T. Mannen, 1989, Journal of the Neurological Sciences.

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve

K. Campbell, K. Matsumura, Teruo Shimizu, 1994, FEBS letters.

Protron spin‐lattice relaxation time of duchenne dystrophy skeletal muscle by magnetic resonance imaging

Y. Tateno, H. Ikehira, K. Matsumura, 1988, Muscle & nerve.

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

M. Goddeeris, K. Campbell, K. Matsumura, 2013, Nature.

Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle

K. Campbell, R. Turk, K. Matsumura, 2016, Proceedings of the National Academy of Sciences.

Overexpression of LARGE suppresses muscle regeneration via down-regulation of insulin-like growth factor 1 and aggravates muscular dystrophy in mice.

M. Sonoo, K. Matsumura, Y. Katanosaka, 2014, Human molecular genetics.

Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach

M. Sonoo, H. Kurahashi, K. Matsumura, 2020, Molecular therapy. Methods & clinical development.

Partial deficiency of dystrophin‐associated proteins in a young girl with sporadic myopathy and normal karyotype

K. Campbell, I. Nonaka, K. Matsumura, 1993, Neurology.

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12.

J. Beckmann, J. Weissenbach, A. Vignal, 1993, Human molecular genetics.

Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity

K. Campbell, J. Faulkner, N. M. Cole, 1993, Nature.

Duchenne muscular dystrophy

J. Towbin, S. W. Sernett, K. Campbell, 1993, Neurology.

Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.

J. Ervasti, K. Campbell, N. Romero, 1993, The Journal of clinical investigation.

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Yusuke Nakamura, T. Fujikado, Y. Sunada, 2003, Human molecular genetics.

Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation

K. Campbell, Y. Hara, J. Harty, 2019, Proceedings of the National Academy of Sciences.

Characterization of the protease activity that cleaves the extracellular domain of beta-dystroglycan.

K. Matsumura, Yuko Saito, F. Saito, 2006, Biochemical and biophysical research communications.

Peripheral nerve dystroglycan : its function and potential role in the molecular pathogenesis of neuromuscular diseases

K. Campbell, K. Matsumura, Teruo Shimizu, 2006 .

Disruption of dystroglycan axis by β-dystroglycan processing in cardiomyopathic hamster muscle

K. Matsumura, F. Saito, R. Maekawa, 2003, Neuromuscular Disorders.

Matrix Metalloproteinase Activity that Disrupts the Dystroglycan Complex : Its Role in the Molecular Pathogenesis of Muscular Dystrophies

K. Matsumura, F. Saito, R. Maekawa, 2003 .

The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation.

Y. Sunada, K. Matsumura, F. Saito, 1997, Histology and histopathology.

Dystroglycan Is a Dual Receptor for Agrin and Laminin-2 in Schwann Cell Membrane*

M. Ruegg, K. Matsumura, L. Anderson, 1996, The Journal of Biological Chemistry.

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

K. Campbell, J. Kaplan, K. Matsumura, 1992, Nature.

Dystrophin–glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophies

K. Campbell, K. Matsumura, 1994, Muscle & nerve.

J. Ervasti, C. Leveille, K. Campbell, 1991, Neuron.

Topographic pattern of the rearrangement of the dystrophin gene in Japanese Duchenne muscular dystrophy

T. Arinami, H. Yamada, K. Matsumura, 1993, Human Genetics.

Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy

K. Campbell, V. Dubowitz, K. Matsumura, 1994, Neuromuscular Disorders.

Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two South Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy

K. Campbell, V. Dubowitz, K. Matsumura, 1994, Neuromuscular Disorders.

Purification of dystrophin‐related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells

K. Campbell, K. Matsumura, Douglas M. Shasby, 1993, FEBS letters.

Differential expression of dystrophin, utrophin and dystrophin‐associated proteins in peripheral nerve

K. Campbell, K. Matsumura, Teruo Shimizu, 1993, FEBS letters.

Secretion of N-terminal domain of α-dystroglycan in cerebrospinal fluid.

K. Matsumura, T. Masaki, F. Saito, 2011, Biochemical and biophysical research communications.

Processing and secretion of the N‐terminal domain of α‐dystroglycan in cell culture media

K. Matsumura, F. Saito, Teruo Shimizu, 2008, FEBS letters.

Defective peripheral nerve myelination and neuromuscular junction formation in fukutin‐deficient chimeric mice

K. Matsumura, T. Toda, Yuko Saito, 2007, Journal of neurochemistry.

Aberrant glycosylation of α‐dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy

K. Campbell, M. Blank, K. Matsumura, 2005, FEBS letters.

Biological Role of Dystroglycan in Schwann Cell Function and Its Implications in Peripheral Nervous System Diseases

K. Matsumura, T. Masaki, 2010, Journal of biomedicine & biotechnology.

Association of dystroglycan and laminin-2 coexpression with myelinogenesis in peripheral nerves

K. Matsumura, S. Higuchi, T. Masaki, 2003, Medical Electron Microscopy.

Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro

S. Takeda, K. Matsumura, A. Kudo, 2009, Mechanisms of Development.

Fukuyama-type congenital muscular dystrophy and defective glycosylation of α-dystroglycan

K. Matsumura, F. Saito, 2011, Skeletal Muscle.

Fukuyama‐type congenital muscular dystrophy (FCMD) and α‐dystroglycanopathy

Y. Sunada, H. Kurahashi, T. Terashima, 2003 .

Fukuyama-type Congenital Muscular Dystrophy and Abnormal Glycosylation of α-Dystroglycan

Y. Sunada, H. Kurahashi, T. Terashima, 2003 .

Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.

F. Leturcq, J. Kaplan, L. Morandi, 1994, The Journal of clinical investigation.

Restoration of dystrophin‐associated proteins in skeletal muscle of mdx mice transgenic for dystrophin gene

K. Campbell, C. Caskey, Cheng Chi Lee, 1993, FEBS letters.

Deficiency of dystrophin-associated proteins: A common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies

K. Campbell, K. Matsumura, 1993, Neuromuscular Disorders.

Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study

K. Campbell, K. Matsumura, M. Chevallay, 1994, Neuromuscular Disorders.

Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy

K. Campbell, M. Passos-Bueno, M. Zatz, 1994, Journal of the Neurological Sciences.

Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy

K. Campbell, F. Leturcq, J. Kaplan, 1994, Neuromuscular Disorders.

The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies

K. Campbell, I. Nonaka, J. Kaplan, 1993, Neuromuscular Disorders.

A Japanese Family With Two Types of Muscular Dystrophy: DNA Analysis and the Dystrophin Test

K. Matsumura, Teruo Shimizu, T. Toda, 1991, Journal of child neurology.

Degradation of connectin (titin) in Fukuyama type congenital muscular dystrophy: immunochemical study with monoclonal antibodies

Y. Sunada, I. Nonaka, K. Matsumura, 1990, Journal of the Neurological Sciences.

Characterization of Dystroglycan‐Laminin Interaction in Peripheral Nerve

I. Kanazawa, K. Campbell, K. Matsumura, 1996, Journal of neurochemistry.

Expression of Dystroglycan and the Laminin-α2 Chain in the Rat Peripheral Nerve during Development

K. Matsumura, A. Hirata, T. Masaki, 2002, Experimental Neurology.

Expression of dystroglycan complex in satellite cells of dorsal root ganglia

K. Matsumura, A. Hirata, T. Masaki, 2001, Acta Neuropathologica.

A monoclonal antibody against a synthetic polypeptide fragment of dystrophin (amino acid sequence from position 215 to 264).

I. Nonaka, K. Matsumura, T. Mannen, 1988 .

N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

K. Campbell, K. Matsumura, Mary E. Anderson, 2023, eLife.

Characterization of a 30-kDa Peripheral Nerve Glycoprotein That Binds Laminin and Heparin*

Y. Sunada, K. Matsumura, Teruo Shimizu, 1997, The Journal of Biological Chemistry.

Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.

K. Campbell, F. Leturcq, J. Kaplan, 1993, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Primary Non‐Hodgkin Lymphoma of the Skull Base Presenting with Garcin Syndrome: MRI Manifestations

K. Matsumura, K. Toyoda, Teruo Shimizu, 2009, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

AN IMMUNOLOGICAL HOMOLOGY BETWEEN NEUROFILAMENT AND MUSCLE ELASTIC EILAMENT: A MONOCLONAL ANTIBODY CROSS-REACTS WITH NEUROFILAMENT SUBUNITS AND CONNECTIN

K. Matsumura, K. Maruyama, T. Mannen, 1988 .

Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?

Y. Sunada, K. Matsumura, F. Saito, 1999, Cellular and molecular biology.

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

K. Campbell, I. Nonaka, K. Matsumura, 1993, The Lancet.

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Y. Sunada, H. Kurahashi, T. Terashima, 2003, Congenital anomalies.

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.

T. Fujiwara, K. Matsumura, T. Mitsui, 1995, The Journal of clinical investigation.

Anterograde amnesia associated with infarction of the anterior fornix and genu of the corpus callosum.

K. Matsumura, Yuko Saito, Teruo Shimizu, 2006, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Duchenne muscular dystrophy carriers

Y. Tateno, H. Ikehira, K. Matsumura, 1989, Neuroradiology.

Proteolysis of β-dystroglycan in muscular diseases

I. Nishino, K. Matsumura, I. Higuchi, 2005, Neuromuscular Disorders.