KANEDA Makoto | Department of Information Physiology, National Institute for Physiological Sciences
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Department of Information Physiology, National Institute for Physiological Sciences | 論文
- Point-Mutations Related to the Loss of Batrachotoxin Binding Abolish the Grayanotoxin Effect in Na^+ Channel Isoforms
- Arrhythmogenesis in the Short-QT Syndrome Associated With Combined HERG Channel Gating Defects : A Simulation Study
- Current Perspective : Dissecting Receptor-Mediated Ca^ Influx Pathways : TRP Channels and Their Native Counterparts
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-600 Lidocaine Prevents Brugada Syndrome with the N406S Mutation of SCN5A from Going into the Intermediate Inactivation(Arrhythmia, basic-5 (A) PJ101,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation So