(Q33162279)

23 July 2017

title

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation (English)

1 reference

familial atrial fibrillation

23 July 2017

main subject

1 reference

1 reference

Rachel Bastiaenen

3

0 references

Brian P. Delisle

Brian P Delisle

12

0 references

Michael H. Gollob

Michael H Gollob

5

0 references

Elijah Behr

Elijah R Behr

9

0 references

Pascale Guicheney

Pascale Guicheney

11

0 references

Michael J Ackerman

10

Michael J Ackerman

1 reference

23 July 2017

1

Daniel C Bartos

1 reference

23 July 2017

Jeffrey B Anderson

2

1 reference

23 July 2017

Jonathan N Johnson

4

1 reference

23 July 2017

David J Tester

6

1 reference

23 July 2017

Don E Burgess

7

1 reference

23 July 2017

Tessa Homfray

8

1 reference

23 July 2017

publication date

25 January 2013

1 reference

Journal of Cardiovascular Electrophysiology

23 July 2017

published in

1 reference

23 July 2017

volume

24

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23 July 2017

issue

5

1 reference

23 July 2017

page(s)

562-569

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

23 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome

21 June 2018

1 reference

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Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1.

21 June 2018

1 reference

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Simulation of the undiseased human cardiac ventricular action potential: model formulation and experimental validation

21 June 2018

1 reference

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

21 June 2018

1 reference

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Therapeutic strategies for long-QT syndrome: does the molecular substrate matter?

21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

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

21 June 2018

1 reference

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Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

KCNE peptides differently affect voltage sensor equilibrium and equilibration rates in KCNQ1 K+ channels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

Status of the epidemiology of atrial fibrillation

21 June 2018

1 reference

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Molecular basis of arrhythmias

21 June 2018

1 reference

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Subunit interaction determines IKs participation in cardiac repolarization and repolarization reserve

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

Phosphorylation of the A-kinase-anchoring protein Yotiao contributes to protein kinase A regulation of a heart potassium channel

21 June 2018

1 reference

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A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

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

21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

KCNE4 is an inhibitory subunit to the KCNQ1 channel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

A constitutively open potassium channel formed by KCNQ1 and KCNE3

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3640728

A population-based study of the long-term risks associated with atrial fibrillation: 20-year follow-up of the Renfrew/Paisley study.

21 June 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome

21 January 2018

1 reference

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

21 January 2018

1 reference

Temporal Relations of Atrial Fibrillation and Congestive Heart Failure and Their Joint Influence on Mortality

21 January 2018

1 reference

SCN5A mutations in atrial fibrillation

21 January 2018

1 reference

12 December 2020

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

1 reference

12 December 2020

Regulation of a heart potassium channel by protein kinase A and C

1 reference

12 December 2020

The natural history of atrial fibrillation: incidence, risk factors, and prognosis in the Manitoba Follow-Up Study

1 reference

12 December 2020

Mechanisms of atrial fibrillation: mother rotors or multiple daughter wavelets, or both?

1 reference

12 December 2020

AN EXPERIMENTAL STUDY OF CONCEALED CONDUCTION

1 reference

12 December 2020

Identifiers

DOI

10.1111/JCE.12068

1 reference

23 July 2017

1 reference

23 July 2017

1 reference