(Q44018910)

29 November 2017

title

A truncated splice variant of KCNQ1 cloned from rat heart (English)

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29 November 2017

Yoichi Yamada

1

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29 November 2017

Xiangdong Chen

2

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29 November 2017

Takeshi Kobayashi

3

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29 November 2017

Yasuhiro Kamada

4

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29 November 2017

Masato Nagashima

5

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29 November 2017

Masaaki Tsutsuura

6

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29 November 2017

Sumihiko Seki

7

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29 November 2017

Michiaki Yamakage

8

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29 November 2017

Akiyoshi Namiki

9

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29 November 2017

Noritsugu Tohse

10

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29 November 2017

language of work or name

English

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publication date

1 June 2002

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Biochemical and Biophysical Research Communications

29 November 2017

published in

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29 November 2017

volume

294

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29 November 2017

issue

2

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29 November 2017

page(s)

199-204

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

29 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900459-X

Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis

7 January 2021

1 reference

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Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

7 January 2021

1 reference

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

7 January 2021

1 reference

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Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

7 January 2021

1 reference

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K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900459-X

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900459-X

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

7 January 2021

1 reference

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Genetic manipulation of cardiac K(+) channel function in mice: what have we learned, and where do we go from here?

7 January 2021

1 reference

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Mechanisms of I(Ks) suppression in LQT1 mutants.

7 January 2021

1 reference

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

7 January 2021

1 reference

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Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.

7 January 2021

1 reference

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Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

7 January 2021

1 reference

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Cloning and function of the rat colonic epithelial K+ channel KVLQT1

7 January 2021

1 reference

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A constitutively open potassium channel formed by KCNQ1 and KCNE3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900459-X

Colocalization of KCNQ1/KCNE channel subunits in the mouse gastrointestinal tract

7 January 2021

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A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

7 January 2021

1 reference

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Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart

7 January 2021

1 reference

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Unitary current through the inward rectifier K+ channel cloned from rabbit heart--comparison with the native K+ channel.

7 January 2021

1 reference

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Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice.

7 January 2021

1 reference

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Developmental changes in the delayed rectifier K+ channels in mouse heart.

7 January 2021

1 reference

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Four kinetically distinct depolarization-activated K+ currents in adult mouse ventricular myocytes

7 January 2021

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Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

7 January 2021

1 reference

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Functional consequences of the arrhythmogenic G306R KvLQT1 K+ channel mutant probed by viral gene transfer in cardiomyocytes

7 January 2021

1 reference

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Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900459-X

Differential expression of voltage-gated K+ channel subunits in adult rat heart. Relation to functional K+ channels?

7 January 2021

1 reference

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Quantitative analysis of potassium channel mRNA expression in atrial and ventricular muscle of rats

7 January 2021

1 reference

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Heterogeneity of Kv2.1 mRNA expression and delayed rectifier current in single isolated myocytes from rat left ventricle

7 January 2021

1 reference

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

7 January 2021

1 reference

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10.1016/S0006-291X(02)00459-X

7 January 2021

Identifiers

DOI

1 reference

29 November 2017

1 reference