Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias (Q24311437)

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14 October 2019

title

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias (English)

1 reference

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voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization

14 October 2019

main subject

heart arrhythmia

0 references

2 references

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:1902282

Potassium voltage-gated channel subfamily Q member 1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

0 references

11

1 reference

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14 October 2019

author name string

Wang Q

1

1 reference

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14 October 2019

Curran ME

2

1 reference

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14 October 2019

Splawski I

3

1 reference

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14 October 2019

Burn TC

4

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14 October 2019

Millholland JM

5

1 reference

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14 October 2019

VanRaay TJ

6

1 reference

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14 October 2019

Shen J

7

1 reference

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14 October 2019

Timothy KW

8

1 reference

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14 October 2019

Vincent GM

9

1 reference

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14 October 2019

de Jager T

10

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14 October 2019

Toubin JA

12

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14 October 2019

Moss AJ

13

1 reference

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14 October 2019

Atkinson DL

14

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14 October 2019

Landes GM

15

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14 October 2019

Connors TD

16

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14 October 2019

Keating MT

17

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14 October 2019

language of work or name

English

0 references

publication date

1 January 1996

1 reference

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14 October 2019

1 reference

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14 October 2019

volume

12

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14 October 2019

page(s)

17-23

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14 October 2019

issue

1

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https://scigraph.springernature.com/pub.10.1038/ng0196-17

14 October 2019

exact match

0 references

cites work

Sudden death risk in overt coronary heart disease: the Framingham Study

1 reference

7 January 2021

Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population

1 reference

7 January 2021

Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction

1 reference

7 January 2021

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

7 January 2021

CONGENITAL CARDIAC ARRHYTHMIA

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7 January 2021

The long Q-T syndrome

1 reference

7 January 2021

Unilateral Cervicothoracic Sympathetic Ganglionectomy for the Treatment of Long QT Interval Syndrome

1 reference

7 January 2021

Proarrhythmic effects of antiarrhythmic drugs

1 reference

7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

7 January 2021

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

1 reference

7 January 2021

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

7 January 2021

HERG, a human inward rectifier in the voltage-gated potassium channel family

1 reference

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

7 January 2021

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

1 reference

7 January 2021

Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human

1 reference

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

7 January 2021

Determination of the subunit stoichiometry of a voltage-activated potassium channel

1 reference

7 January 2021

Functional stoichiometry of Shaker potassium channel inactivation.

1 reference

7 January 2021

Shaker, Shal, Shab, and Shaw express independent K+ current systems.

1 reference

7 January 2021

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

1 reference

7 January 2021

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

7 January 2021

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction

1 reference

7 January 2021

Rapid identification of yeast artificial chromosome clones by matrix pooling and crude lysate PCR.

1 reference

7 January 2021

Bacteriophage P1 cloning system for the isolation, amplification, and recovery of DNA fragments as large as 100 kilobase pairs

1 reference

7 January 2021

Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector.

1 reference

7 January 2021

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

1 reference

7 January 2021

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

1 reference

7 January 2021

Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0196-17

2 references

Consolidated OpenCitations Corpus – April 2017

1741279

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528244%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

14 October 2019

1010411062

0 references

1741279

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1741279