(Q33148552)

22 July 2017

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation (English)

1 reference

22 July 2017

Prakash C Viswanathan

series ordinal

1

1 reference

22 July 2017

D Woodrow Benson

series ordinal

2

1 reference

22 July 2017

Jeffrey R Balser

series ordinal

3

1 reference

22 July 2017

language of work or name

English

0 references

publication date

1 February 2003

1 reference

Journal of Clinical Investigation

22 July 2017

1 reference

22 July 2017

111

1 reference

22 July 2017

3

1 reference

22 July 2017

341-346

1 reference

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

22 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Differential distribution of cardiac ion channel expression as a basis for regional specialization in electrical function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

The heart SNPs a beat: polymorphisms in candidate genes for cardiovascular disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

A sodium-channel mutation causes isolated cardiac conduction disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Genetic susceptibility to cardiovascular diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

The role of apolipoprotein E in Alzheimer's disease: pharmacogenomic target selection

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Pharmacogenetics and the practice of medicine

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

"Brugada" syndrome: clinical data and suggested pathophysiological mechanism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Pharmacogenetics and the treatment of cardiovascular disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Apolipoprotein E and Alzheimer's disease. The tip of the susceptibility iceberg.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Autoimmune-associated congenital heart block: demographics, mortality, morbidity and recurrence rates obtained from a national neonatal lupus registry

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=151865

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12569159

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Low penetrance in the long-QT syndrome: clinical impact

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12569159

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12569159

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI200316879

1 reference

22 July 2017

1 reference

22 July 2017

1 reference