(Q28117761)

4 January 2017

title

Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) (English)

1 reference

Calcium voltage-gated channel auxiliary subunit alpha2delta 1

4 January 2017

main subject

1 reference

voltage-gated calcium channel activity involved in bundle of His cell action potential

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

7

0 references

Anita Rauch

8

0 references

Hugues Abriel

14

0 references

Jean-Sébastien Rougier

3

0 references

Charles Antzelevitch

object named as

Charles Antzelevitch

12

0 references

Thomas Lüscher

13

object named as

Thomas F. Lüscher

1 reference

4 January 2017

Christian Templin

1

1 reference

4 January 2017

Jelena-Rima Ghadri

2

1 reference

4 January 2017

Alessandra Baumer

4

1 reference

4 January 2017

Vladimir Kaplan

5

1 reference

4 January 2017

Maxime Albesa

6

1 reference

4 January 2017

Colleen Puleo

9

1 reference

4 January 2017

Dan Hu

10

1 reference

4 January 2017

Héctor Barajas-Martinez

11

1 reference

4 January 2017

Firat Duru

15

1 reference

4 January 2017

publication date

1 May 2011

1 reference

4 January 2017

published in

European Heart Journal

1 reference

4 January 2017

volume

32

1 reference

4 January 2017

issue

9

1 reference

4 January 2017

page(s)

1077–1088

1 reference

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

4 January 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Structure and regulation of voltage-gated Ca2+ channels

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

3D-Jury: a simple approach to improve protein structure predictions

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Membrane protein structure prediction. Hydrophobicity analysis and the positive-inside rule

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Short QT syndrome: from bench to bedside.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

A new look at calcium channel α2δ subunits

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Short QT syndrome: a review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Short QT syndrome: clinical findings and diagnostic-therapeutic implications

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Calcium channel gamma6 subunits are unique modulators of low voltage-activated (Cav3.1) calcium current

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Congenital short QT syndrome and implantable cardioverter defibrillator treatment: inherent risk for inappropriate shock delivery

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Sudden death associated with short-QT syndrome linked to mutations in HERG.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Short QT Syndrome: a familial cause of sudden death

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

A model recognition approach to the prediction of all-helical membrane protein structure and topology

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

29 September 2017

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR076

Low birth weight and increased sympathetic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR076

PI3K promotes voltage-dependent calcium channel trafficking to the plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR076

Calcium - a life and death signal

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR076

Idiopathic short QT interval: a new clinical syndrome?

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3086900

Short QT interval and short QT syndromes

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/21383000

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/21383000

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/EURHEARTJ/EHR076

1 reference

release_yik5csyo3fbgpbhfydxe7r6jxq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yik5csyo3fbgpbhfydxe7r6jxq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

1 reference

1 reference