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Publications by Kenshi HAYASHI

Clinical and Electrophysiological Characterization of a Novel Mutation (F193L) in the KCNQ1 Gene Associated With Long QT Syndrome

Clinical Science
Medicine
2003English

Development of Transducer Materials of a Taste Sensor With Langmuir-Blodgett Method

Transactions of the Society of Instrument and Control Engineers
1993English

Related publications

R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation

Heart Rhythm
Cardiovascular MedicinePhysiologyCardiology
2011English

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature Among Iranian Long QT Families

Iranian Biomedical Journal
BiochemistryClinical BiochemistryGeneticsMolecular Biology
2019English

Clinical, Genetic, and Biophysical Characterization of a Homozygous HERG Mutation Causing Severe Neonatal Long QT Syndrome

Pediatric Research
Child HealthPediatricsPerinatology
2003English

Overlapping LQT1 and LQT2 Phenotype in a Patient With Long QT Syndrome Associated With Loss-Of-Function Variations in KCNQ1 and KCNH2

Biophysical Journal
Biophysics
2010English

Impaired KCNQ1-KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome

Circulation Research
Cardiovascular MedicinePhysiologyCardiology
2005English

Novel Arrhythmogenic Mechanism Revealed by a Long-Qt Syndrome Mutation in the Cardiac Na+ Channel

Circulation Research
Cardiovascular MedicinePhysiologyCardiology
2001English

A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome

Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
Nuclear MedicineRadiologyOral SurgeryImagingDentistryForensic MedicinePathologySurgery
2018English

Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome

International Journal of Cardiology
Cardiovascular MedicineCardiology
2013English

Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-Qt Syndrome Genotype-Phenotype Correlations of the KCNQ1(S349W) Mutation

Journal of Cardiovascular Electrophysiology
Cardiovascular MedicinePhysiologyCardiology
2010English

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