| Receipt no. | First name | Last name | Abstract title |
|---|
| 10043 | Yoshihiro | Tanaka | Functional Analysis of hERG1 Mutations Using ECG in Larval Zebrafish Model of Long QT Syndrome Type 2 |
| 10086 | Peili | Li | Epigenetic and post-translational modification of hERG to control the channel protein expression and function |
| 10106 | Ryo | Endo | Stabilization of Kv1.5 Channel Protein by Olprinone as a chemical chaperone |
| 10148 | Yusuke | Fujii | RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes |
| 10463 | Shunsuke | Tomomori | Common variant in PITX2 contributes to the pathogenesis of atrial fibrillation by impairing sinus node function |
| 10717 | Jun | Oikawa | Anti-oxidant compound suppresses the construction of arrhythmogenic substrate in the isoproterenol induced acute myocardial injury |
| 10951 | Takehito | Kondo | Heat Shock Factor-1 but not Another Family Member Stabilizes the Novel Mutant A78T-HERG Protein from a LQT2 Patient |
| 11620 | Michinori | Hirano | Development of a Novel Shock Wave Catheter Ablation System -A Preclinical Validation Study- |
| 12662 | Taisuke | Ishikawa | Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPs Identified in a Brugada Syndrome Family with Different Expressivity |
| 12906 | Yasutaka | Kurata | Electrophysiological Properties of iPS Cell-Derived Cardiomyocytes from a Patient with LQT1 Harboring the Novel Mutation M437V of KCNQ1 |
| 13404 | Hiroya | Matsumura | SCN5A H558R Polymorphism Counteracts Effects of SCN5A Mutations by Decrease Risk Allele Expression Level |
| 13580 | Yosuke | Hayashi | The occurrence of ectopy from pulmonary veins in atrial fibrillation in middle-aged women |
| 13778 | Masaya | Watanabe | LED flash-induced termination of anatomical reentry in optogenetically modified transverse rat ventricular tissue slices |
| 13842 | Takeshi | Harita | The Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Long QT Syndrome type 8 Patients without Extracardiac Phenotypes |
| 13887 | Suguru | Nishiuchi | Abnormal Expressions of Cardiac Ion Channels-associated Genes in Lamin A/C-related Cardiomyopathy-specific Induced Pluripotent Stem Cell-derived Cardiomyocytes |
| 20061 | Irma | Maghfirah | Correlation between SCN5A Gene Mutation and Occurence of Ventricular Fibrillation in Brugada Syndrome |
