(Q35830168)

English

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

scientific article published on 23 December 2011

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scholarly article

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Europe PubMed Central

PMC publication ID

10 August 2017

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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long QT syndrome

1 reference

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inferred from title

object named as

Wino J Wijnen

12

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Michael W Tanck

object named as

Michael W Tanck

7

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16

object named as

Arthur A M Wilde

1 reference

Europe PubMed Central

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10 August 2017

Michael J Ackerman

17

object named as

Michael J Ackerman

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

Ahmad S Amin

1

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Europe PubMed Central

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10 August 2017

John R Giudicessi

2

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Europe PubMed Central

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10 August 2017

Anke J Tijsen

3

1 reference

Europe PubMed Central

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10 August 2017

Anne M Spanjaart

4

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Europe PubMed Central

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10 August 2017

Yolan J Reckman

5

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Europe PubMed Central

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10 August 2017

Christine A Klemens

6

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Europe PubMed Central

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10 August 2017

Jamie D Kapplinger

8

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Europe PubMed Central

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10 August 2017

Nynke Hofman

9

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Europe PubMed Central

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10 August 2017

Moritz F Sinner

10

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Europe PubMed Central

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10 August 2017

Martina Müller

11

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10 August 2017

Hanno L Tan

13

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Europe PubMed Central

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10 August 2017

Connie R Bezzina

14

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Europe PubMed Central

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10 August 2017

Esther E Creemers

15

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Europe PubMed Central

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10 August 2017

Yigal M Pinto

18

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10 August 2017

publication date

23 December 2011

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Europe PubMed Central

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10 August 2017

European Heart Journal

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Europe PubMed Central

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10 August 2017

33

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10 August 2017

6

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10 August 2017

714-723

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Europe PubMed Central

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10 August 2017

Gene silencing by microRNAs: contributions of translational repression and mRNA decay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Regulation of cardiac gene expression by KLF15, a repressor of myocardin activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

NOS1AP is a genetic modifier of the long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Clinical practice. Long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Allele-specific targeting of microRNAs to HLA-G and risk of asthma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Natural selection on human microRNA binding sites inferred from SNP data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Conditional differentiation of heart- and smooth muscle-derived cells transformed by a temperature-sensitive mutant of SV40 T antigen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

11 July 2018

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3303714

24 September 2018

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR473

21 January 2018

Identifiers

10.1093/EURHEARTJ/EHR473

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

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