Neuronal KCNQ potassium channels: physiology and role in disease. (Q34185467)

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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

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31 July 2017

language of work or name

English

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publication date

1 October 2000

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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

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5 November 2019

volume

1

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5 November 2019

issue

1

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5 November 2019

page(s)

21-30

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

5 November 2019

exact match

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cites work

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

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

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

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

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

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

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Inner ear defects induced by null mutation of the isk gene

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A constitutively open potassium channel formed by KCNQ1 and KCNE3

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

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

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

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Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability

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

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

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

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Ion channel defects in cardiac arrhythmia

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

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

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

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

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

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

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Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channels

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

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

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

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The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy

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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.

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

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

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

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

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

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The new voltage gated potassium channel KCNQ5 and neonatal convulsions

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

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

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

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KCNE1 mutations cause jervell and Lange-Nielsen syndrome

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

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

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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

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

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Synaptic mechanisms for coding timing in auditory neurons

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

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

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7 January 2021

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

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

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7 January 2021

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

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

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

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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

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7 January 2021

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

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7 January 2021

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

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Mechanoelectrical transduction by hair cells.

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Prestin is the motor protein of cochlear outer hair cells

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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

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1 reference