(Q47671957)

4 February 2018

title

A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation (English)

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4 February 2018

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Jae Boum Youm

9

object named as

Jae Boum Youm

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4 February 2018

author name string

Chae Lim Jung

2

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4 February 2018

Hyun-ji Kim

3

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4 February 2018

Kwan-Hyuck Baek

4

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4 February 2018

Seung Jung Park

5

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4 February 2018

Young Keun On

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4 February 2018

Ki-Suk Kim

7

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4 February 2018

Su Jin Noh

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4 February 2018

June Soo Kim

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4 February 2018

Hana Cho

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4 February 2018

publication date

30 August 2013

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4 February 2018

published in

Pfluegers Archiv

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4 February 2018

volume

466

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4 February 2018

issue

3

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4 February 2018

page(s)

529-540

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4 February 2018

Atrial fibrillation: evidence for genetically determined disease

cites work

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A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

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R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

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Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

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Complex interactions between the sinoatrial node and atrium during reentrant arrhythmias in the canine heart

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Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel

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

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Tachybradycardia in the isolated canine right atrium induced by chronic sympathetic stimulation and pacemaker current inhibition.

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Pro-arrhythmogenic effects of the S140G KCNQ1 mutation in human atrial fibrillation - insights from modelling.

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Cholesterol inhibits M-type K+ channels via protein kinase C-dependent phosphorylation in sympathetic neurons

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

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Common variants at ten loci influence QT interval duration in the QTGEN Study

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Mathematical model of an adult human atrial cell: the role of K+ currents in repolarization

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

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

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The role of S4 charges in voltage-dependent and voltage-independent KCNQ1 potassium channel complexes

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Altered HCN4 channel C-linker interaction is associated with familial tachycardia-bradycardia syndrome and atrial fibrillation

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12 December 2020

Single cells isolated from human sinoatrial node: action potentials and numerical reconstruction of pacemaker current.

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12 December 2020

Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1.

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12 December 2020

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation

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12 December 2020

Molecular genetics of atrial fibrillation

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12 December 2020

10.1007/S00424-013-1337-6

Identifiers

DOI

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4 February 2018

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4 February 2018