Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation (Q28239461)

5

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Jesper Hastrup Svendsen

7

Jesper Hastrup Svendsen

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Morten Salling Olesen

Morten Salling Olesen

3

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Nicole Schmitt

Nicole Schmitt

8

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Bo Hjorth Bentzen

Bo Hjorth Bentzen

2

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author name string

Jonas Bille Nielsen

1

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Jens-Peter David

4

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language of work or name

English

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publication date

2014

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published in

Biomarkers in Medicine

1 reference

PubMed

volume

8

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issue

4

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page(s)

557-70

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cites work

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Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

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Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

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Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

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KCNE3 mutation V17M identified in a patient with lone atrial fibrillation

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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

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Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

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A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

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Atrial fibrillation: the role of common and rare genetic variants

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Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).

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The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome

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Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

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A method and server for predicting damaging missense mutations

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Dynamic partnership between KCNQ1 and KCNE1 and influence on cardiac IKs current amplitude by KCNE2

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KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

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KCNE2 is colocalized with KCNQ1 and KCNE1 in cardiac myocytes and may function as a negative modulator of I(Ks) current amplitude in the heart

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KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.

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K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

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A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

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Molecular determinants of cardiac transient outward potassium current (I(to)) expression and regulation

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Functional modulation of the transient outward current Ito by KCNE beta-subunits and regional distribution in human non-failing and failing hearts

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KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders

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Targeted deletion of kcne2 impairs ventricular repolarization via disruption of I(K,slow1) and I(to,f)

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KCNE2 and the K (+) channel: the tail wagging the dog

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Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesis

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Dynamic subunit stoichiometry confers a progressive continuum of pharmacological sensitivity by KCNQ potassium channels

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MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

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Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

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