IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation (Q28114836)

3 January 2017

title

IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation (English)

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Potassium voltage-gated channel subfamily Q member 1

3 January 2017

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membrane repolarization during atrial cardiac muscle cell action potential

GOA release 2020-03-11

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GOA release 2020-03-11

author

Stig Haunsø

6

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Søren-Peter Olesen

8

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Jesper Hastrup Svendsen

7

Jesper Hastrup Svendsen

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Annette B Steffensen

Annette Buur Steffensen

1

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Lena Refsgaard

Lena Refsgaard

2

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Martin Nybo Andersen

Martin Nybo Andersen

3

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Morten Salling Olesen

Morten Salling Olesen

9

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Nicole Schmitt

Nicole Schmitt

10

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author name string

Cecilia Vallet

4

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3 January 2017

Amer Mujezinovic

5

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3 January 2017

publication date

1 July 2015

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Journal of Cardiovascular Electrophysiology

3 January 2017

published in

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3 January 2017

volume

26

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3 January 2017

issue

7

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3 January 2017

page(s)

715–723

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Heart Disease and Stroke Statistics--2010 Update: A Report From the American Heart Association

3 January 2017

cites work

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Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

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De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

21 January 2018

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

21 January 2018

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Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 January 2018

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High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

21 January 2018

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HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte

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Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.

21 January 2018

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Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization

21 January 2018

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Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

21 January 2018

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21 January 2018

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Cardiac potassium channel subtypes: new roles in repolarization and arrhythmia

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J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study

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Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization.

21 January 2018

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

21 January 2018

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

21 January 2018

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Autonomic control of cardiac action potentials: role of potassium channel kinetics in response to sympathetic stimulation.

21 January 2018

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Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

21 January 2018

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Potentiation of slow component of delayed rectifier K(+) current by cGMP via two distinct mechanisms: inhibition of phosphodiesterase 3 and activation of protein kinase G.

21 January 2018

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Changes in the mRNA levels of delayed rectifier potassium channels in human atrial fibrillation

21 January 2018

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In humans, chronic atrial fibrillation decreases the transient outward current and ultrarapid component of the delayed rectifier current differentially on each atria and increases the slow component of the delayed rectifier current in both

21 January 2018

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Chronic obstructive sleep apnea causes atrial remodeling in canines: mechanisms and implications

21 January 2018

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Familial Aggregation of Lone Atrial Fibrillation in Young Persons

21 January 2018

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Screening of KCNN3 in patients with early-onset lone atrial fibrillation

21 January 2018

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Prolonged Atrial Action Potential Durations and Polymorphic Atrial Tachyarrhythmias in Patients with Long QT Syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/JCE.12666

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