Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A (Q24337302)

Sodium voltage-gated channel beta subunit 3

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

8

Charles Antzelevitch

Charles

Antzelevitch

1 reference

20 October 2023

Ryan Pfeiffer

4

Ryan

Pfeiffer

1 reference

20 October 2023

Soren Grubb

3

Soren

Grubb

1 reference

20 October 2023

Kirstine Calloe

1

Kirstine

Calloe

1 reference

20 October 2023

Nicole Schmitt

2

Nicole

Schmitt

1 reference

20 October 2023

Jens-Peter David

5

Jens-Peter

David

1 reference

20 October 2023

Ronald Kanter

series ordinal

6

author given names

Ronald

author last names

Kanter

1 reference

20 October 2023

Jonathan M Cordeiro

series ordinal

7

author given names

Jonathan M

author last names

Cordeiro

1 reference

Canadian Journal of Physiology and Pharmacology

20 October 2023

language of work or name

English

0 references

publication date

October 2011

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published in

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volume

89

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issue

10

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page(s)

723-36

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cites work

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Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3.

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A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

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Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome

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Augmentation of late sodium current unmasks the proarrhythmic effects of amiodarone.

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27 September 2017

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Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation

30 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208331

Molecular determinants of beta 1 subunit-induced gating modulation in voltage-dependent Na+ channels.

30 May 2018

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30 May 2018

1 reference

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Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

30 May 2018

1 reference

A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation

21 January 2018

1 reference

Multiple mechanisms of Na+ channel--linked long-QT syndrome

21 January 2018

1 reference

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

21 January 2018

1 reference

Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes

21 January 2018

1 reference

The extracellular domain of the beta1 subunit is both necessary and sufficient for beta1-like modulation of sodium channel gating

21 January 2018

1 reference

Cardiac memory evolves with age in association with development of the transient outward current.

21 January 2018

1 reference

Modulation of cardiac Na+ channel expression in Xenopus oocytes by beta 1 subunits

21 January 2018

1 reference

Thyroid hormone regulates postnatal expression of transient K+ channel isoforms in rat ventricle.

21 January 2018

1 reference

Antagonism by ranolazine of the pro-arrhythmic effects of increasing late INa in guinea pig ventricular myocytes

21 January 2018

1 reference

Postnatal development of atrial repolarization in the mouse.

21 January 2018

1 reference

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine

21 January 2018

1 reference

Cardiac sodium channel dysfunction in sudden infant death syndrome.

21 January 2018

1 reference

Amiodarone-associated macroscopic T-wave alternans and torsade de pointes unmasking the inherited long QT syndrome

21 January 2018

1 reference

Antiarrhythmic effects of ranolazine in a guinea pig in vitro model of long-QT syndrome

21 January 2018

1 reference

The sodium channel -subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart

21 January 2018

1 reference

Guidelines for the interpretation of the neonatal electrocardiogram

21 January 2018

1 reference

Brugada syndrome and sudden cardiac death in children

21 January 2018

1 reference

12 December 2020

Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel

1 reference

12 December 2020

A critical role for transmembrane segment IVS6 of the sodium channel alpha subunit in fast inactivation

1 reference

12 December 2020

Divergent action potential morphologies reveal nonequilibrium properties of human cardiac Na channels

1 reference

12 December 2020

Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood

1 reference

12 December 2020

Genetic modulation of cardiac repolarization reserve

1 reference

12 December 2020

release_ohzoyqxhsjgyvev2otov7ymdvm

Identifiers

DOI

10.1139/Y11-070

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Fatcat ID

0 references

PMC publication ID

3208331

0 references