A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y (Q34331339)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16453024%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y (English)

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16 January 2020

9

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16 January 2020

author name string

Leigh D Plant

1

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16 January 2020

Peter N Bowers

2

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16 January 2020

Qianyong Liu

3

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16 January 2020

Thomas Morgan

4

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16 January 2020

Tingting Zhang

5

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16 January 2020

Matthew W State

6

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16 January 2020

Weidong Chen

7

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16 January 2020

Rick A Kittles

8

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16 January 2020

language of work or name

English

0 references

publication date

1 February 2006

1 reference

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Journal of Clinical Investigation

16 January 2020

published in

1 reference

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16 January 2020

volume

116

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16 January 2020

issue

2

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16 January 2020

page(s)

430-435

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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

16 January 2020

cites work

1 reference

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A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia

6 July 2018

1 reference

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Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome

6 July 2018

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Basic Mechanisms of Cardiac Impulse Propagation and Associated Arrhythmias

6 July 2018

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Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

6 July 2018

1 reference

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A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation

6 July 2018

1 reference

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Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

6 July 2018

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Infant mortality statistics from the 2001 period linked birth/infant death data set

6 July 2018

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

6 July 2018

1 reference

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Sleep environment and the risk of sudden infant death syndrome in an urban population: the Chicago Infant Mortality Study

6 July 2018

1 reference

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A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating

6 July 2018

1 reference

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Genetic modifiers of cardiac arrhythmias.

6 July 2018

1 reference

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SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family

6 July 2018

1 reference

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

6 July 2018

1 reference

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

6 July 2018

1 reference

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

6 July 2018

1 reference

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A common polymorphism associated with antibiotic-induced cardiac arrhythmia

6 July 2018

1 reference

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Coexpression with beta(1)-subunit modifies the kinetics and fatty acid block of hH1(alpha) Na(+) channels

6 July 2018

1 reference

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Cardiac conduction defects associate with mutations in SCN5A

6 July 2018

1 reference

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

6 July 2018

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

6 July 2018

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Pharmacological targeting of long QT mutant sodium channels

6 July 2018

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Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

6 July 2018

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Proton block of rat brain sodium channels. Evidence for two proton binding sites and multiple occupancy

6 July 2018

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Cardiorespiratory recordings from infants dying suddenly and unexpectedly at home.

6 July 2018

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

6 July 2018

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Molecular mechanism for an inherited cardiac arrhythmia

6 July 2018

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6 July 2018

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Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development

6 July 2018

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Effects of external protons on single cardiac sodium channels from guinea pig ventricular myocytes

6 July 2018

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In vivo myocardial cell pH in the dog. Response to ischemia and infusion of alkali

6 July 2018

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Intracellular pH and K+ of cardiac and skeletal muscle in acidosis and alkalosis

6 July 2018

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Intracellular proton mobility and buffering power in cardiac ventricular myocytes from rat, rabbit, and guinea pig.

6 July 2018

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Subdiaphragmatic murine electrophysiological studies: sequential determination of ventricular refractoriness and arrhythmia induction

27 October 2018

1 reference

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Intrinsic H(+) ion mobility in the rabbit ventricular myocyte

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1359045

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1359045

An Icelandic example of the impact of population structure on association studies

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1359045

Sudden Cardiac Death, Genes, and Arrhythmogenesis

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16453024

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular diagnosis in a child with sudden infant death syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16453024

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sodium Channel Block With Mexiletine Is Effective in Reducing Dispersion of Repolarization and Preventing Torsade de Pointes in LQT2 and LQT3 Models of the Long-QT Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16453024

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI25618

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16453024%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16453024%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

16453024

1 reference