(Q46475665)

English

A novel missense mutation in the SCN5A gene associated with Brugada syndrome bidirectionally affecting blocking actions of antiarrhythmic drugs

scientific article published in May 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

A novel missense mutation in the SCN5A gene associated with Brugada syndrome bidirectionally affecting blocking actions of antiarrhythmic drugs (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Brugada syndrome

1 reference

based on heuristic

inferred from title

author name string

Hideki Itoh

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Masami Shimizu

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Shigeo Takata

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Hiroshi Mabuchi

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Keiji Imoto

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

publication date

1 May 2005

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Journal of Cardiovascular Electrophysiology

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

16

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

486-493

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Novel mutations in domain I of SCN5A cause Brugada syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Proposed diagnostic criteria for the Brugada syndrome: consensus report

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Single point mutations affect fatty acid block of human myocardial sodium channel alpha subunit Na+ channels

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Natural history of Brugada syndrome: insights for risk stratification and management

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Role of amino acid residues in transmembrane segments IS6 and IIS6 of the Na+ channel alpha subunit in voltage-dependent gating and drug block.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40711.X

21 January 2018

Identifiers

10.1111/J.1540-8167.2005.40711.X

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15877619

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