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Characterization of Zebrafish Models of Marinesco-Sjögren Syndrome

PloS one, 2016-10, Vol.11 (10), p.e0165563-e0165563

2016

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Cerebral Infarction and Myalgia in a 75-year-old Man with Eosinophilic Granulomatosis with Polyangiitis

Internal Medicine, 2020/12/01, Vol.59(23), pp.3089-3092

2020

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Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice

PloS one, 2019-08, Vol.14 (8), p.e0221512

2019

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Toward the development of a vibrant, super‐aged society: The future of medicine and society in Japan

Geriatrics & gerontology international, 2021-08, Vol.21 (8), p.601-613

2021

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Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients

Orphanet journal of rare diseases, 2015-05, Vol.10 (1), p.61-61, Article 61

2015

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Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

Orphanet journal of rare diseases, 2017-08, Vol.12 (1), p.149-149, Article 149

2017

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Nuclear envelope myopathy

Neurology and clinical neuroscience, 2022-11, Vol.10 (6), p.298-303

Hayashi, Yukiko K.

2022

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Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy

Neurology, 2020-06, Vol.94 (23), p.e2441

2020

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Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1

Nature (London), 2010-04, Vol.464 (7293), p.1313-1319

2010

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A new clinicopathological entity of IgG4-related autoimmune disease

Journal of gastroenterology, 2003-10, Vol.38 (10), p.982-984

2003

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Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation

The journal of physiological sciences, 2023-11, Vol.73 (1), p.27-27, Article 27

2023

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Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

Nature medicine, 2009-06, Vol.15 (6), p.690-695

2009

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Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channels

Human molecular genetics, 2015-02, Vol.24 (3), p.637-648

2015

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A estrutura da Ética da Compaixão de Schopenhauer em relação à Filosofia Transcendental

Revista de filosofia Aurora = Journal of philosophy Aurora, 2018-04, Vol.30 (49)

Hayashi, Yukiko

2018

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Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy

The Journal of clinical investigation, 2009-09, Vol.119 (9), p.2623-2633

2009

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Characteristics of nuclear architectural abnormalities of myotubes differentiated from LmnaH222P/H222P skeletal muscle cells

In vitro cellular & developmental biology. Animal, 2024-08, Vol.60 (7), p.781-792

2024

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Hepatitis C virus infection in inclusion body myositis: A case-control study

Neurology, 2016-01, Vol.86 (3), p.211-217

2016

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Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies

Journal of neuroimmunology, 2014-09, Vol.274 (1), p.202-208

2014

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TMEM43 mutations in emery-dreifuss muscular dystrophy-related myopathy

Annals of neurology, 2011-06, Vol.69 (6), p.1005-1013

2011

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Sodium methoxide: a simple but highly efficient catalyst for the direct amidation of esters

Chemical communications (Cambridge, England), 2012-01, Vol.48 (44), p.5434-5436

2012

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A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

American journal of human genetics, 2011-06, Vol.88 (6), p.845-851

2011

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Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)

Human molecular genetics, 2007-03, Vol.16 (6), p.618-629

2007

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Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice

Skeletal muscle, 2017-10, Vol.7 (1), p.23-23, Article 23

2017

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Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice

Brain (London, England : 1878), 2014-10, Vol.137 (Pt 10), p.2670-2679

2014

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DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan

Neurology, 2015-01, Vol.84 (3), p.273-279

2015

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Characterization of Zebrafish Models of Marinesco-Sjögren Syndrome

Cerebral Infarction and Myalgia in a 75-year-old Man with Eosinophilic Granulomatosis with Polyangiitis

Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice

Toward the development of a vibrant, super‐aged society: The future of medicine and society in Japan

Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

Nuclear envelope myopathy

Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy

Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1

A new clinicopathological entity of IgG4-related autoimmune disease

Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation

Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channels

A estrutura da Ética da Compaixão de Schopenhauer em relação à Filosofia Transcendental

Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy

Characteristics of nuclear architectural abnormalities of myotubes differentiated from LmnaH222P/H222P skeletal muscle cells

Hepatitis C virus infection in inclusion body myositis: A case-control study

Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies

TMEM43 mutations in emery-dreifuss muscular dystrophy-related myopathy

Sodium methoxide: a simple but highly efficient catalyst for the direct amidation of esters

A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)

Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice

Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice

DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan

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