(Q24534117)

4 July 2017

0 references

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation (English)

1 reference

familial atrial fibrillation

4 July 2017

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0 references

1 reference

Yiqing Yang

1

1 reference

4 July 2017

Min Xia

2

1 reference

4 July 2017

Qingfeng Jin

3

1 reference

4 July 2017

Saïd Bendahhou

4

1 reference

4 July 2017

Jingyi Shi

5

1 reference

4 July 2017

Yiping Chen

6

1 reference

4 July 2017

Bo Liang

7

1 reference

4 July 2017

Jie Lin

8

1 reference

4 July 2017

Yi Liu

9

1 reference

4 July 2017

Ban Liu

10

1 reference

4 July 2017

Qinshu Zhou

11

1 reference

4 July 2017

Dongwei Zhang

12

1 reference

4 July 2017

Rong Wang

13

1 reference

4 July 2017

Ning Ma

14

1 reference

4 July 2017

Xiaoyan Su

15

1 reference

4 July 2017

Kaiya Niu

16

1 reference

4 July 2017

Yan Pei

17

1 reference

4 July 2017

Wenyuan Xu

18

1 reference

4 July 2017

Zhaopeng Chen

19

1 reference

4 July 2017

Haiying Wan

20

1 reference

4 July 2017

Jianmin Cui

21

1 reference

4 July 2017

Jacques Barhanin

22

1 reference

4 July 2017

Yihan Chen

23

1 reference

4 July 2017

language of work or name

English

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publication date

13 September 2004

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

75

1 reference

4 July 2017

issue

5

1 reference

4 July 2017

page(s)

899-905

1 reference

Observations on the Inception of the Rhythm of the Heart by the Ventricle: As the cause of Continuous Irregularity of the Heart

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

KCNQ1 gain-of-function mutation in familial atrial fibrillation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Familial atrial fibrillation is a genetically heterogeneous disorder.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

New ideas about atrial fibrillation 50 years on.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Epidemiology and natural history of atrial fibrillation: clinical implications

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

The long QT syndromes: genetic basis and clinical implications

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Molecular basis of electrical remodeling in atrial fibrillation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Basic mechanisms of atrial fibrillation--very new insights into very old ideas

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Epidemiology and significance of atrial fibrillation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Atrial electrophysiological remodeling caused by rapid atrial activation: underlying mechanisms and clinical relevance to atrial fibrillation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT 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=1182120

Identification of a genetic locus for familial atrial fibrillation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Effects of selective vagal and stellate ganglion stimulation of atrial refractoriness.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

Mutant MiRP1 subunits modulate HERG K+ channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182120

A focal source of atrial fibrillation treated by discrete radiofrequency ablation

29 November 2018

1 reference

12 December 2020

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

1 reference

12 December 2020

Differing sympathetic and vagal effects on atrial fibrillation in dogs: role of refractoriness heterogeneity

1 reference

12 December 2020

Locus for atrial fibrillation maps to chromosome 6q14-16

1 reference

12 December 2020

Initiation of atrial fibrillation by ectopic beats originating from the pulmonary veins: electrophysiological characteristics, pharmacological responses, and effects of radiofrequency ablation

1 reference

12 December 2020

Identifiers

DOI

10.1086/425342

1 reference

OpenCitations bibliographic resource ID

4 July 2017

2835764

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference