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

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

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

http://www.wikidata.org/entity/Q24651211

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Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity Structural insight into KCNQ (Kv7) channel assembly and channelopathy Neural KCNQ (Kv7) channels Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy Driving with no brakes: molecular pathophysiology of Kv7 potassium channels Dynamic formation of ER-PM junctions presents a lipid phosphatase to regulate phosphoinositides KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents Functional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytes The acrylamide (S)-2 as a positive and negative modulator of Kv7 channels expressed in Xenopus laevis oocytes Focal aggregation of voltage-gated, Kv2.1 subunit-containing, potassium channels at synaptic sites in rat spinal motoneurones AKAP150 signaling complex promotes suppression of the M-current by muscarinic agonists Regulation of KCNQ/Kv7 family voltage-gated K+ channels by lipids.Central cholinesterase inhibition enhances glutamatergic synaptic transmission.Muscarinic acetylcholine receptor subtype expression in avian vestibular hair cells, nerve terminals and ganglion cells Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents.KCNQ-like potassium channels in Caenorhabditis elegans. Conserved properties and modulation.Effects of KCNQ channel blockers on K(+) currents in vestibular hair cells.Electrophysiological properties of human induced pluripotent stem cells.Novel Kv7.1-phosphatidylinositol 4,5-bisphosphate interaction sites uncovered by charge neutralization scanning Electrolyte transport in the mammalian colon: mechanisms and implications for disease.Computational modeling reveals key contributions of KCNQ and hERG currents to the malleability of uterine action potentials underpinning labor.Effects of KCNQ2 gene truncation on M-type Kv7 potassium currents Coupling of the nucleotide P2Y4 receptor to neuronal ion channels Contributions of Kv7-mediated potassium current to sub- and suprathreshold responses of rat layer II/III neocortical pyramidal neurons.Excitatory muscarinic modulation strengthens virtual nicotinic synapses on sympathetic neurons and thereby enhances synaptic gain Electrostatic interaction of internal Mg2+ with membrane PIP2 Seen with KCNQ K+ channels.Calmodulin mediates Ca2+-dependent modulation of M-type K+ channels Novel Roles for Kv7 Channels in Shaping Histamine-Induced Contractions and Bradykinin-Dependent Relaxations in Pig Coronary Arteries.The Sensorless Pore Module of Voltage-gated K+ Channel Family 7 Embodies the Target Site for the Anticonvulsant Retigabine.Ethanol inhibition of m-current and ethanol-induced direct excitation of ventral tegmental area dopamine neurons.Efferent actions in the chinchilla vestibular labyrinth PKC activation and PIP(2) depletion underlie biphasic regulation of IKs by Gq-coupled receptors.Differential gene expression in the salivary gland during development and onset of xerostomia in Sjögren's syndrome-like disease of the C57BL/6.NOD-Aec1Aec2 mouse.Affinity for phosphatidylinositol 4,5-bisphosphate determines muscarinic agonist sensitivity of Kv7 K+ channels.Nicotinic acetylcholine receptors regulate vestibular afferent gain and activation timing.Chansporter complexes in cell signaling.Massive Ca-induced membrane fusion and phospholipid changes triggered by reverse Na/Ca exchange in BHK fibroblasts.Interaction with AKAP79 modifies the cellular pharmacology of PKC.Dual control of cardiac Na+ Ca2+ exchange by PIP(2): electrophysiological analysis of direct and indirect mechanisms.Differential receptor activation by cockroach adipokinetic hormones produces differential effects on ion currents, neuronal activity, and locomotion.

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P2860

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

http://www.wikidata.org/entity/Q24651211

description

2000 nî lūn-bûn

@nan

2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի փետրվարին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

@ast

Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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type

label

Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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prefLabel

Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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J.1469-7793.2000.T01-2-00349.X

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The Journal of Physiology

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Inhibition of KCNQ1-4 potassiu ...... arinic acetylcholine receptors

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A A Selyanko

http://www.w3.org/2001/XMLSchema#string

D A Brown

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F C Abogadie

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J K Hadley

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P2860

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

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

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

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

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

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

A potassium channel mutation in neonatal human epilepsy

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

Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell

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

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349-355

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10.1111/J.1469-7793.2000.T01-2-00349.X

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3

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522 Pt 3

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2000-02-01T00:00:00Z

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12601759

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10713961

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2269765

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