An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum
about
p11, an annexin II subunit, an auxiliary protein associated with the background K+ channel, TASK-1A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids.An oxygen-, acid- and anaesthetic-sensitive TASK-like background potassium channel in rat arterial chemoreceptor cellsSelective block of the human 2-P domain potassium channel, TASK-3, and the native leak potassium current, IKSO, by zincKcnkø: single, cloned potassium leak channels are multi-ion poresThe endocannabinoid anandamide is a direct and selective blocker of the background K(+) channel TASK-1.Thyrotropin-releasing hormone increases GABA release in rat hippocampusConvergent and reciprocal modulation of a leak K+ current and I(h) by an inhalational anaesthetic and neurotransmitters in rat brainstem motoneurones.Rapid developmental maturation of neocortical FS cell intrinsic excitability.Multiple ionic mechanisms mediate inhibition of rat motoneurones by inhalation anaesthetics.SUMOylation silences heterodimeric TASK potassium channels containing K2P1 subunits in cerebellar granule neurons.Somato-dendritic mechanisms underlying the electrophysiological properties of hypothalamic magnocellular neuroendocrine cells: a multicompartmental model study.Distinct subclassification of DRG neurons innervating the distal colon and glans penis/distal urethra based on the electrophysiological current signature.Strain differences in pH-sensitive K+ channel-expressing cells in chemosensory and nonchemosensory brain stem nuclei.Carvedilol targets human K2P 3.1 (TASK1) K+ leak channelsThe Caenorhabditis elegans iodotyrosine deiodinase ortholog SUP-18 functions through a conserved channel SC-box to regulate the muscle two-pore domain potassium channel SUP-9.A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons.Substance P Depolarizes Lamprey Spinal Cord Neurons by Inhibiting Background Potassium Channels.Opening and closing of KCNKO potassium leak channels is tightly regulated.Neuronal two-pore-domain potassium channels and their regulation by G protein-coupled receptors.Ethanol inhibition of m-current and ethanol-induced direct excitation of ventral tegmental area dopamine neurons.The selectivity, voltage-dependence and acid sensitivity of the tandem pore potassium channel TASK-1: contributions of the pore domains.The Possible Role of TASK Channels in Rank-Ordered Recruitment of Motoneurons in the Dorsolateral Part of the Trigeminal Motor Nucleus.Is a new paradigm needed to explain how inhaled anesthetics produce immobility?cGMP does not activate two-pore domain K+ channels in cerebrovascular smooth muscle.TASK-1 (KCNK3) and TASK-3 (KCNK9) tandem pore potassium channel antagonists stimulate breathing in isoflurane-anesthetized rats.Gating of two pore domain potassium channels.Investigation of the role of TASK-2 channels in rat pulmonary arteries; pharmacological and functional studies following RNA interference procedures.Functional and molecular identification of a TASK-1 potassium channel regulating chloride secretion through CFTR channels in the shark rectal gland: implications for cystic fibrosis.TASK-1 channels in oligodendrocytes: a role in ischemia mediated disruptionThe response of the tandem pore potassium channel TASK-3 (K(2P)9.1) to voltage: gating at the cytoplasmic mouth.Increases in spinal cerebrospinal fluid potassium concentration do not increase isoflurane minimum alveolar concentration in ratsTASK channels contribute to the K+-dominated leak current regulating respiratory rhythm generation in vitro.Functional evidence of a role for two-pore domain potassium channels in rat mesenteric and pulmonary arteries.Local anaesthetics block hyperpolarization-activated inward current in rat small dorsal root ganglion neurones.Inhibition of a TREK-like K+ channel current by noradrenaline requires both β1- and β2-adrenoceptors in rat atrial myocytes.Grafting voltage and pharmacological sensitivity in potassium channelsA novel O2-sensing mechanism in rat glossopharyngeal neurones mediated by a halothane-inhibitable background K+ conductance.Presynaptic modulation of rat arterial chemoreceptor function by 5-HT: role of K+ channel inhibition via protein kinase C.GABA mediates autoreceptor feedback inhibition in the rat carotid body via presynaptic GABAB receptors and TASK-1.
P2860
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P2860
An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum
description
1998 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1998
@ast
im Februar 1998 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1998/02/01)
@sk
vědecký článek publikovaný v roce 1998
@cs
wetenschappelijk artikel (gepubliceerd op 1998/02/01)
@nl
наукова стаття, опублікована в лютому 1998
@uk
مقالة علمية (نشرت في فبراير 1998)
@ar
name
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@ast
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@en
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@nl
type
label
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@ast
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@en
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@nl
prefLabel
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@ast
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@en
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@nl
P2093
P3181
P1476
An open rectifier potassium ch ...... dem cloned from rat cerebellum
@en
P2093
B D Winegar
C H Kindler
D Leonoudakis
D M Taylor
J R Forsayeth
R A Chavez
P304
P3181
P356
10.1523/JNEUROSCI.18-03-00868.1998
P407
P577
1998-02-01T00:00:00Z