long QT syndrome - Globe Thesis

Keyword [long QT syndrome] Result: 41 - 60 \| Page: 3 of 4
41.	The Role Of UGGT1 And GLUⅡβ Playing In The Long QT Syndrome-Associated A561V Mutations
42.	The Clinical And Molecular Genetics Of A Chinese Family With Long QT Syndrome
43.	Electrophysiological Characterization Of A Small Molecular Activator On Human Ether-a-go-go-related Gene(hERG) Potassium Channel
44.	Pathogenesis Of LQT2 Syndrome Caused By HERG F68C Mutation
45.	Clinical Study Of Acquired Long QT Syndrome In Patients With Chronic Kidney Disease
46.	The Effect Of MiR-103a-3p On Ikr Encoded By HERC Gene
47.	A New Discovery Of Pathogenic Genes In China For Congenital Long QT Interphase Syndrome Subtype JLN Syndrome
48.	Frequency, temporal onset of occurrence and risk factor identification for acquired long QT syndrome in a critical care population
49.	Structure, function, and pharmacology of the cardiac sodium channel: Implications for the Long QT syndrome
50.	Structure and function relationship of the potassium I(Ks) channel and its relation to long QT syndrome
51.	Functional analysis of hERG potassium channels and mutations underlying the Long QT Syndrome
52.	Long QT syndrome G760A single nucleotide polymorphism detection using planar waveguide technology
53.	Development of Genetic Goat and Hamster Models of Atrial Fibrillation and Long QT Syndrome; and Genetic Hamster Models of Middle East Respiratory Syndrome
54.	Improving Patient-Specific Diagnostics for KCNQ1-mediated Long QT Syndrome
55.	The Arrthymic Pathogenesis Of Gene Variants In KCNQ1 And SCN10A
56.	Studying Mechanism Of Pathogenicity Regulation Related To Development And Differentiation In Type 7 Long QT Syndrome Using Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes
57.	Mutation Spectrum And Clincal Features Of Congenital Long QT Syndrome In Children:a Single Center Follow-up Study
58.	Clinical Analysis Of Five Families With Hereditary Long QT Syndrome
59.	The Role Of Endoplasmic Reticulum Stress Playing In The Misfolding And Trafficking Defect Of HERG-A561V Mutations
60.	The Associations Between Location Of Mutation In The KCNQ1 And Phenotypic Presentation Of Congenital Long QT Syndrome Type 1: Meta-Analysis
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