Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome (Q24655604)

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19 January 2020

title

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome (English)

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19 January 2020

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13

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19 January 2020

Eva Delpón

1

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19 January 2020

Lucía Nuñez

3

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19 January 2020

Jorgen K. Kanters

8

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19 January 2020

Charles Antzelevitch

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19 January 2020

author name string

Jonathan M Cordeiro

2

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19 January 2020

Poul Erik Bloch Thomsen

4

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19 January 2020

Alejandra Guerchicoff

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19 January 2020

Guido D Pollevick

6

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19 January 2020

Yuesheng Wu

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19 January 2020

Carsten Toftager Larsen

9

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19 January 2020

Jacob Hofman-Bang

10

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19 January 2020

Elena Burashnikov

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19 January 2020

Michael Christiansen

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19 January 2020

language of work or name

English

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publication date

1 August 2008

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Circulation: Arrhythmia and Electrophysiology

19 January 2020

published in

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19 January 2020

volume

1

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19 January 2020

issue

3

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19 January 2020

page(s)

209-218

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Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

19 January 2020

cites work

1 reference

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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

7 April 2017

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Expression and function of dipeptidyl-aminopeptidase-like protein 6 as a putative beta-subunit of human cardiac transient outward current encoded by Kv4.3

7 April 2017

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Functional modulation of the transient outward current Ito by KCNE beta-subunits and regional distribution in human non-failing and failing hearts

7 April 2017

1 reference

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KCNE3 is an inhibitory subunit of the Kv4.3 potassium channel

7 April 2017

1 reference

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Regulation of Kv4.3 current by KChIP2 splice variants: a component of native cardiac I(to)?

7 April 2017

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

7 April 2017

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The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient

7 April 2017

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Association of 14-3-3 proteins to beta1-adrenergic receptors modulates Kv11.1 K+ channel activity in recombinant systems.

7 April 2017

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In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

28 September 2017

1 reference

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Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).

28 September 2017

1 reference

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Does KCNE5 play a role in long QT syndrome?

28 September 2017

1 reference

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Pharmacology of cardiac potassium channels.

28 September 2017

1 reference

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Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

28 September 2017

1 reference

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Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation

28 September 2017

1 reference

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The calcium-independent transient outward potassium current in isolated ferret right ventricular myocytes. I. Basic characterization and kinetic analysis

28 September 2017

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Transient outward current prominent in canine ventricular epicardium but not endocardium

28 September 2017

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

28 September 2017

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Role of sodium and calcium channel block in unmasking the Brugada syndrome

28 September 2017

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Regional variations in action potentials and transient outward current in myocytes isolated from rabbit left ventricle

30 May 2018

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NFATc3-induced reductions in voltage-gated K+ currents after myocardial infarction

30 May 2018

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Cellular and ionic basis for the sex-related difference in the manifestation of the Brugada syndrome and progressive conduction disease phenotypes

28 November 2018

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Concordant expression of KChIP2 mRNA, protein and transient outward current throughout the canine ventricle

28 November 2018

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Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

28 November 2018

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Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome

28 November 2018

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Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

28 November 2018

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Role of the Kv4.3 K+ channel in ventricular muscle. A molecular correlate for the transient outward current

28 November 2018

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aVR sign as a risk factor for life-threatening arrhythmic events in patients with Brugada syndrome

28 November 2018

1 reference

12 December 2020

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12 December 2020

Heterogeneity of action potential waveforms and potassium currents in rat ventricle

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12 December 2020

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12 December 2020

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

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12 December 2020

The Brugada Syndrome: From Bench to Bedside

1 reference

Crossref

https://api.crossref.org/works/10.1161%2FCIRCEP.107.748103

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1161/CIRCEP.107.748103

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122847%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

2 references

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19 January 2020

PubMed publication ID

19122847

2 references