(Q76385043)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

title

IKs, a slow and intriguing cardiac K+ channel and its associated long QT diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

author name string

J Barhanin

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

B Attali

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

M Lazdunski

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

publication date

1 July 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

Trends in Cardiovascular Medicine

24 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

page(s)

207-214

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

Characterization of two distinct depolarization-activated K+ currents in isolated adult rat ventricular myocytes

24 November 2019

cites work

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A corticosteroid-induced gene expressing an "IsK-like" K+ channel activity in Xenopus oocytes

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Myocardial potassium channels: electrophysiological and molecular diversity

1 reference

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7 January 2021

The minK potassium channel exists in functional and nonfunctional forms when expressed in the plasma membrane of Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Cardiac potassium channels in health and disease

1 reference

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7 January 2021

Role of the ISK protein in the IminK channel complex

1 reference

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7 January 2021

Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B.

1 reference

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7 January 2021

The role of the IsK protein in the specific pharmacological properties of the IKs channel complex

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Molecular physiology of cardiac potassium channels

1 reference

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7 January 2021

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

1 reference

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7 January 2021

KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

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7 January 2021

The inward rectifier potassium channel family.

1 reference

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7 January 2021

TASK, a human background K+ channel to sense external pH variations near physiological pH

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Cloning, functional expression and brain localization of a novel unconventional outward rectifier K+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Suppression of Slow Delayed Rectifier Current by a Truncated Isoform of KvLQT1 Cloned from Normal Human Heart

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Properties and regulation of the minK potassium channel protein

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Evidence for two components of delayed rectifier K+ current in human ventricular myocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

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7 January 2021

Mat-8, a novel phospholemman-like protein expressed in human breast tumors, induces a chloride conductance in Xenopus oocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Outward membrane currents activated in the plateau range of potentials in cardiac Purkinje fibres

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

The cardiac ion channels: relevance to management of arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

CONGENITAL CARDIAC ARRHYTHMIA

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

KVLQT1 mutations in three families with familial or sporadic long QT syndrome

1 reference

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7 January 2021

Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

Dominant-Negative KvLQT1 Mutations Underlie the LQT1 Form of Long QT Syndrome

1 reference

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7 January 2021

Molecular basis of the long-QT syndrome associated with deafness

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

1 reference

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7 January 2021

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene

1 reference

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7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Molecular genetics of long QT syndrome from genes to patients

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2898%2900013-9

7 January 2021

10.1016/S1050-1738(98)00013-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14987566%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

1 reference