(Q33608238)

28 July 2017

title

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current (English)

1 reference

sudden infant death syndrome

28 July 2017

main subject

1 reference

Michael J Ackerman

1 reference

28 July 2017

Jianding Cheng

1 reference

28 July 2017

David W Van Norstrand

1 reference

28 July 2017

Argelia Medeiros-Domingo

1 reference

28 July 2017

Carmen Valdivia

1 reference

28 July 2017

Bi-hua Tan

1 reference

28 July 2017

Bin Ye

1 reference

28 July 2017

Stacie Kroboth

1 reference

28 July 2017

Matteo Vatta

1 reference

28 July 2017

David J Tester

1 reference

28 July 2017

Craig T January

1 reference

28 July 2017

Jonathan C Makielski

1 reference

28 July 2017

publication date

1 December 2009

1 reference

Circulation: Arrhythmia and Electrophysiology

28 July 2017

published in

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

28 July 2017

page(s)

667-676

1 reference

alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption

28 July 2017

cites work

1 reference

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21 June 2018

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Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations

21 June 2018

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Cardiac ion channel gene mutations in sudden infant death syndrome

21 June 2018

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Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

21 June 2018

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CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart

21 June 2018

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Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study

21 June 2018

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Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

21 June 2018

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Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study

21 June 2018

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A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors

21 June 2018

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Modulatory effect of NO on sodium currents in a neuroblastoma cell line: aspects of cell specificity.

21 June 2018

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Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

21 June 2018

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21 June 2018

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

21 June 2018

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Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

21 June 2018

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SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene.

21 June 2018

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The sarcolemmal calcium pump, alpha-1 syntrophin, and neuronal nitric-oxide synthase are parts of a macromolecular protein complex

21 June 2018

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A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

21 June 2018

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Sudden infant death syndrome: how significant are the cardiac channelopathies?

21 June 2018

1 reference

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Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 June 2018

1 reference

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A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation

21 June 2018

1 reference

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

21 June 2018

1 reference

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In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4

21 June 2018

1 reference

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Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex

21 June 2018

1 reference

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A molecular link between the sudden infant death syndrome and the long-QT syndrome

21 June 2018

1 reference

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Gab2, a new pleckstrin homology domain-containing adapter protein, acts to uncouple signaling from ERK kinase to Elk-1

21 June 2018

1 reference

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Temperature dependence of early and late currents in human cardiac wild-type and long Q-T DeltaKPQ Na+ channels.

21 June 2018

1 reference

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

21 June 2018

1 reference

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Molecular mechanism for an inherited cardiac arrhythmia

21 June 2018

1 reference

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Mouse α1- and β2-Syntrophin Gene Structure, Chromosome Localization, and Homology with a Discs Large Domain

21 June 2018

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SNP association and sequence analysis of the NOS1AP gene in SIDS.

21 June 2018

1 reference

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What is the mechanism of SIDS? Clues from epidemiology

30 October 2018

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Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration

30 October 2018

1 reference

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Cardiac sodium channel dysfunction in sudden infant death syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Cardiac sodium channel Nav1.5 is regulated by a multiprotein complex composed of syntrophins and dystrophin.

30 October 2018

1 reference

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SIDS--a syndrome in search of a cause

30 October 2018

1 reference

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Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

30 October 2018

1 reference

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Nitric oxide blocks fast, slow, and persistent Na+ channels in C-type DRG neurons by S-nitrosylation

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Nitric oxide modulates cardiac Na(+) channel via protein kinase A and protein kinase G.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Nitric oxide increases persistent sodium current in rat hippocampal neurons

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Prolongation of the QT interval and the sudden infant death syndrome.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810855

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20009079

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sudden infant death syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20009079

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Induction of persistent sodium current by exogenous and endogenous nitric oxide

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20009079

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCEP.109.891440

1 reference

28 July 2017

1 reference

28 July 2017

1 reference