Takano Makoto | 自治医科大学生理学

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
Ion channel mutations and polymorphisms in Japanese patients with acquired long QT syndrome
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)

スポンサーリンク