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KCNE5 gene

Known as: POTASSIUM CHANNEL, VOLTAGE-GATED, ISK-RELATED FAMILY, MEMBER 1-LIKE, KCNE5, potassium voltage-gated channel subfamily E regulatory subunit 5 
National Institutes of Health

Papers overview

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2020
2020
Gene expression profile in cases of infectious death in infancy
Background Genetic predispositions in cases suffering sudden unexpected infant death have been a research focus worldwide during… 
2015
2015
Comparison of the Transcriptomes of Mouse Skin Derived Precursors (SKPs) and SKP-Derived Fibroblasts (SFBs) by RNA-Seq
Skin-derived precursors (SKPs) from dermis possess the capacities of self-renewal and multipotency. In vitro and in vivo studies… 
2012
2012
KCNE5 Polymorphism rs697829 is Associated with QT Interval and Survival in Acute Coronary Syndromes Patients
KCNE5 Gene Variant, QTc and Survival in ACS. Introduction: The KCNE family is a group of small transmembrane channel proteins… 
2012
2012
OS081. Novel KCNQ3/KCNE5 isoform protein and mRNA expression in first trimester human placentae.
2011
2011
KCNE5 Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation
Brugada syndrome (BrS) and idiopathic ventricular fibrillation (IVF) have a higher incidence among males. Among genes coding ion… 
2008
2008
Atrial Fibrillation Genetic Considerations: The Basic Scientist's Perspective
Common atrial fibrillation (AF) is a complex disease, and its pathogenesis involves multiple genetic factors, environmental… 
2007
2007
The phenotype of a KCNQ1 mutation depends on its KCNE partners: is the cardiac slow delayed rectifier (IKs) channel more than a KCNQ1/KCNE1 complex?
2006
2006
Abstract 3394: Gain of Function in IKs Secondary to a Mutation in KCNE5 as a Cause of Atrial Fibrillation
2005
2005
69 T97C and C193T substitutions in KCNE5: two genetic risk factors for atrial fibrillation
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