(Q34185467)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

review article

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title

Neuronal KCNQ potassium channels: physiology and role in disease (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

Jentsch TJ

series ordinal

1

1 reference

31 July 2017

language of work or name

English

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publication date

1 October 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

Nature Reviews Neuroscience

5 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

21-30

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/35036198

5 November 2019

exact match

0 references

cites work

Neurobiology of the Caenorhabditis elegans genome.

1 reference

7 January 2021

Voltage-gated ion channels and hereditary disease

1 reference

7 January 2021

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

1 reference

7 January 2021

A potassium channel mutation in neonatal human epilepsy

1 reference

7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1 reference

7 January 2021

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

7 January 2021

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

1 reference

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

7 January 2021

A constitutively open potassium channel formed by KCNQ1 and KCNE3

1 reference

7 January 2021

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

1 reference

7 January 2021

Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone

1 reference

7 January 2021

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

1 reference

7 January 2021

Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability

1 reference

7 January 2021

KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents

1 reference

7 January 2021

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity

1 reference

7 January 2021

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

1 reference

7 January 2021

Ion channel defects in cardiac arrhythmia

1 reference

7 January 2021

Long QT syndromes and torsade de pointes

1 reference

7 January 2021

The LQT syndromes--current status of molecular mechanisms

1 reference

7 January 2021

Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium

1 reference

7 January 2021

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy

1 reference

7 January 2021

A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly

1 reference

7 January 2021

The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3

1 reference

7 January 2021

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

1 reference

7 January 2021

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy

1 reference

7 January 2021

Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channels

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetics of the epilepsies

1 reference

7 January 2021

Ion channels and epilepsy in man and mouse

1 reference

7 January 2021

Seizure characteristics in chromosome 20 benign familial neonatal convulsions

1 reference

7 January 2021

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

1 reference

7 January 2021

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

1 reference

7 January 2021

A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family

1 reference

7 January 2021

A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions

1 reference

7 January 2021

The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy

1 reference

7 January 2021

1 reference

7 January 2021

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

7 January 2021

Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current

1 reference

7 January 2021

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

1 reference

7 January 2021

Antagonistic adrenergic-muscarinic regulation of M current in smooth muscle cells

1 reference

7 January 2021

The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits

1 reference

7 January 2021

Separation of M-like current and ERG current in NG108-15 cells

1 reference

7 January 2021

The new voltage gated potassium channel KCNQ5 and neonatal convulsions

1 reference

7 January 2021

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

1 reference

7 January 2021

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

1 reference

7 January 2021

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

1 reference

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

Effect of absence of cochlear outer hair cells on behavioural auditory threshold

1 reference

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

7 January 2021

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

7 January 2021

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

1 reference

7 January 2021

Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)

1 reference

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

7 January 2021

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

1 reference

7 January 2021

Ionic properties of IK,n in outer hair cells of guinea pig cochlea

1 reference

7 January 2021

Mapping the distribution of outer hair cell voltage-dependent conductances by electrical amputation

1 reference

7 January 2021

Developmental expression of the potassium current IK,n contributes to maturation of mouse outer hair cells.

1 reference

7 January 2021

Major potassium conductance in type I hair cells from rat semicircular canals: characterization and modulation by nitric oxide

1 reference

7 January 2021

Synaptic mechanisms for coding timing in auditory neurons

1 reference

7 January 2021

A recessive variant of the Romano-Ward long-QT syndrome?

1 reference

7 January 2021

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

1 reference

7 January 2021

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk

1 reference

7 January 2021

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

On the mechanism of M-current inhibition by muscarinic m1 receptors in DNA-transfected rodent neuroblastoma x glioma cells.

1 reference

7 January 2021

Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis.

1 reference

7 January 2021

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

1 reference

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

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Mechanoelectrical transduction by hair cells.

1 reference

7 January 2021

Prestin is the motor protein of cochlear outer hair cells

1 reference

7 January 2021

Identifiers

DOI

10.1038/35036198

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252765%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 November 2019

0 references

1 reference