KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome? (Q34547008)

2 August 2017

KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome? (English)

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2 August 2017

Annukka M Lahtinen

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2 August 2017

Annukka Marjamaa

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2

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2 August 2017

Heikki Swan

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2 August 2017

Kimmo Kontula

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2 August 2017

18 January 2011

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2 August 2017

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2 August 2017

12

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2 August 2017

11

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https://scigraph.springernature.com/pub.10.1186/1471-2350-12-11

2 August 2017

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cites work

The genetic basis of long QT and short QT syndromes: a mutation update

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

7 July 2018

1 reference

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High prevalence of four long QT syndrome founder mutations in the Finnish population

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3032654

Common candidate gene variants are associated with QT interval duration in the general population

7 July 2018

1 reference

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The QT syndromes: long and short

7 July 2018

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Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

7 July 2018

1 reference

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Risk stratification in the long-QT syndrome.

7 July 2018

1 reference

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3032654

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

7 July 2018

1 reference

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IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

7 July 2018

1 reference

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The role of the IsK protein in the specific pharmacological properties of the IKs channel complex

7 July 2018

1 reference

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A minK-HERG complex regulates the cardiac potassium current I(Kr)

7 July 2018

1 reference

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3032654

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3032654

Sex differences in the evolution of the electrocardiographic QT interval with age

7 July 2018

1 reference

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Compound mutations: a common cause of severe long-QT syndrome.

7 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Mice display sex differences in halothane-induced polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Acute effects of oestrogen on the guinea pig and human IKr channels and drug-induced prolongation of cardiac repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-11

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

21 January 2018

1 reference

12 December 2020

Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families

1 reference

12 December 2020

Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients

1 reference

12 December 2020

Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes

1 reference

12 December 2020

A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics

1 reference

12 December 2020

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-12-11

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Dimensions Publication ID

2 August 2017

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2 August 2017

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