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

Topic mentions per year

Topic mentions per year

1999-2018
012319992018

Papers overview

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2013
2013
Mutations or deletions of ACSL4 (FACL4, OMIM 300157) are a rare cause of non-syndromic X-linked intellectual disability. We… (More)
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2012
2012
BACKGROUND Brugada syndrome (BrS) is genetically heterogeneous. In Japanese BrS patients, except for SCN5A and KCNE5, mutations… (More)
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2012
2012
INTRODUCTION Potassium channel α-subunits encoded by KCNQ1-5 genes (Kv7) form voltage-dependent channels that can be modulated by… (More)
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2011
2011
BACKGROUND Brugada syndrome (BrS) has a significantly higher incidence among the male sex. Among genes coding ion channels and… (More)
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2008
2008
BACKGROUND Atrial fibrillation (AF) is the most common clinical arrhythmia and a major cause of cardiovascular morbidity and… (More)
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2006
2006
OBJECTIVES The function of Kv4.3 (KCND3) channels, which underlie the transient outward current I(to) in human heart, can be… (More)
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Highly Cited
2005
Highly Cited
2005
Voltage-gated potassium (K(V)) channels are modulated by at least three distinct classes of proteins including the KCNE family of… (More)
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2002
2002
The function of the KCNE5 (KCNE1-like) protein has not previously been described. Here we show that KCNE5 induces both a time… (More)
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2002
2002
X linked Alport syndrome (ATS, OMIM 301050) is a hereditary glomerulonephritis resulting from either point mutations or… (More)
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1999
1999
We describe the identification and characterization of a new gene deleted in the AMME contiguous gene syndrome. This gene is… (More)
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