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自治医科大学 生理学 | 論文
- NRSF regulates the developmental and hypertrophic changes of HCN4 transcription in rat cardiac myocytes
- 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))
- 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
- AFTERNOON TEA
- Ion channel mutations and polymorphisms in Japanese patients with acquired long QT syndrome
- 心臓イオンチャネル遺伝子の転写制御機構 : エピジェネティックスと機能分化
- IS086 Novel missense mutation in the Pore region of HERG gene in Long QT syndrome Patient
- Role of KCNQ1 in the Cell Swelling-Induced Enhancement of the Slowly Activating Delayed Rectifier K^+ Current
- High-risk for Bradyarrhythmic Complications in Patients with Brugada Syndrome Caused by SCN5A Gene Mutations(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)