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Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy

Biochemical and biophysical research communications, 2007-05, Vol.357 (1), p.162-167

2007

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Structural Analysis of the Titin Gene in Hypertrophic Cardiomyopathy: Identification of a Novel Disease Gene

Biochemical and biophysical research communications, 1999-08, Vol.262 (2), p.411-417

1999

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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

Journal of the American College of Cardiology, 2004-12, Vol.44 (11), p.2192-2201

2004

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Titin Mutations as the Molecular Basis for Dilated Cardiomyopathy

Biochemical and biophysical research communications, 2002-02, Vol.291 (2), p.385-393

2002

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Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Human molecular genetics, 2012-05, Vol.21 (9), p.2039-2053

2012

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Polymorphisms in the SOD2 and HLA-DRB1 Genes Are Associated with Nonfamilial Idiopathic Dilated Cardiomyopathy in Japanese

Biochemical and biophysical research communications, 1999-08, Vol.261 (2), p.332-339

1999

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Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

Nature genetics, 1997-08, Vol.16 (4), p.379-382

1997

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Molecular etiology of idiopathic cardiomyopathy in Asian populations

Journal of cardiology, 2001, Vol.37 Suppl 1, p.139-146

2001

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Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy

Human genetics, 2000-11, Vol.107 (5), p.440-451

2000

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Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy

The American heart journal, 2001-02, Vol.141 (2), p.184-189

2001

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Clinical expression in patients with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutation / response

Circulation (New York, N.Y.), 1999-07, Vol.100 (4), p.448

1999

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MICA gene polymorphism in Takayasu's arteritis and Buerger's disease

International journal of cardiology, 1998-10, Vol.66, p.S107-S113

1998

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Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

The American journal of cardiology, 1998-12, Vol.82 (12), p.1509-1513

1998

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Clinical Expression in Patients With Hypertrophic Cardiomyopathy Caused by Cardiac Myosin-Binding Protein C Gene Mutation

Circulation (New York, N.Y.), 1999-07, Vol.100 (4), p.446-449

1999

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HLA linked with leprosy in southern China: HLA-linked resistance alleles to leprosy

International journal of leprosy and other mycobacterial diseases, 1999-12, Vol.67 (4), p.403

1999

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Hypertrophic obstructive cardiomyopathy due to a novel T-to-A transition at codon 624 in the β-myosin heavy chain (β-MHC) gene possibly related to the sudden death

International journal of cardiology, 1997-12, Vol.62 (3), p.203-209

1997

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Somatic mutations leading to incomplete extinction of HLA class I were associated with replication error phenotype-positive colorectal carcinoma

Major histocompatibility complex (Tokyo, Japan), 2007, Vol.13 (3), p.187-197

2007

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Astaxanthin affects oxidative stress and hyposalivation in aging mice

Journal of Clinical Biochemistry and Nutrition, 2016, Vol.59(2), pp.79-85

2016

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Relationships between dry mouth and oxidative stress in the elderly: A pilot study for identifying risk factors

ORAL THERAPEUTICS AND PHARMACOLOGY, 2012/04/01, Vol.31(1), pp.6-12

2012

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高齢者における口腔乾燥と酸化ストレスの関連: リスクファクター抽出のためのパイロットスタディ

歯科薬物療法, 2012/04/01, Vol.31(1), pp.6-12

2012

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Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy

Structural Analysis of the Titin Gene in Hypertrophic Cardiomyopathy: Identification of a Novel Disease Gene

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

Titin Mutations as the Molecular Basis for Dilated Cardiomyopathy

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Polymorphisms in the SOD2 and HLA-DRB1 Genes Are Associated with Nonfamilial Idiopathic Dilated Cardiomyopathy in Japanese

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

Molecular etiology of idiopathic cardiomyopathy in Asian populations

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy

Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy

Clinical expression in patients with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutation / response

MICA gene polymorphism in Takayasu's arteritis and Buerger's disease

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

Clinical Expression in Patients With Hypertrophic Cardiomyopathy Caused by Cardiac Myosin-Binding Protein C Gene Mutation

HLA linked with leprosy in southern China: HLA-linked resistance alleles to leprosy

Hypertrophic obstructive cardiomyopathy due to a novel T-to-A transition at codon 624 in the β-myosin heavy chain (β-MHC) gene possibly related to the sudden death

Somatic mutations leading to incomplete extinction of HLA class I were associated with replication error phenotype-positive colorectal carcinoma

Astaxanthin affects oxidative stress and hyposalivation in aging mice

Relationships between dry mouth and oxidative stress in the elderly: A pilot study for identifying risk factors

高齢者における口腔乾燥と酸化ストレスの関連: リスクファクター抽出のためのパイロットスタディ

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