(Q24300388)

Sodium voltage-gated channel alpha subunit 10

GOA release 2020-03-11

1 reference

bundle of His cell action potential

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Charles Antzelevitch

24

0 references

Michel Haïssaguerre

19

0 references

Dan Hu

Dan Hu

1

0 references

Martin Borggrefe

22

Martin Borggrefe

0 references

Rainer Schimpf

21

Rainer Schimpf

0 references

Hector Barajas-Martinez

2

Hector Barajas-Martínez

0 references

Ryan Pfeiffer

3

Ryan Pfeiffer

0 references

Luiz Belardinelli

8

Luiz Belardinelli

0 references

Pramod Deshmukh

14

Pramod Deshmukh

0 references

Mark Marieb

15

Mark Marieb

0 references

Gi Byoung Nam

16

Gi-Byoung Nam

0 references

Christian Veltmann

20

Christian Veltmann

0 references

Sami Viskin

23

Sami Viskin

0 references

Atul Bhatia

17

Atul Bhatia

0 references

author name string

Fabio Dezi

4

0 references

Jenna Pfeiffer

5

0 references

Tapan Buch

6

0 references

Matthew J Betzenhauser

7

0 references

Kristopher M Kahlig

9

0 references

Sridharan Rajamani

10

0 references

Harry J DeAntonio

11

0 references

Robert J Myerburg

12

0 references

Hiroyuki Ito

13

0 references

Can Hasdemir

Journal of the American College of Cardiology

18

0 references

language of work or name

English

0 references

publication date

8 July 2014

0 references

published in

0 references

volume

64

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page(s)

66-79

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issue

1

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cites work

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Genetic variation in SCN10A influences cardiac conduction

19 March 2017

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Brugada syndrome behind complete right bundle-branch block

27 September 2017

1 reference

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Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans

27 September 2017

1 reference

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Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

27 September 2017

1 reference

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Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

27 September 2017

1 reference

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

27 September 2017

1 reference

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Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic

27 September 2017

1 reference

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Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer

27 September 2017

1 reference

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Genetic, molecular and cellular mechanisms underlying the J wave syndromes

27 September 2017

1 reference

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J-wave syndromes. from cell to bedside

27 September 2017

1 reference

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HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

27 September 2017

1 reference

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Genome-wide association studies of the PR interval in African Americans

27 September 2017

1 reference

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Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

27 September 2017

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Genome-wide association study of PR interval

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Brugada syndrome: report of the second consensus conference.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

PN3 sodium channel distribution in the dorsal root ganglia of normal and neuropathic rats

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Several common variants modulate heart rate, PR interval and QRS duration

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Exploring the role of nociceptor-specific sodium channels in pain transmission using Nav1.8 and Nav1.9 knockout mice.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

Structure and function of a novel voltage-gated, tetrodotoxin-resistant sodium channel specific to sensory neurons.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4116276

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24998131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Localisation of SCN10A gene product Na(v)1.8 and novel pain-related ion channels in human heart

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24998131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Functional Nav1.8 channels in intracardiac neurons: the link between SCN10A and cardiac electrophysiology

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24998131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JACC.2014.04.032

1 reference

478880

478880

1 reference

1 reference

1 reference