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KCNH2 gene

Known as: POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2, Kv11.1, ETHER-A-GO-GO-RELATED GENE, HUMAN 
National Institutes of Health

Related topics

Related topics

2 relations
ERG1 Potassium ChannelKCNV2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
Mechanisms and Clinical Relevance of Drug-Induced Long QT Syndrome: Block of hERG, Drug Metabolism and Drug Transport in the Human Heart
Long QT Syndrome (LQTS) is a serious cardiac disorder that can derive from both congenital and drug-induced circumstances… 
2018
2018
Development of ( 6 R ) ‐ 2-Nitro-6-[ 4-( tri fl uoromethoxy )
Discovery of the potent antileishmanial effects of antitubercular 6-nitro-2,3-dihydroimidazo[2,1-b][1,3]oxazoles and 7… 
Review
2016
Review
2016
The faint source population at 15.7 GHz – III. A high-frequency study of HERGs and LERGs
A complete sample of 96 faint ($S > 0.5$ mJy) radio galaxies is selected from the Tenth Cambridge (10C) survey at 15.7~GHz… 
Review
2016
Review
2016
Cardiovascular safety of tyrosine kinase inhibitors: Putting their “QT-phobia” in perspective
Many potentially valuable drugs, including protein kinase inhibitors (PKI), risk being dropped from further development, without… 
2012
2012
hERG 1 Channels and Glut1 as Independent Prognostic Indicators of Worse Outcome in Stage I and II Colorectal Cancer : A Pilot Study 1
BACKGROUND: There is a need to identify new markers to assess recurrence risk in early-stage colorectal cancer (CRC) patients. We… 
2011
2011
Electrophysiological study of V535M hERG mutation of LQT2
SummaryThis study examined the current changes of human ether-a-go-go-related gene (hERG) mutation derived from a LQT2 Chinese… 
2008
2008
Inhibition of cardiac hERG potassium channels by tetracyclic antidepressant mianserin
The antidepressant mianserin exhibits a tetracyclic structure that is different from typical tricyclic antidepressants (TCA) and… 
2001
2001
Molecular biology and cellular mechanisms of cardiac arrhythmias and sudden death in infants and young children
Abstract Sudden cardiac death accounts for 19% of sudden deaths in children between 1 and 13 years of age and 30% of sudden… 
2000
2000
Novel mechanism of HERG current suppression in LQT2 : Shift in voltage dependence of HERG inactivation
2000
2000
The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family.
BACKGROUND Long QT syndrome is a congenital abnormality of cardiac repolarization causing syncope and sudden death from…