(Q24299782)

Potassium voltage-gated channel subfamily D member 3

1 reference

Potassium voltage-gated channel interacting protein 2

1 reference

A-type (transient outward) potassium channel activity

1 reference

ventricular fibrillation

1 reference

Seiko Ohno

1

0 references

Dimitar P Zankov

2

0 references

Wei-Guang Ding

3

0 references

Hideki Itoh

4

0 references

Takeru Makiyama

5

0 references

Takahiro Doi

6

0 references

Satoshi Shizuta

7

0 references

Tetsuhisa Hattori

8

0 references

Akashi Miyamoto

9

0 references

Nobu Naiki

10

0 references

Jules C Hancox

11

0 references

Hiroshi Matsuura

12

0 references

Minoru Horie

Circulation: Arrhythmia and Electrophysiology

13

0 references

language of work or name

English

0 references

publication date

June 2011

0 references

published in

1 reference

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome

PubMed

volume

4

0 references

issue

3

0 references

page(s)

352-61

0 references

cites work

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Functional modulation of the transient outward current Ito by KCNE beta-subunits and regional distribution in human non-failing and failing hearts

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Does KCNE5 play a role in long QT syndrome?

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutations

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Gender differences in clinical manifestations of Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Cellular consequences of HERG mutations in the long QT syndrome: precursors to sudden cardiac death

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

hKChIP2 is a functional modifier of hKv4.3 potassium channels: cloning and expression of a short hKChIP2 splice variant

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Modulation of A-type potassium channels by a family of calcium sensors

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

X-inactivation profile reveals extensive variability in X-linked gene expression in females

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Cellular and ionic mechanisms responsible for the Brugada syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

A transient outward potassium current activator recapitulates the electrocardiographic manifestations of Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Transient outward potassium current, 'Ito', phenotypes in the mammalian left ventricle: underlying molecular, cellular and biophysical mechanisms

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCEP.110.959619

7 January 2021

10.1161/CIRCEP.110.959619

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

21493962

1 reference

Consolidated OpenCitations Corpus – April 2017