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Publications by Guo Qi Teng
Homozygous Missense N629D hERG (KCNH2) Potassium Channel Mutation Causes Developmental Defects in the Right Ventricle and Its Outflow Tract and Embryonic Lethality
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
Novel Gain-Of-Function Mechanism in K+ Channel-Related Long-Qt Syndrome: : Altered Gating and Selectivity in the HERG1 N629D Mutant
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
Related publications
Potassium Channel Kv11.1 (KCNH2)
Science-Business eXchange
Molecular and Functional Characterization of Common Polymorphisms in HERG (KCNH2) Potassium Channels
American Journal of Physiology - Heart and Circulatory Physiology
Cardiovascular Medicine
Physiology
Cardiology
Long-Qt Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Mechanisms of hERG Potassium Channel Enhancers
Biophysical Journal
Biophysics
Biomimetic Membrane Platform Containing hERG Potassium Channel and Its Application to Drug Screening
Analyst, The
Biochemistry
Environmental Chemistry
Analytical Chemistry
Electrochemistry
Spectroscopy
Right Ventricular Outflow Tract Tachycardias
Arrhythmia
Right Ventricular Outflow Tract Obstruction
Canadian Journal of Anaesthesia
Medicine
Anesthesiology
Pain Medicine
Urinary Bladder Matrix Promotes Site Appropriate Tissue Formation Following Right Ventricle Outflow Tract Repair
Organogenesis
Developmental Biology
Embryology
Biomedical Engineering
Transplantation
Benign Neoplasms in the Right Ventricular Outflow Tract
Baylor University Medical Center Proceedings
Medicine
