PJ-689 Relationship between a Metabolic Syndrome and the Polymorphism of the Beta3 Adrenergic Receptor Gene in a General Sample (S-town study)(Diabetes/Obesity/Metabolic syndrome-13 (H) PJ116,Poster Session (Japanese),The 70th Anniversary Annual Scientifi
スポンサーリンク
概要
- 論文の詳細を見る
- 社団法人日本循環器学会の論文
- 2006-03-01
著者
-
TABARA Yasuharu
Department of Basic Medical Research and Education, Ehime University Graduate School of Medicine
-
HORIE Minoru
Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science
-
Ueshima Hirotsugu
Department of Health Science, Shiga University of Medical Science
-
Okamura Tomonori
Department of Preventive Cardiology, National Cardiovascular center
-
Kadowaki Takashi
Department of Health Science, Shiga University of Medical Science
-
Mochizuki T
Division Of Anti-aging And Genomics Ehime Proteo-medicine Research Center
-
Mochizuki T
Department Of Radiology Ehime University School Of Medicine Shitsukawa
-
Tsujita Yasuyuki
Department Of Geriatric Medicine Osaka University Graduate School Of Medicine
-
Tabara Yasuharu
国立循環器病センター研究所 疫学部
-
Tabara Yasuharu
自治医科大学 循環器内科
-
Tsubakimoto Yoshinori
Department Of Cardiolgy Kyoto Prefectural University Of Medicine
-
Tabara Yasuharu
Department Of Basic Medical Research And Education Ehime University Graduate School Of Medicine
-
TAMAKI Shinji
Division of Cardiology, Department of Medicine, Kohka Public Hospital
-
KITA Yoshikuni
Department of Health Science, Shiga University of Medical Science
-
Nakamura Yasuyuki
Division of Cardiovascular Epidemiology, Department of Living and Welfare, Faculty of Home Economics
-
Miki Tetsurou
Department of Geriatric Medicine, Ehime University School of Medicine
-
Tarutani Yasuhiro
Division Of Cardiology Department Of Medicine Kohka Public Hospital
-
Mochizuki Teruhito
Department Of Radiology Ehime University School Of Medicine Shitsukawa
-
Takishita Shuichi
ハートライフ病院 循環器科
-
Kadowaki Takashi
滋賀大学 医学部健康科学科
-
Katanosaka Yuki
国立循環器病センター
-
Tsujita Yasuyuki
Department Of Basic Medical Research And Education Ehime University Graduate School Of Medicine
-
Kadowaki Takashi
Department Of Cardiovascular Medicine Graduate School Of Medicine University Of Tokyo
-
Takagi Satoru
The Second Department Of Internal Medicine School Of Medicine Sapporo Medical University
-
Miki Tetsurou
Department Of Geriatric Medicine Ehime University School Of Medicine
-
Tamaki Shinji
Division Of Cardiology Department Of Medicine Kohka Public Hospital
-
Kita Yoshikuni
Department Of Health Science Shiga University Of Medical Science
-
Takishita Shuichi
Department Of Molecular Cardiology Osaka University Graduate School Of Medicine
-
Nakamura Yasuyuki
Heart Rhythm Center Department Of Cardiovascular Medicine Shiga University Of Medical Science
-
Saruta Takao
Fukuoka University School Of Medicine
-
Takiuchi Shin
Division Of Hypertension And Nephrology National Cardiovascular Center
-
Ueshima Hirotsugu
Department Of Health Sceicne Shiga University Of Medical Science
-
Tarutani Yasuhiro
Department Of Cardiology Kohka Public Hospital
-
Takashima Seiji
Department Of Molecular Cardiology Osaka University Graduate School Of Medicine
-
Nakamura Yasuyuki
Department Of Health Science Shiga University Of Medical Science
-
Horie Minoru
Department Of Cardiac Physiology National Cardiovascular Center Research Institute
-
Okamura Tomonori
Department Of Cardiology National Cardiovascular Center
-
Sano Toshio
2nd Department Of Internal Medicine School Of Medicine Yokohama City University
-
Takiuchi Shin
Department Of Molecular Cardiology Osaka University Graduate School Of Medicine
-
Matayoshi Tetsutaro
Division Of Hypertension And Nephrology National Cardiovascular Center
-
Tamaki Shinji
Department Of Cardiology Shiga University Of Medical Science
-
Yoshida Toshiharu
Department Of Nephrology Sendai Shakaihoken Hospital
-
Tsukamoto Yusuke
Division Of Nephrology Department Of Internal Medicine Juntendo University School Of Medicine
-
Niwa Yoshimitsu
自治医科大学 公衆衛生学
-
Takemura Yukihiro
Department Of Geriatric Medicine And Nephrology Osaka University Graduate School Of Medicine
-
Nakamura Yasuyuki
滋賀医科大学 循環器内科
-
Nakamura Yasuyuki
Division Of Cardiology Department Of Medicine Shiga University Of Medical Science
-
Kadowaki Takashi
Department Of Cardiology Kawasaki Medical School
関連論文
- Association of the Functional Variant in the 3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Gene With Low-Density Lipoprotein-Cholesterol in Japanese
- Comparison of the long-term effects of candesartan and olmesartan on plasma angiotensin II and left ventricular mass index in patients with hypertension
- A Genome-Wide Association Study of Hypertension-Related Phenotypes in a Japanese Population
- Accumulation of common polymorphisms is associated with development of hypertension : a 12-year follow-up from the Ohasama study
- Association of SLC6A9 Gene Variants with Human Essential Hypertension
- Asymptomatic Cerebral Microbleeds Seen in Healthy Subjects Have a Strong Association With Asymptomatic Lacunar Infarction(Stroke)
- FRS-031 Additional Gene Modifiers Reduce Effectiveness of β-blockers in the Long QT Type 1 Syndrome(Arrhythmia-Basic : Molecular and Genetic : Basis (A) : FRS4)(Featured Research Session (English))
- ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
- ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
- FRS-066 When and How should We Use Central BP in Clinical Hypertension? : Report from ABC-J Study(FRS14,New Aspects for Hypertension (H),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- OE-145 Multi-center Cross-sectional Study to Characterize Antihypertensive Treatments in terms of Central Blood Pressure Evaluated by Radial Artery Pulse Waveform(Hypertension, clinical(01)(H),Oral Presentation(English),The 72nd Annual Scientific Meeting
- NRSF Is Involved in Molecular Pathways for Sudden Death Associated with Heart Failure
- Hydroxyzine, a First Generation H_1-Receptor Antagonist, Inhibits Human Ether-a-go-go-Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation
- An Association between Decreased Estimated Glomerular Filtration Rate and Arterial Stiffness
- An Association between Metabolic Syndrome and the Estimated Glomerular Filtration Rate
- PJ-571 Multiple Mechanisms underlie Long QT Syndrome by the Change of Amino Acid R259 in the Intracellular S4-S5 Linker of KCNQ1(PJ096,Arrhythmia, Others (Clinical/Pathophysiology) 4 (A),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The
- PE-106 SCN5A and Lamin A/C Gene Mutations are Highly Prevalent in Patients with Familial Bradyarrhythmic Disorders(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
- Abnormal nocturnal blood pressure profile is associated with mild cognitive impairment in the elderly : the J-SHIPP study
- Serum Gamma-Glutamyl Transferase Levels are Associated with Metabolic Syndrome in Community-Dwelling Individuals
- Association of monocyte chemoattractant protein 1 gene polymorphism with susceptibility to nonfamilial idiopathic dilated cardiomyopathy
- Alcohol Consumption Is Associated with Decreased Insulin Resistance Independent of Body Mass Index in Japanese Community-Dwelling Men
- Silent cerebral microbleeds associated with arterial stiffness in an apparently healthy subject
- FRS-068 Class Differences in the Effects of BP-lowering Drugs on Central Blood Pressure : The J-SHIPP Study(FRS14,New Aspects for Hypertension (H),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Association between Serum Gamma-Glutamyl Transferase Level and Prehypertension among Community-Dwelling Men
- An Association between Body Mass Index and Estimated Glomerular Filtration Rate
- Effects of Obesity and Smoking on Mental Stress-Induced Blood Pressure and Augmentation Index Responses in Normotensive Young Males : The J-SHIPP Study
- Association of Atrial Arrhythmia and Sinus Node Dysfunction in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
- Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms
- Whole-Body Periodic Acceleration Enhances Brachial Endothelial Function
- PJ-457 Chronic Effects of Angiotensin II Receptor Blockade on Coronary Fibrinolytic Function in Patients with Coronary Artery Disease(Coronary circulation, basic/clinical-3, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-453 Effects of Chronic Smoking on Coronary Fibrinolytic Function in Women with Normal Coronary Arteries(Coronary circulation, basic/clinical-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Relationship between Metabolic Syndrome and Trp64Arg Polymorphism of the β3-Adrenergic Receptor Gene in a General Sample : The Shigaraki Study
- The Association between Morning Hypertension and Metabolic Syndrome in Hypertensive Patients
- Impact of Paraoxonase Polymorphism (Q192R) on Endothelial Function in Intact Coronary Circulation
- PJ-772 The Present Condition of the Morning Hypertension Patients after JSH2004(Hypertension, clinical-12 (H) PJ134,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-689 Relationship between a Metabolic Syndrome and the Polymorphism of the Beta3 Adrenergic Receptor Gene in a General Sample (S-town study)(Diabetes/Obesity/Metabolic syndrome-13 (H) PJ116,Poster Session (Japanese),The 70th Anniversary Annual Scientifi
- PJ-388 The Impact of Whole-body, Periodic Acceleration on Vascular Endothelial Function and Nitric Oxide Release(Exercise test/Cardiac rehabilitation-3 (IHD) PJ66,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Cir
- PJ-010 Aortic Stiffening Precedes Coronary Endothelial Dysfunction in Type II Diabetes Mellitus(Coronary circulation, basic/clinical-4 (IHD) PJ2,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-689 Relationship between a Metabolic Syndrome and the Polymorphism of the Beta3 Adrenergic Receptor Gene in a General Sample (S-town study)(Diabetes/Obesity/Metabolic syndrome-13 (H) PJ116,Poster Session (Japanese),The 70th Anniversary Annual Scientifi
- PJ-388 The Impact of Whole-body, Periodic Acceleration on Vascular Endothelial Function and Nitric Oxide Release(Exercise test/Cardiac rehabilitation-3 (IHD) PJ66,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Cir
- FRS-149 Mutation Site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in Japanese Families with Congenital LQT1 Syndrome(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- 5 Genotype- and Mutation site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in the Long QT Syndrome(APSC/JCS Joint Symposium (APSC) (H) : Emerging Issue in Cardiology for Asian)(Special Program)
- ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
- Novel Mutation of Plakophilin-2 Associated With Arrhythmogenic Right Ventricular Cardiomyopathy
- A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation
- PJ-571 Multiple Mechanisms underlie Long QT Syndrome by the Change of Amino Acid R259 in the Intracellular S4-S5 Linker of KCNQ1(PJ096,Arrhythmia, Others (Clinical/Pathophysiology) 4 (A),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The
- PE-106 SCN5A and Lamin A/C Gene Mutations are Highly Prevalent in Patients with Familial Bradyarrhythmic Disorders(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
- Combined Analysis of Polymorphisms in Angiotensinogen and Adducin Genes and Their Effects on Hypertension in a Japanese Sample : The Shigaraki Study
- Change of Medication to Candesartan is Effective for Patients with Early Morning Surge in Blood Pressure (from the ATOM Study) (Hypertension, Clinical 10 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 1 Molecular Basis for Low Penetrance in the Long QT Syndrome(Meet the Expert 7 (ME7) (A) : Issues on Sudden Cardiac Death)(Special Program)
- Molecular and Genetic Basis for the Treatment of Long QT-Related Lethal Ventricular Arrhythmias
- Verapamil binding sites of K_ channel may reside on the cytosolic end of the TM2 of the pore-forming subunit, Kir6.2
- Why does intracoronary ACh injection induce torsade de pointes in long QT syndrome? : Role of Nitric Oxide
- Therapeutic concentrations of bepridil voltage-dependently block of IK_s reconstituted by KCNQ1/KCNE1
- LQT1, but not LQT2, patients show an exercise-induced increase in transmural dispersion of repolarization (TDR)
- Association of Angiotensin II Type 2 Receptor Gene Variant with Hypertension
- Electrical Remodeling of the Ventricular Myocardium in Myocarditis : Studies of Rat Experimental Autoimmune Myocarditis
- OJ-012 Mutation Analysis for the Human Cardiac Ryanodine Receptor Gene (RyR2) in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Soci
- PE-104 Severer Phenotypes of Long QT Syndrome are Associated with Compound Mutations : A Multicenter Study(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soci
- FRS-052 Identification and Functional Characterization of a Novel Intronic Splicing Mutation in KCNQ1 Associated with Long QT Syndrome(FRS11,New Insights into Basic Mechanisms of Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientifi
- 2 Latent Genetic Backgrounds and Molecular Pathogenesis of Drug-induced Long QT Syndrome(Proarrhythmic Risk of Drugs and Their Evaluation,Symposium 7 (SY-07) (I),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- 1 A Novel Genetic Marker for Potential Risk of QT Prolongation and Cardiac Sudden Death : KCNE1-D85N Polymorphism(Biomarkers, Genetic Polymorphism, and Risk Estimation,Symposium 1 (SY-01) (H),The 73rd Annual Scientific Meeting of The Japanese Circulation
- Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up
- Mutation Analysis of the Glycerol-3 Phosphate Dehydrogenase-1 Like (GPD1L) Gene in Japanese Patients With Brugada Syndrome
- Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome
- A Novel Mutation Associated With Jervell and Lange-Nielsen Syndrome in a Japanese Family
- PE-251 Mutation analysis of the Glycerol-3 Phosphate Dehydrogenase-1 Like (GPD1L) Gene in Japanese Patients with Brugada Syndrome(Arrhythmia, diagnosis/Pathophysiology/EPS(07)(A),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese C
- OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- OE-391 Cardiac sodium channel gene mutations are prevalent in Japanese patients with familial sick sinus syndrome(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation So
- OE-276 Familial Dilated Cardiomyopathy with Conduction Disease Caused by Lamin A/C Mutations : Efficacy of the Cardiac Resynchronization Therapy with a Defibrillator(Cardiomyopathy, basic/clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientif
- FRS-109 A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation(New Horizon in Diagnosis and Pathophysiology of Arrhythmia(A),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Circulation Soci
- Identification of Hypertension-Susceptibility Genes and Pathways by a Systemic Multiple Candidate Gene Approach : The Millennium Genome Project for Hypertension
- Effect of Acute and Long-Term Aerobic Exercise on Arterial Stiffness in the Elderly
- Genome-Wide Linkage Disequilibrium Mapping of Hypertension in Japan
- Association of the GNAS1 Gene Variant with Hypertension Is Dependent on Alcohol Consumption
- A Pilot Study Suggests that the G/G Genotype of Resistin Single Nucleotide Polymorphism at -420 May Be an Independent Predictor of a Reduction in Fasting Plasma Glucose and Insulin Resistance by Pioglitazone in Type 2 Diabetes
- Association of Monocyte Chemoattractant Protein 1 (MCP-1) Gene Polymorphism With Susceptibility to Dilated Cardiomyopathy
- 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
- Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin system
- Effect of Genetic Polymorphism of OATP-C (SLCO1B1) on Lipid-Lowering Response to HMG-CoA Reductase Inhibitors
- Classic Rett syndrome in a boy with R133C mutation of MECP2
- 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
- A Genome-Wide Association Study of Hypertension-Related Phenotypes in a Japanese Population
- Quadriceps sarcopenia and visceral obesity are risk factors for postural instability in the middle-aged to elderly population
- Associations between short one-leg standing time and speed of sound of calcaneal bone in a general population : The Shimanami Health Promoting Program (J-SHIPP) study
- An association of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and common carotid atherosclerosis
- 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
- Hypotension Associated with Prone Body Position : A Possible Overlooked Postural Hypotension
- Blood Pressure Is the Main Determinant of the Reflection Wave in Patients with Type 2 Diabetes
- An Association of 5, 10-Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism and Ischemic Stroke
- PE-284 Is Interleukin-10 Promoter Polymorphism Associated with Life-span? : The Ohasama Study(Preventive medicine/Epidemiology/Education-4 (H) PE48,Poster Session (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society
- Systemic Candidate Gebes Approach for Hypertension : on Behalf of the Study Group of Millennium Genome Project for Hypertension(Gene Therapy/Genetic Engineering (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Home Blood Pressure Is a Better Predictor of Carotid Atherosclerosis than Office Blood Pressure in Community-Dwelling Subjects