(Q52560775)

3 May 2018

title

Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans. (English)

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3 May 2018

author

Ebenezer N. Yamoah

3

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author name string

Mathew C Casimiro

1

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3 May 2018

Bjoern C Knollmann

2

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3 May 2018

Liping Nie

4

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3 May 2018

Jay C Vary

5

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3 May 2018

Syevda G Sirenko

6

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3 May 2018

Anne E Greene

7

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3 May 2018

Alexander Grinberg

8

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3 May 2018

Sing Ping Huang

9

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3 May 2018

Steven N Ebert

10

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3 May 2018

Karl Pfeifer

11

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3 May 2018

publication date

1 September 2004

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3 May 2018

published in

Genomics

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3 May 2018

volume

84

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3 May 2018

issue

3

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3 May 2018

page(s)

555-564

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3 May 2018

Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Molecular and cellular mechanisms of cardiac arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNE regulation of KvLQT1 channels: structure-function correlates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Cloning of a membrane protein that induces a slow voltage-gated potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

A constitutively open potassium channel formed by KCNQ1 and KCNE3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNE4 is an inhibitory subunit to the KCNQ1 channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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%2FJ.YGENO.2004.06.007

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%2FJ.YGENO.2004.06.007

Slowly activating voltage-dependent K+ conductance is apical pathway for K+ secretion in vestibular dark cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Molecular basis of the long-QT syndrome associated with deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Pathology of the ear in the cardio-auditory syndrome of Jervell and Lange-Nielsen. Report of a third case with an appendix on possible linkage with the Rh blood group locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

K(+)-induced stimulation of K+ secretion involves activation of the IsK channel in vestibular dark cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Inner ear defects induced by null mutation of the isk gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Isoproterenol exacerbates a long QT phenotype in Kcnq1-deficient neonatal mice: possible roles for human-like Kcnq1 isoform 1 and slow delayed rectifier K+ current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Nicotine induces a long QT phenotype in Kcnq1-deficient mouse hearts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Functional effects of mutations in KvLQT1 that cause long QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Effect of subadipose tissue on the variables of signal-averaged electrocardiography in healthy subjects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNQ1 gain-of-function mutation in familial atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Prolonged Atrial Action Potential Durations and Polymorphic Atrial Tachyarrhythmias in Patients with Long QT Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Developmental changes in ionic channel activity in the embryonic murine heart

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Divergent expression of delayed rectifier K+ channel subunits during mouse heart development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Involvement of IsK-associated K+ channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Imprinting of mouse Kvlqt1 is developmentally regulated.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Site-directed mutagenesis of virtually any plasmid by eliminating a unique site

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Efficient in vivo manipulation of mouse genomic sequences at the zygote stage

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Mice lacking the basolateral Na-K-2Cl cotransporter have impaired epithelial chloride secretion and are profoundly deaf.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.06.007

10.1016/J.YGENO.2004.06.007

7 January 2021

Identifiers

DOI

1 reference

3 May 2018

1 reference

3 May 2018