(Q33161467)

23 July 2017

title

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits (English)

1 reference

23 July 2017

Nathalie Neyroud

11

0 references

Stéphane Hatem

object named as

Stéphane N Hatem

7

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Pascale Guicheney

object named as

Pascale Guicheney

10

0 references

author name string

Jérôme Clatot

1

1 reference

23 July 2017

Azza Ziyadeh-Isleem

2

1 reference

23 July 2017

Svetlana Maugenre

3

1 reference

23 July 2017

Isabelle Denjoy

4

1 reference

23 July 2017

Haiyan Liu

5

1 reference

23 July 2017

Gilles Dilanian

6

1 reference

23 July 2017

Isabelle Deschênes

8

1 reference

23 July 2017

Alain Coulombe

9

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23 July 2017

publication date

27 June 2012

1 reference

23 July 2017

published in

Cardiovascular Research

1 reference

23 July 2017

volume

96

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23 July 2017

issue

1

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23 July 2017

page(s)

53-63

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describes a project that uses

23 July 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3444234/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3444234

Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome

28 July 2018

1 reference

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Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology

28 July 2018

1 reference

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The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking

28 July 2018

1 reference

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Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channel

28 July 2018

1 reference

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Post-transcriptional gene silencing of KChIP2 and Navbeta1 in neonatal rat cardiac myocytes reveals a functional association between Na and Ito currents

28 July 2018

1 reference

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A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels.

28 July 2018

1 reference

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Tipping the delicate balance: defining how proteasome maturation affects the degradation of a substrate for autophagy and endoplasmic reticulum associated degradation (ERAD).

28 July 2018

1 reference

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

28 July 2018

1 reference

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Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

28 July 2018

1 reference

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

28 July 2018

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Pharmacologic rescue of conformationally-defective proteins: implications for the treatment of human disease

28 July 2018

1 reference

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

28 July 2018

1 reference

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Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

28 July 2018

1 reference

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Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

28 July 2018

1 reference

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Inward sodium current at resting potentials in single cardiac myocytes induced by the ischemic metabolite lysophosphatidylcholine

28 July 2018

1 reference

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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

28 July 2018

1 reference

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Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac sodium channel

21 January 2018

1 reference

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In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant

21 January 2018

1 reference

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MOG1: a new susceptibility gene for Brugada syndrome.

21 January 2018

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Rescuing cystic fibrosis transmembrane conductance regulator (CFTR)-processing mutants by transcomplementation

21 January 2018

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Rescue of functional DeltaF508-CFTR channels by co-expression with truncated CFTR constructs in COS-1 cells

21 January 2018

1 reference

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Functional complementation of Glra1(spd-ot), a glycine receptor subunit mutant, by independently expressed C-terminal domains.

21 January 2018

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Role of the amino and carboxy termini in isoform-specific sodium channel variation

21 January 2018

1 reference

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Sick Sinus Syndrome, Progressive Cardiac Conduction Disease, Atrial Flutter and Ventricular Tachycardia Caused by a Novel SCN5A Mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVS211

21 January 2018

Identifiers

DOI

10.1093/CVR/CVS211

1 reference

23 July 2017

1 reference

23 July 2017

1 reference