The multifaceted phenotype of the knockout mouse for the KCNE1 potassium channel gene. (Q34520616)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

review article

1 reference

title

The multifaceted phenotype of the knockout mouse for the KCNE1 potassium channel gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

0 references

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

author name string

Jacques Barhanin

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

publication date

1 March 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Physiology - Regulatory, Integrative and Comparative Physiology

6 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

volume

282

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

page(s)

R639-48

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11832382%20AND%20SRC:MED&resulttype=core&format=json

MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

6 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Altered potassium balance and aldosterone secretion in a mouse model of human congenital long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

The protein IsK is a dual activator of K+ and Cl- channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mechanisms of I(Ks) suppression in LQT1 mutants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Role of the ISK protein in the IminK channel complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mice disrupted for the KvLQT1 potassium channel regulator IsK gene accumulate mature T cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Molecular diversity of K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Experimental models of torsade de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Differential expression of Isk mRNAs in mouse tissue during development and pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Cloning and expression of the delayed-rectifier IsK channel from neonatal rat heart and diethylstilbestrol-primed rat uterus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

The cardiac K+ channel KCNQ1 is essential for gastric acid secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

The small conductance K+ channel, KCNQ1: expression, function, and subunit composition in murine trachea

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Distinct gene-specific mechanisms of arrhythmia revealed by cardiac gene transfer of two long QT disease genes, HERG and KCNE1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Functional annotation of a full-length mouse cDNA collection

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Molecular and cellular mechanisms of cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

A new spontaneous mouse mutation in the Kcne1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Characterization of angiotensin II-regulated K+ conductance in rat adrenal glomerulosa cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

A minK-HERG complex regulates the cardiac potassium current I(Kr)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Differential expression of KvLQT1 isoforms across the human ventricular wall

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

The effect of spironolactone on morbidity and mortality in patients with severe heart failure. Randomized Aldactone Evaluation Study Investigators

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Genetic aspects of arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

A practical approach to torsade de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

A constitutively open potassium channel formed by KCNQ1 and KCNE3

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Divalent cations inhibit IsK/KvLQT1 channels in excised membrane patches of strial marginal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Immunohistochemical study of a rat membrane protein which induces a selective potassium permeation: its localization in the apical membrane portion of epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

cAMP increases apical IsK channel current and K+ secretion in vestibular dark cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Mechanism generating endocochlear potential: role played by intermediate cells in stria vascularis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Inner ear defects induced by null mutation of the isk gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Comparison of ion transport mechanisms between vestibular dark cells and strial marginal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Muscarinic receptors control K+ secretion in inner ear strial marginal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001

Voltage-dependent, slowly activating K+ current (I Ks) and its augmentation by carbachol in rat pancreatic acini

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00649.2001