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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Nature genetics, 1998-09, Vol.20 (1), p.31-36

1998

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Interaction between Emerin and Nuclear Lamins

Journal of biochemistry (Tokyo), 2001-02, Vol.129 (2), p.321-327

2001

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Mutations in the integrin α7 gene cause congenital myopathy

Nature genetics, 1998-05, Vol.19 (1), p.94-97

1998

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Laminin α2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy

FEBS letters, 1997-09, Vol.415 (1), p.33-39

1997

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Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya

The European journal of neuroscience, 2007-04, Vol.25 (7), p.2009-2020

2007

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MKBP, a Novel Member of the Small Heat Shock Protein Family, Binds and Activates the Myotonic Dystrophy Protein Kinase

The Journal of cell biology, 1998-03, Vol.140 (5), p.1113-1124

1998

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Muscular dystrophy

Neuropathology, 2000-09, Vol.20 (s1), p.34-41

Arahata, Kiichi

2000

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Prominent expression of glial cell line-derived neurotrophic factor in human skeletal muscle

Journal of comparative neurology (1911), 1998-12, Vol.402 (3), p.303-312

1998

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Cloning and characterization of two neural‐salient serine/arginine‐rich (NSSR) proteins involved in the regulation of alternative splicing in neurones

Genes to cells : devoted to molecular & cellular mechanisms, 1999-10, Vol.4 (10), p.593-606

1999

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Abnormal localization of laminin subunits in muscular dystrophies

Journal of the neurological sciences, 1993-10, Vol.119 (1), p.53-64

1993

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Increased expression level of the splicing variant of SIP1 in motor neuron diseases

The international journal of biochemistry & cell biology, 2002-06, Vol.34 (6), p.699-707

2002

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Analysis of inflammatory cells and complement C3 in bupivacaine-induced myonecrosis

Muscle & nerve, 1991-06, Vol.14 (6), p.515-520

1991

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Characterization of the DNA binding property of emerin

Proceedings of the Japan Academy, Series B, 2001, Vol.77(7), pp.140-143

2001

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Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients

BMC neurology, 2002-08, Vol.2 (1), p.7-7, Article 7

2002

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Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes of autoinvasive cells in polymyositis and inclusion body myositis

Annals of neurology, 1984-08, Vol.16 (2), p.209-215

1984

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Mononuclear cells in myopathies: Quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies

Human pathology, 1986-07, Vol.17 (7), p.704-721

1986

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Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell-mediated cytotoxicity and muscle fiber necrosis

Annals of neurology, 1988-02, Vol.23 (2), p.168-173

1988

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Monoclonal antibody analysis of mononuclear cells in myopathies. V: Identification and quantitation of T8+ cytotoxic and T8+ suppressor cells

Annals of neurology, 1988-05, Vol.23 (5), p.493-499

1988

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Developmental expression of myotonic dystrophy protein kinase in brain and its relevance to clinical phenotype

Acta neuropathologica, 2000-11, Vol.100 (5), p.513-520

2000

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The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Human molecular genetics, 2001-08, Vol.10 (17), p.1761-1766

2001

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Monoclonal antibody analysis of mononuclear cells in myopathies. III: Immunoelectron microscopy aspects of cell-mediated muscle fiber injury

Annals of neurology, 1986-02, Vol.19 (2), p.112-125

1986

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Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseases

Neuroscience letters, 1998-12, Vol.257 (3), p.165-167

1998

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Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy

The New England journal of medicine, 1989-01, Vol.320 (3), p.138-142

1989

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Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy

Neurology, 1998-06, Vol.50 (6), p.1791-1794

1998

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Emerin and cardiomyopathy in Emery–Dreifuss muscular dystrophy1This paper was presented at the 3rd Congress of the World Muscle Society (WMS) in Naples, Italy, May 29–30 1998.1

Neuromuscular disorders : NMD, 1999-03, Vol.9 (2), p.108-114

1999

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Interaction between Emerin and Nuclear Lamins

Mutations in the integrin α7 gene cause congenital myopathy

Laminin α2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy

Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya

MKBP, a Novel Member of the Small Heat Shock Protein Family, Binds and Activates the Myotonic Dystrophy Protein Kinase

Muscular dystrophy

Prominent expression of glial cell line-derived neurotrophic factor in human skeletal muscle

Cloning and characterization of two neural‐salient serine/arginine‐rich (NSSR) proteins involved in the regulation of alternative splicing in neurones

Abnormal localization of laminin subunits in muscular dystrophies

Increased expression level of the splicing variant of SIP1 in motor neuron diseases

Analysis of inflammatory cells and complement C3 in bupivacaine-induced myonecrosis

Characterization of the DNA binding property of emerin

Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients

Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes of autoinvasive cells in polymyositis and inclusion body myositis

Mononuclear cells in myopathies: Quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies

Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell-mediated cytotoxicity and muscle fiber necrosis

Monoclonal antibody analysis of mononuclear cells in myopathies. V: Identification and quantitation of T8+ cytotoxic and T8+ suppressor cells

Developmental expression of myotonic dystrophy protein kinase in brain and its relevance to clinical phenotype

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Monoclonal antibody analysis of mononuclear cells in myopathies. III: Immunoelectron microscopy aspects of cell-mediated muscle fiber injury

Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseases

Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy

Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy

Emerin and cardiomyopathy in Emery–Dreifuss muscular dystrophy1This paper was presented at the 3rd Congress of the World Muscle Society (WMS) in Naples, Italy, May 29–30 1998.1

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