Screening of the ito regulatory subunit klf15 in patients with early-onset lone atrial fibrillation (Q36850495)

16 August 2017

Screening of the ito regulatory subunit klf15 in patients with early-onset lone atrial fibrillation (English)

1 reference

16 August 2017

1 reference

Jesper Hastrup Svendsen

5

object named as

Jesper Hastrup Svendsen

0 references

Stig Haunsø

4

object named as

Stig Haunsø

1 reference

16 August 2017

Lena Refsgaard

3

0 references

Morten Salling Olesen

object named as

Morten Salling Olesen

2

0 references

author name string

Morten Wagner Nielsen

1

1 reference

16 August 2017

17 May 2013

1 reference

16 August 2017

Frontiers in Genetics

1 reference

16 August 2017

4

1 reference

16 August 2017

88

1 reference

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

Circadian rhythms govern cardiac repolarization and arrhythmogenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

KCNQ1 gain-of-function mutation in familial atrial fibrillation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

New ideas about atrial fibrillation 50 years on.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of I(to) and confers susceptibility to ventricular tachycardia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3656344

Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23730307

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3389/FGENE.2013.00088

1 reference

16 August 2017

1 reference

PMC publication ID

3656344

16 August 2017

PubMed publication ID

23730307

1 reference

PMC publication ID

3656344