Kawamura Mihoko | Department Of Cardiovascular And Respiratory Medicine Shiga University Of Medical Science

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著作論文

Genetic Variations and Haplotypes of ABCC2 Encoding MRP2 in a Japanese Population
Genetic Variations of the ABC Transporter Gene ABCB11 Encoding the Human Bile Salt Export Pump (BSEP) in a Japanese Population
日本人におけるGSTT1及びGSTM1の遺伝子多型の同定及びハプロタイプ構造の解析
Twenty Novel Genetic Variations and Haplotype Structures of the DCK Gene Encoding Human Deoxycytidine Kinase (dCK)
Genetic Variations of VDR/NR1I1 Encoding Vitamin D Receptor in a Japanese Population
Inhibition of Cardiac Remodeling by Pravastatin Is Associated with Amelioration of Endoplasmic Reticulum Stress
Plasma Adiponectin Is Associated with Plasma Brain Natriuretic Peptide and Cardiac Function in Healthy Subjects
Atorvastatin Slows the Progression of Cardiac Remodeling in Mice with Pressure Overload and Inhibits Epidermal Growth Factor Receptor Activation
Genetic Variations of CYP2C9 in 724 Japanese Individuals and Their Impact on the Antihypertensive Effects of Losartan
PE-166 Superoxide-Dependent Activation of Cathepsin System is Associated with Hypertensive Myocardial Remodeling and Represents a Target for AT1R Blocker Therapy(Cardiovascular pharmacology, basic/clinical(03)(H),Poster Session(English),The 72nd Annual Sc
PJ-677 Comparison of Bypass Surgery with Drug-Eluting Stents for Diabetic Patients with Left Main Coronary Artery (LMCA) Stenosis(PJ114,Coronary Revascularization, PCI (DES) 4 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japan
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
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
Genetic Polymorphisms of Copper- and Platinum Drug-efflux Transporters ATP7A and ATP7B in Japanese Cancer Patients
Ethnic Differences of two Non-synonymous Single Nucleotide Polymorphisms in CDA Gene
Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome
Genetic Polymorphisms of FCGRT Encoding FcRn in a Japanese Population and Their Functional Analysis
Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome
Carvedilol, a Non-Selective β-with α_1-Blocker is Effective in Long QT Syndrome Type 2
Serum Blood Urea Nitrogen and Plasma Brain Natriuretic Peptide and Low Diastolic Blood Pressure Predict Cardiovascular Morbidity and Mortality Following Discharge in Acute Decompensated Heart Failure Patients
Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia
Mutation Analysis of the KCNJ8 Gene in Japanese Patients with J-Wave Syndrome and Idiopathic Ventricular Fibrillation
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

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