(Q33533311)

English

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

27 July 2017

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model (English)

1 reference

Europe PubMed Central

27 July 2017

Jean-Jacques Schott

7

object named as

Jean-Jacques Schott

0 references

Flavien Charpentier

18

object named as

Flavien Charpentier

0 references

Hervé Le Marec

13

object named as

Hervé Le Marec

1 reference

Europe PubMed Central

27 July 2017

Solena Le Scouarnec

6

object named as

Solena Le Scouarnec

1 reference

Europe PubMed Central

27 July 2017

object named as

Hugues Abriel

17

0 references

William H. Colledge

object named as

William H Colledge

11

0 references

Patrick Bruneval

9

object named as

Patrick Bruneval

1 reference

Europe PubMed Central

27 July 2017

14

object named as

Arthur A Wilde

1 reference

Europe PubMed Central

27 July 2017

15

object named as

Peter J Mohler

1 reference

Europe PubMed Central

27 July 2017

Sophie Demolombe

8

object named as

Sophie Demolombe

1 reference

Europe PubMed Central

27 July 2017

5

object named as

Vincent Probst

1 reference

Europe PubMed Central

27 July 2017

Céline Marionneau

4

object named as

Céline Marionneau

1 reference

Europe PubMed Central

27 July 2017

author name string

Anne-Laure Leoni

1

1 reference

Europe PubMed Central

27 July 2017

Bruno Gavillet

2

1 reference

Europe PubMed Central

27 July 2017

Jean-Sébastien Rougier

3

1 reference

Europe PubMed Central

27 July 2017

Christopher L H Huang

10

1 reference

Europe PubMed Central

27 July 2017

Andrew A Grace

12

1 reference

Europe PubMed Central

27 July 2017

Denis Escande

16

1 reference

Europe PubMed Central

27 July 2017

language of work or name

0 references

publication date

19 February 2010

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

5

1 reference

Europe PubMed Central

27 July 2017

e9298

1 reference

Europe PubMed Central

27 July 2017

2

1 reference

Europe PubMed Central

27 July 2017

copyright license

Creative Commons Attribution 4.0 International

19 February 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Physiology of cardiovascular gap junctions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Impaired impulse propagation in Scn5a-knockout mice: combined contribution of excitability, connexin expression, and tissue architecture in relation to aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Susceptibility genes and modifiers for cardiac arrhythmias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Mouse model of SCN5A-linked hereditary Lenègre's disease: age-related conduction slowing and myocardial fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Regulation of the voltage-gated cardiac sodium channel Nav1.5 by interacting proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Ankyrin-B targets beta2-spectrin to an intracellular compartment in neonatal cardiomyocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Trafficking and functional expression of cardiac Na+ channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Electrogram prolongation and nifedipine-suppressible ventricular arrhythmias in mice following targeted disruption of KCNE1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Genetic control of sodium channel function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Defective cardiac ion channels: from mutations to clinical syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Cardiac conduction defects associate with mutations in SCN5A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824822

14 July 2018

Abnormal cardiac Na(+) channel properties and QT heart rate adaptation in neonatal ankyrin(B) knockout mice.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0009298

21 January 2018

Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0009298

21 January 2018

Mouse functional genomics requires standardization of mouse handling and housing conditions.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0009298

21 January 2018

Delay in right ventricular activation contributes to Brugada syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0009298

21 January 2018

Aldosterone increases voltage-gated sodium current in ventricular myocytes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0009298

21 January 2018

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20174578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influences of laboratory environment on behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/20174578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20174578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytochemical localization of rH1 sodium channel in adult rat heart atria and ventricle. Presence in terminal intercalated disks

1 reference

https://pubmed.ncbi.nlm.nih.gov/20174578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20174578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0009298

1 reference

Europe PubMed Central

27 July 2017

2010PLoSO...5.9298L

0 references

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33533311&oldid=2084636204"