(Q24302041)

Gap junction protein alpha 5

1 reference

Sodium voltage-gated channel beta subunit 1

1 reference

regulation of atrial cardiac muscle cell membrane depolarization

1 reference

progressive familial heart block

1 reference

21

0 references

Hervé Le Marec

18

0 references

Mario Delmar

22

Mario Delmar

0 references

Arthur Wilde

16

Arthur A M Wilde

0 references

Dan Roden

19

Dan M Roden

0 references

Connie R Bezzina

8

Connie R Bezzina

0 references

Wataru Shimizu

7

Wataru Shimizu

0 references

Minoru Horie

14

Minoru Horie

0 references

Naomasa Makita

1

Naomasa Makita

0 references

Vincent Probst

17

Vincent Probst

0 references

Can Hasdemir

9

Can Hasdemir

0 references

author name string

Akiko Seki

2

0 references

Naokata Sumitomo

3

0 references

Halina Chkourko

4

0 references

Shigetomo Fukuhara

5

0 references

Hiroshi Watanabe

6

0 references

Hideo Mugishima

10

0 references

Takeru Makiyama

11

0 references

Alban Baruteau

12

0 references

Estelle Baron

13

0 references

Nobuhisa Hagiwara

15

0 references

Naoki Mochizuki

Circulation: Arrhythmia and Electrophysiology

20

0 references

language of work or name

English

0 references

publication date

February 2012

0 references

published in

1 reference

Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I

volume

5

0 references

issue

1

0 references

page(s)

163-72

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Cardiac conduction defects associate with mutations in SCN5A

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

The cardiac conduction system

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Paradigm of genetic mosaicism and lone atrial fibrillation: physiological characterization of a connexin 43-deletion mutant identified from atrial tissue

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

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).

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

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=4274644

Sodium channel mutations and arrhythmias

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Structural organization of gap junction channels

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Loss of electrical communication, but not plaque formation, after mutations in the cytoplasmic loop of connexin43.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Translational efficiency of EMCV IRES in bicistronic vectors is dependent upon IRES sequence and gene location

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

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=4274644

Architectural and functional asymmetry of the His-Purkinje system of the murine heart.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

The carboxyl terminal domain regulates the unitary conductance and voltage dependence of connexin40 gap junction channels.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

Gene for progressive familial heart block type I maps to chromosome 19q13.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4274644

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

29 November 2018

1 reference

12 December 2020

The Pathogenesis of Atrioventricular Block in Coronary Disease

1 reference

12 December 2020

An isolated cardiac conduction disease maps to chromosome 19q

1 reference

12 December 2020

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation

1 reference

12 December 2020

10.1161/CIRCEP.111.967604

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

22247482

1 reference