Characterization of recombinant human P2X4 receptor reveals pharmacological differences to the rat homologue
about
P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels.Molecular and functional properties of P2X receptors--recent progress and persisting challengesMechanism of ivermectin facilitation of human P2X4 receptor channelsProtein kinase C regulation of P2X3 receptors is unlikely to involve direct receptor phosphorylationZinc as Allosteric Ion Channel Modulator: Ionotropic Receptors as MetalloproteinsInsights into the channel gating of P2X receptors from structures, dynamics and small moleculesP2X4 receptors (P2X4Rs) represent a novel target for the development of drugs to prevent and/or treat alcohol use disordersPrinciples and properties of ion flow in P2X receptorsMolecular mechanism of ATP binding and ion channel activation in P2X receptorsMultiple P2X receptors on guinea-pig pelvic ganglion neurons exhibit novel pharmacological propertiesDevelopmental changes in P2X purinoceptors on glycinergic presynaptic nerve terminals projecting to rat substantia gelatinosa neuronesConductance of P2X4 purinergic receptor is determined by conformational equilibrium in the transmembrane regionPurinergic receptors activating rapid intracellular Ca increases in microglia.Damage-induced cell-cell communication in different cochlear cell types via two distinct ATP-dependent Ca wavesCardiac purinergic signalling in health and diseaseCloning and pharmacological characterization of the guinea pig P2X7 receptor orthologueP2X4 Receptor Function in the Nervous System and Current Breakthroughs in Pharmacology.Non-synonymous single nucleotide polymorphisms in the P2X receptor genes: association with diseases, impact on receptor functions and potential use as diagnosis biomarkersA fluorescence-detection size-exclusion chromatography-based thermostability assay for membrane protein precrystallization screeningCardiac P2X purinergic receptors as a new pathway for increasing Na⁺ entry in cardiac myocytes.Modulation of ATP-responses at recombinant rP2X4 receptors by extracellular pH and zincInhibition by ethanol of rat P2X(4) receptors expressed in Xenopus oocytesEvidence for P2Y1, P2Y2, P2Y6 and atypical UTP-sensitive receptors coupled to rises in intracellular calcium in mouse cultured superior cervical ganglion neurons and gliaAgonists and antagonists for P2 receptors.Activation and regulation of purinergic P2X receptor channelsStructure-based identification and characterisation of structurally novel human P2X7 receptor antagonistsP2 receptor subtypes in the cardiovascular system.Ligand-gated purinergic receptors regulate HIV-1 Tat and morphine related neurotoxicity in primary mouse striatal neuron-glia co-cultures.Structural insights into the nucleotide base specificity of P2X receptors.Structural interpretation of P2X receptor mutagenesis studies on drug actionA new role for P2X4 receptors as modulators of lung surfactant secretion.Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gatingModeling Interactions among Individual P2 Receptors to Explain Complex Response Patterns over a Wide Range of ATP Concentrations.Carbon monoxide is a rapid modulator of recombinant and native P2X(2) ligand-gated ion channels.P2X receptor subtype-specific modulation of excitatory and inhibitory synaptic inputs in the rat brainstem.Impaired P2X1 Receptor-Mediated Adhesion in Eosinophils from Asthmatic Patients.Molecular basis of selective antagonism of the P2X1 receptor for ATP by NF449 and suramin: contribution of basic amino acids in the cysteine-rich loop.Functional characterization of the P2X(4) receptor orthologuesMembrane topology of an ATP-gated ion channel (P2X receptor).Use of chimeras, point mutants, and molecular modeling to map the antagonist-binding site of 4,4',4″,4‴-(carbonylbis-(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakisbenzene-1,3-disulfonic acid (NF449) at P2X1 receptors for ATP.
P2860
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P2860
Characterization of recombinant human P2X4 receptor reveals pharmacological differences to the rat homologue
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Characterization of recombinan ...... fferences to the rat homologue
@ast
Characterization of recombinan ...... fferences to the rat homologue
@en
Characterization of recombinan ...... fferences to the rat homologue
@en-gb
Characterization of recombinan ...... fferences to the rat homologue
@nl
type
label
Characterization of recombinan ...... fferences to the rat homologue
@ast
Characterization of recombinan ...... fferences to the rat homologue
@en
Characterization of recombinan ...... fferences to the rat homologue
@en-gb
Characterization of recombinan ...... fferences to the rat homologue
@nl
prefLabel
Characterization of recombinan ...... fferences to the rat homologue
@ast
Characterization of recombinan ...... fferences to the rat homologue
@en
Characterization of recombinan ...... fferences to the rat homologue
@en-gb
Characterization of recombinan ...... fferences to the rat homologue
@nl
P2093
P921
P3181
P356
P1476
Characterization of recombinan ...... fferences to the rat homologue
@en
P2093
J M Gomez-Hernandez
M Garcia-Guzman
P304
P3181
P356
10.1124/MOL.51.1.109
P407
P577
1997-01-01T00:00:00Z