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High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project

Human molecular genetics, 2008-02, Vol.17 (4), p.617-627

2008

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Association of ACE I/D polymorphism with cardiovascular risk factors

Human genetics, 2000-09, Vol.107 (3), p.239-242

2000

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Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathy

Journal of human genetics, 2002-04, Vol.47 (4), p.184-189

2002

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Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin system

Journal of human genetics, 2001-01, Vol.46 (5), p.278-284

2001

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Helicases and aging

Cellular and molecular life sciences : CMLS, 2000-05, Vol.57 (5), p.716-730

2000

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Association Analysis of a Polymorphism of the Angiotensin Converting Enzyme Gene with Essential Hypertension in the Japanese Population

Biochemical and biophysical research communications, 1993-03, Vol.191 (2), p.399-404

1993

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Positional Cloning of the Werner's Syndrome Gene

Science (American Association for the Advancement of Science), 1996-04, Vol.272 (5259), p.258-262

1996

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Microalbuminuria and Arterial Stiffness in a General Population: the Shimanami Health Promoting Program (J-SHIPP) Study

Hypertension Research, 2004, Vol.27(7), pp.471-477

2004

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Molecular Genetic Analysis of Werner Syndrome

Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics, 2001/11/25, Vol.38(6), pp.766-768

Nakura, Jun

2001

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Association of Endothelin-1 Gene Variant With Hypertension

Hypertension (Dallas, Tex. 1979), 2003-01, Vol.41 (1), p.163-167

2003

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Polymorphism of the Monocyte Chemoattractant Protein (MCP-1) Gene Is Associated with the Plasma Level of MCP-1 But Not with Carotid Intima-Media Thickness

Hypertension Research, 2003, Vol.26(9), pp.677-683

2003

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Homozygosity Mapping of the Werner Syndrome Locus (WRN)

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.600-608

1994

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Toward localization of the werner syndrome gene by linkage disequilibrium and ancestral haplotyping : Lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers

American journal of human genetics, 1996-06, Vol.58 (6), p.1286-1302

1996

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Orthostatic Systolic Hypotension and the Reflection Pressure Wave

Hypertension research, 2005-06, Vol.28 (6), p.537-543

2005

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Homozygosity mapping and Werner's syndrome

The Lancet (British edition), 1992-04, Vol.339 (8799), p.1002-1002

1992

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Symptomatic cerebral infarction and ACE I/D polymorphism in japanese patients: comparison with asymptomatic cerebral infarction

American journal of hypertension, 2000-04, Vol.13 (4), p.5A-5A

2000

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D006: Carotid atherosclerosis and gene polymorphisms of renin angiotensin system in elderly subject in sekizen, japan

American journal of hypertension, 2000-04, Vol.13 (S2), p.74A-75A

2000

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B006: Orthostatic hypertension is associated with carotid atherosclerosis: sekizen study, japan

American journal of hypertension, 2000-04, Vol.13 (S2), p.188A-188A

2000

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C013: Post prandial hypotension evaluated by 24-hour blood pressure monitoring

American journal of hypertension, 2000-04, Vol.13 (S2), p.214A-214A

2000

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D005: Genetic predisposition of orthostatic dysregulation of blood pressure in the elderly in sekizen, japan

American journal of hypertension, 2000-04, Vol.13 (S2), p.74A-74A

2000

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Association of Angiotensin II Type 2 Receptor Gene Variant with Hypertension

Hypertension Research, 2003, Vol.26(7), pp.547-552

2003

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Premature aging: recent advances

No To Shinkei, 1998-11, Vol.50 (11), p.977

1998

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Association of GNB3 gene with pulse pressure and clustering of risk factors for cardiovascular disease in Japanese

Biochemical and biophysical research communications, 2004-04, Vol.316 (3), p.744-748

2004

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Association of GNAS1 Gene Variant With Hypertension Depending on Smoking Status

Hypertension (Dallas, Tex. 1979), 2002-09, Vol.40 (3), p.261-265

2002

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Mutations in the consensus helicase domains of the Werner syndrome gene

American journal of human genetics, 1997-02, Vol.60 (2), p.330-341

1997

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High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project

Association of ACE I/D polymorphism with cardiovascular risk factors

Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathy

Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin system

Helicases and aging

Association Analysis of a Polymorphism of the Angiotensin Converting Enzyme Gene with Essential Hypertension in the Japanese Population

Positional Cloning of the Werner's Syndrome Gene

Microalbuminuria and Arterial Stiffness in a General Population: the Shimanami Health Promoting Program (J-SHIPP) Study

Molecular Genetic Analysis of Werner Syndrome

Association of Endothelin-1 Gene Variant With Hypertension

Polymorphism of the Monocyte Chemoattractant Protein (MCP-1) Gene Is Associated with the Plasma Level of MCP-1 But Not with Carotid Intima-Media Thickness

Homozygosity Mapping of the Werner Syndrome Locus (WRN)

Toward localization of the werner syndrome gene by linkage disequilibrium and ancestral haplotyping : Lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers

Orthostatic Systolic Hypotension and the Reflection Pressure Wave

Homozygosity mapping and Werner's syndrome

Symptomatic cerebral infarction and ACE I/D polymorphism in japanese patients: comparison with asymptomatic cerebral infarction

D006: Carotid atherosclerosis and gene polymorphisms of renin angiotensin system in elderly subject in sekizen, japan

B006: Orthostatic hypertension is associated with carotid atherosclerosis: sekizen study, japan

C013: Post prandial hypotension evaluated by 24-hour blood pressure monitoring

D005: Genetic predisposition of orthostatic dysregulation of blood pressure in the elderly in sekizen, japan

Association of Angiotensin II Type 2 Receptor Gene Variant with Hypertension

Premature aging: recent advances

Association of GNB3 gene with pulse pressure and clustering of risk factors for cardiovascular disease in Japanese

Association of GNAS1 Gene Variant With Hypertension Depending on Smoking Status

Mutations in the consensus helicase domains of the Werner syndrome gene

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