Nakura Jun | Department Of Geriatric Medicine Ehime University Graduate School Of Medicine

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著作論文

Accumulation of common polymorphisms is associated with development of hypertension : a 12-year follow-up from the Ohasama study
Asymptomatic Cerebral Microbleeds Seen in Healthy Subjects Have a Strong Association With Asymptomatic Lacunar Infarction(Stroke)
17-Year Follow-up Study of a Patient With Obstructive Hypertrophic Cardiomyopathy With a Deletion Mutation in the Cardiac Myosin Binding Protein C Gene
Association of Genetic Polymorphisms of Endothelin-Converting Enzyme-1 Gene with Hypertension in a Japanese Population and Rare Missense Mutation in Preproendothelin-1 in Japanese Hypertensives
Association of Angiotensin II Type 2 Receptor Gene Variant with Hypertension
Identification of Hypertension-Susceptibility Genes and Pathways by a Systemic Multiple Candidate Gene Approach : The Millennium Genome Project for Hypertension
Genome-Wide Linkage Disequilibrium Mapping of Hypertension in Japan
Association of the GNAS1 Gene Variant with Hypertension Is Dependent on Alcohol Consumption
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D8S1223 LOCUS
TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1444 AND D8S1445 LOCI
TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1218 AND D8S1219 LOCI
A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT AT THE D8S1222 LOCUS
THREE DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1217, D8S1220, AND D8S1221 LOCI
TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1442 AND D8S1443 LOCI
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D8S1054
Endothelial Nitric Oxide Synthase Polymorphism (Glu298Asp) on Cardiovascular Events for Patients with Hypertrophic Cardiomyopathy(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Societ
Association of Monocyte Chemoattractant Protein 1 (MCP-1) Gene Polymorphism With Susceptibility to Dilated Cardiomyopathy
Relation Between Angiotensin-Converting Enzyme II Genotype and Atrial Fibrillation in Japanese Patients With Hypertrophic Cardiomyopathy
Polymorphisms in Vitamin K-Dependent γ-Carboxylation-Related Genes Influence Interindividual Variability in Plasma Protein C and Protein S Activities in the General Population
Genetic Variations of HSD11B2 in Hypertensive Patients and in the General Population, Six Rare Missense/Frameshift Mutations
A Novel Missense Mutation, F826Y, in the Mineralocorticoid Receptor Gene in Japanese Hypertensives : Its Implications for Clinical Phenotypes
OJ-224 Effect of the GNB3 Gene Variant on Cardiovascular Events in Patients with Idiopathic Dilated Cardiomyopathy(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
Migraine Is Associated with Enhanced Arterial Stiffness
Interaction between Serotonin 2A Receptor and Endothelin-1 Variants in Association with Hypertension in Japanese
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
Plasma Hepatocyte Growth Factor and the Relationship between Risk Factor and Carotid Atherosclerosis
Genotype-Specific Association between Circulating Soluble Cellular Adhesion Molecules and Carotid Intima-Media Thickness in Community Residents : J-SHIPP Study
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
Deletion Polymorphism of ACE Gene Is Associated with Higher Blood Pressure after Hospitalization in Normotensive Subjects
The Genes Responsible for Human Progeroid Syndromes
Effect of Genetic Polymorphism of OATP-C (SLCO1B1) on Lipid-Lowering Response to HMG-CoA Reductase Inhibitors
Association of Dopamine β-Hydroxylase Polymorphism with Hypertension through Interaction with Fasting Plasma Glucose in Japanese
Association of a GNAS1 Gene Variant with Hypertension and Diabetes Mellitus
FRS-082 Endothelial Nitric Oxide Synthase Gene Polymorphism (Glu298Asp) in Patients with Coexistent Hypertrophic Cardiomyopathy and Coronary Vasospasm(NO and Cardiovascular System (H) : FRS10)(Featured Research Session (English))
Effect of time standing up on orthostatic blood pressure change in the elderly : The J-SHIPP Study
Microalbuminuria and Arterial Stiffness in a General Population : the Shimanami Health Promoting Program (J-SHIPP) Study
Angiotensin-Converting Enzyme Gene Deletion Allele Disappear Brachial-Carotid Pulse Pressure Amplification
The-4,752 C/T Polymorphism in the Presenilin 1 Gene Increases the Risk of Alzheimer's Disease in Apolipoprotein E4 Carriers
The-4,752 C/T Polymorphism in the Presenilin 1 Gene Increases the Risk of Alzheimer's Disease in Apolipoprotein E4 Carriers
Hunting for genes for hypertension : the Millennium Genome Project for Hypertension

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