Yamada Yoshiji | Department Of Gene Therapy Gifu International Institute Of Biotechnology And Institute Of Applied Bi

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著作論文

OE-292 Genetic Risk for Coronary Artery Disease in Low-Risk or High-Risk Subjects Defined by Conventional Risk Factors(Genetics/Genetically Engineered Models 2 (H) : OE36)(Oral Presentation (English))
Genetic Risk Diagnosis for Coronary Artery Spasm
PPAR Alpha Agonist Prevents the Development of cardiac Hypetrophy and the Progression of Heart Failure by Suppressing Inflammatory Responses(Heart Failure, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Activation of a Calcineurin-Dependent Pathway for Cardiac Hypertrophy in Cardiac-Specific Calmodulin Overexpressing Mice
ZAK1-4β Inhibits Calcineurin Activity and Is Expressed Independently of ZAKI-4α and DSCR1 in Rat Cardiomyocytes
AT_1 Receptor Blockade Attenuates Activation of Calcineurin and Development of Cardiac Hypertrophy and Fibrosis in Dahl-Salt Hypertension
Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension
PJ-437 Genetic Factors for Ischemic and Hemorrhagic Stroke in Japanese Individuals(PJ074,Cerebrovascular Circulation/Stroke (H),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
DPE-004 Associations of Genetic Variants with Ischemic Stroke in Japanese Individuals with Metabolic Syndrome(DPE01,Metabolic Syndrome (H),Digital Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
PE-544 Associations of Genetic Variants with Myocardial Infarction in Japanese Individuals with Chronic Kidney Disease(PE091,Molecular Biology (M),Poster Session (English),The 73rd Annual Scientific Meeting of the Japanese Circulation Society)
OJ-164 Association of a Polymorphism of the Apolipoprotein E Gene with Chronic Kidney Disease in Japanese Individuals with Metabolic Syndrome(OJ28,Kidney/Renal Circulation/CKD 1 (H),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Ja
OJ-163 Association of Genetic Variants with Chronic Kidney Disease in Japanese Individuals(OJ28,Kidney/Renal Circulation/CKD 1 (H),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
OE-203 Identification of Polymorphisms of the Apolipoprotein A-V Gene as Genetic Risk Factors for Metabolic Syndrome(OE35,Metabolic Syndrome (H),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
PE-352 Genetic Risk for low HDL-cholesterol or high LDL-cholesterol Concentrations(Lipid disorders(03)(H),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OJ-254 Assessment of Genetic Factors for Obesity(Diabetes / Obesity / Metabolic syndrome(03)(H),Oral Presentation (Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OE-331 Association of Polymorphisms of ABCA1 and ROS1 with Hypertension in Japanese Individuals(Hypertension, clinical(02)(H),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OE-211 Assessment of Genetic Risk for Hypertriglyceridemia(Lipid disorders(01)(H),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OE-073 Assessment of Genetic Risk for Thoracic Aortic Aneurysm among Hypertensive Patients(Heart failure, clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OE-072 Genetic Risk for Myocardial Infarction in Japanese Indivisuals(Heart failure, clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
FRS-090 Genetic Risk for Metabolic Sndrome : Examination of Canditate Gene Polymorphisms related to Lipid Metabolism in Japanese Individuals(New Insights into Metabolic Syndrome(01)(H),Featured Research Session,The 72nd Annual Scientific Meeting of the Ja
OE-210 Mitochondrial Haplogroup N9b is Protective against Myocardial Infarction in Japanese Males(Genetics/Genetically engineered models/Gene therapy-1(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OE-207 Association of Gene Polymorphisms with Myocardial Infarction among Men or Women or among Individuals with or without Coronary Risk Factors(Genetics/Genetically engineered models/Gene therapy-1(H/M), The 71st Annual Scientific Meeting of the Japanes
PJ-622 Genetic Risk for Myocardial Infarction in Individuals with Low Serum HDL-Cholesterol Levels(Genetics/Genetically engineered models/Gene therapy-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-557 Prediction of Genetic Risk for Metabolic Syndrome(Preventive medicine/Epidemiology/Education-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-512 Assessment of the Genetic Component of Hypertension(Hypertension, clinical-07, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-501 Assessment of Genetic Risk for Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-3, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-500 Genetic Risk for Lone Atrial Fibrillation(Genetics/Genetically engineered models/Gene therapy-3, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-393 Genetic Risk for Ischemic and Hemorrhagic Stroke(Cerebrovascular circulation/Stroke-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Distribution of Geriatric Disease-Related Genotypes in the National Institute for Longevity Sciences, Longitudinal Study of Aging (NILS-LSA)
Association of a G^ → T (Val^ → Phe) polymorphism of the plasma platelet-activating factor acetylhydrolase gene with myocardial damage in Japanese patients with nonfamilial hypertrophic cardiomyopathy
Association of polymorphisms of SORBS1, GCK and WISP1 with hypertension in community-dwelling Japanese individuals
Association of a polymorphism of the dopamine receptor D4 gene with bone mineral density in Japanese men
Association of polymorphisms of paraoxonase 1 and 2 genes,alone or in combination, with bone mineral density in community-dwelling Japanese
Association of a polymorphism of the transforming growth factor-β1 gene with blood pressure in Japanese individuals
Identification of genetic factors and development of genetic risk diagnosis systems for cardiovascular diseases and stroke
Association Between a Polymorphism of the Transforming Growth Factor-β1 Gene and Genetic Susceptibility to Ossification of the Posterior Longitudinal Ligament in Japanese Patients
Identification of Genetic Factors and Development of Genetic Risk Diagnosis Systems for Cardiovascular Diseases(Japan Heart Foundation Satoh Memorial Award Lecture,The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
Hyper-Phosphorylated Retinoblastoma Protein Suppresses Telomere Elongation
Roles of Plasma Platelet-Activating Factor Acetylhydrolase in Allergic, Inflammatory, and Atherosclerotic Diseases
1 Identification of Genetic Risk and Development of Personalized Prevention Systems for Cardiovascular Diseases(Plenary Session 7 (PL-7) (M) Genomic Approaches to Cardiovascular Diseases : Present and Future,Special Program,The 72nd Annual Scientific Meet

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