QT syndrome - Globe Thesis

Keyword [QT syndrome] Result: 1 - 20 \| Page: 1 of 4
1.	Molecualr Genetics Of Klippel-Trenaunay Syndrome And Long QT Syndrome
2.	KCNJ5 Gly387Arg Mutation Responsible For Familial Long QT Syndrome
3.	Study Of Molecular Determinants And Function Of HERG Channels Interacting With Agents In Acquired Long QT Syndrome
4.	Risk Factor Research Of Malignant Arrhythmia
5.	Studies On Cause Of LQTS By KCNQ1 Mutant And Ethanol Effect On KCNQ1 Channel
6.	Cellular And Ionic Mechanisms Of Dauricine And Daurisoline On Acquired Long QT Syndrome
7.	The Role Of Gap Junction Alteration In Ventricular Arrhythmogenasis Induced By Drugs
8.	Role Of Gap Junction In Ventricular Arrhythmias Of Long QT Syndrome
9.	KCNE2 Modulates The Function Of Transient Outword Potassium Current And Electrophysiological Properties In Cadiomyocytes
10.	Propofol Inhibits Currents Of Both Human Ether-a-go-go-related Gene And Its Non-sense Mutation, Q738X, In HEK293 Cells
11.	The Regulation And The Mechanism Of Estrogen On L Type Calcium And Sodium Calcium Exchanger In Cardiomyocytes
12.	Study Of Mechanism Of Ventricular Arrhythmias In The Short QT Duration Syndrome
13.	Molecular Genetic And Cellular Electrophysiological Study Of Short QT Syndrome
14.	A Novel Mechanism For Long QT Syndrome Mutations In KCNQ1 Gene And The Effects Of Ethanol On KCNQ1 Channel
15.	Preliminary Simulation Study Of The Electrophysiological Mechanisms Of Short QT Syndrome
16.	Effects Of AAP10 On Ventricular Arrhythmia In Rabbit LQT2 Model
17.	1. Association Between Atrial Fibrillation And Chronic Helicobacter Pylori Infection Or C-reactive Protein 2. Low-Dosage Epinephrine Effects On The Cardiac Repolarization In Chinese Normal Young Subjects And Patients With Syncope
18.	KCNQ1 V254M Mutation In Romano-Ward Syndrome
19.	The Mutation Screening And Primary Functional Study On The Cadidate Gene Of Familial Progressive Cardiac Conduction Defect With Long QT Syndrome
20.	Study On The Effects And Mechanisms Of Dauricine And Daurisoline For Acquired Long QT Syndrome
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