Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
(Q34185467)
Watch
English
Neuronal KCNQ potassium channels: physiology and role in disease.
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Neuronal KCNQ potassium channels: physiology and role in disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
main subject
potassium
0 references
physiology
0 references
author
Thomas Jentsch
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
author name string
Jentsch TJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
retrieved
31 July 2017
language of work or name
English
0 references
publication date
1 October 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
published in
Nature Reviews Neuroscience
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
21-30
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
cites work
Neurobiology of the Caenorhabditis elegans genome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Voltage-gated ion channels and hereditary disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A potassium channel mutation in neonatal human epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inner ear defects induced by null mutation of the isk gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A constitutively open potassium channel formed by KCNQ1 and KCNE3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ion channel defects in cardiac arrhythmia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndromes and torsade de pointes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The LQT syndromes--current status of molecular mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of the epilepsies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ion channels and epilepsy in man and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seizure characteristics in chromosome 20 benign familial neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Control of M-current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of a cognition-enhancer, linopirdine (DuP 996), on M-type potassium currents (IK(M)) and some other voltage- and ligand-gated membrane currents in rat sympathetic neurons.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antagonistic adrenergic-muscarinic regulation of M current in smooth muscle cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Separation of M-like current and ERG current in NG108-15 cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The new voltage gated potassium channel KCNQ5 and neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNE1 mutations cause jervell and Lange-Nielsen syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of absence of cochlear outer hair cells on behavioural auditory threshold
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of the gap-junction connexins 26 and 30 in the rat cochlea
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ionic properties of IK,n in outer hair cells of guinea pig cochlea
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping the distribution of outer hair cell voltage-dependent conductances by electrical amputation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental expression of the potassium current IK,n contributes to maturation of mouse outer hair cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Major potassium conductance in type I hair cells from rat semicircular canals: characterization and modulation by nitric oxide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synaptic mechanisms for coding timing in auditory neurons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recessive variant of the Romano-Ward long-QT syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the mechanism of M-current inhibition by muscarinic m1 receptors in DNA-transfected rodent neuroblastoma x glioma cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice lacking the basolateral Na-K-2Cl cotransporter have impaired epithelial chloride secretion and are profoundly deaf
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanoelectrical transduction by hair cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prestin is the motor protein of cochlear outer hair cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35036198
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/35036198
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
Dimensions Publication ID
1032891412
0 references
PubMed publication ID
11252765
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11252765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
ResearchGate publication ID
12079294
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit