スポンサーリンク
Division Of Cardiology Department Of Internal Medicine National Cardiovascular Center | 論文
- PJ-179 Mechanisms Underlying the Impairment of Ischemia-induced Neovascularization in Aging Mice : the Pivotal Role for Matirx-Metalloproteinase-2(Regeneration(angiogenesis/myocardial regeneration)(04)(M),Poster Session(Japanese),The 72nd Annual Scientifi
- PJ-039 Treatment of ApoE-Deficient Mice with Statin Inhibits the Oxidative Stress-dependent Lysosomal Protease Cathepsin Activation System : Implication for Plaque Stability(Atherosclerosis, basic(05)(IHD),Poster Session(Japanese),The 72nd Annual Scientif
- PJ-485 Superiority of Cardiac MIBG Clearance Rate to Conventional Parameters in Predicting Effectiveness of Beta-Blocker Therapy for Patients with Dilated Cardiomyopathy(Heart failure, clinical-12, The 71st Annual Scientific Meeting of the Japanese Circul
- 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-118 Seasonal Pattern of Occurrence of Cardiac Events in Genotyped Patients with Congenital Long QT Syndrome(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Cir
- 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
- PJ-591 Histologic Reconstruction of the Postero-inferior Atrioventricular Septal Junction : With Reference to Autopsy Finding of Atrioventricular Reentrant Tachycardia(Arrhythmia, diagnosis/Pathophysiology/EPS(15)(A),Poster Session(Japanese),The 72nd Annu
- PJ-577 The targeting of cyclophilin D by RNA interference as a novel therapeutic strategy against myocardial ischemia/reperfusion injury(Acute coronary syndrome, basic/clinical(05)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Ja
- 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
- PJ-042 Pivotal Roles of CYLD (cylindromatosis) as a Deubiquitinating Enzyme in Vasculature(Atherosclerosis, basic(05)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
スポンサーリンク