(Q36008847)

11 August 2017

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome (English)

1 reference

11 August 2017

1 reference

11

12

object named as

Charles Antzelevitch

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11 August 2017

10

Pedro Brugada

1 reference

11 August 2017

Josep Brugada

9

1 reference

ORCID Public Data File 2021

Ramon Brugada

14

object named as

Ramon Brugada

1 reference

11 August 2017

1

Jonathan M Cordeiro

1 reference

11 August 2017

4

Elena Burashnikov

1 reference

11 August 2017

13

Robert Dumaine

1 reference

11 August 2017

Hector Barajas-Martinez

2

object named as

Hector Barajas-Martinez

1 reference

11 August 2017

Kui Hong

3

1 reference

11 August 2017

Ryan Pfeiffer

5

1 reference

11 August 2017

Anne-Marie Orsino

6

1 reference

11 August 2017

Yue Sheng Wu

7

1 reference

11 August 2017

Dan Hu

8

1 reference

11 August 2017

language of work or name

English

0 references

publication date

30 October 2006

1 reference

11 August 2017

1 reference

11 August 2017

114

1 reference

11 August 2017

19

1 reference

11 August 2017

2026-2033

1 reference

Sodium channels as macromolecular complexes: implications for inherited arrhythmia syndromes

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

A trafficking defective, Brugada syndrome-causing SCN5A mutation rescued by drugs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Currents carried by sodium and potassium ions through the membrane of the giant axon of Loligo

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Proposed diagnostic criteria for the Brugada syndrome: consensus report

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Location of the initiation site of calcium transients and sparks in rabbit heart Purkinje cells

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Cardiac sodium channel and inherited arrhythmia syndromes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Sodium channel selectivity filter regulates antiarrhythmic drug binding

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Functional association of the beta 1 subunit with human cardiac (hH1) and rat skeletal muscle (mu 1) sodium channel alpha subunits expressed in Xenopus oocytes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

A structural model of the tetrodotoxin and saxitoxin binding site of the Na+ channel

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Cardiac Na(+) channel dysfunction in Brugada syndrome is aggravated by beta(1)-subunit.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Molecular basis for pharmacological differences between brain and cardiac sodium channels

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Cellular and ionic basis for the sex-related difference in the manifestation of the Brugada syndrome and progressive conduction disease phenotypes

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989773

Functional expression of GFP-linked human heart sodium channel (hH1) and subcellular localization of the a subunit in HEK293 cells and dog cardiac myocytes

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17075016

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCULATIONAHA.106.627489

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

17075016

1 reference