Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels - Wikidata - thesis-toulmin - TriplyDB

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

http://www.wikidata.org/entity/Q35089887

about

Modulation of K2P 2.1 and K2P 10.1 K(+) channel sensitivity to carvedilol by alternative mRNA translation initiation.TASK1 (K(2P)3.1) K(+) channel inhibition by endothelin-1 is mediated through Rho kinase-dependent phosphorylation PKC-dependent activation of human K(2P) 18.1 K(+) channels.Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore.Mechanisms of zolpidem-induced long QT syndrome: acute inhibition of recombinant hERG K(+) channels and action potential prolongation in human cardiomyocytes derived from induced pluripotent stem cells Cardiac potassium channel subtypes: new roles in repolarization and arrhythmia.The role of acid-sensitive two-pore domain potassium channels in cardiac electrophysiology: focus on arrhythmias.Novel ion channel targets in atrial fibrillation.Functional characterization of zebrafish K2P18.1 (TRESK) two-pore-domain K+ channels.Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels.

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Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

http://www.wikidata.org/entity/Q35089887

description

2011 nî lūn-bûn

@nan

2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

@ast

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

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type

label

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

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Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

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prefLabel

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

@ast

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

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J.1476-5381.2011.01319.X

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British Journal of Pharmacology

P1476

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels

@en

P2093

A-K Rahm

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C Seyler

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D Thomas

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E Ficker

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H A Katus

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I Staudacher

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J Gierten

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J Kisselbach

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K Staudacher

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K Trappe

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P2860

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

Regulation of two-pore-domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein

Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3

Inhalational anesthetics activate two-pore-domain background K+ channels

Potassium leak channels and the KCNK family of two-P-domain subunits

Regulation of cardiac inwardly rectifying potassium current IK1 and Kir2.x channels by endothelin-1

Molecular background of leak K+ currents: two-pore domain potassium channels

International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels

The endocannabinoid anandamide is a direct and selective blocker of the background K(+) channel TASK-1.

An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum

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1099-1110

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scholarly article

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10.1111/J.1476-5381.2011.01319.X

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