Mechanisms of cross-talk between G-protein-coupled receptors resulting in enhanced release of intracellular Ca2+. - Wikidata - awgldk - TriplyDB

Mechanisms of cross-talk between G-protein-coupled receptors resulting in enhanced release of intracellular Ca2+.

Mechanisms of cross-talk between G-protein-coupled receptors resulting in enhanced release of intracellular Ca2+.

http://www.wikidata.org/entity/Q35147150

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Phosphorylation of GRK1 and GRK7 by cAMP-dependent protein kinase attenuates their enzymatic activities CXCL5 mediates UVB irradiation-induced pain Selective coupling of type 6 adenylyl cyclase with type 2 IP3 receptors mediates direct sensitization of IP3 receptors by cAMP A comprehensive pathway map of epidermal growth factor receptor signaling Inhibitory Effect of Serotonin Antagonist on Leukocyte-Endothelial Interactions In Vivo and In Vitro A dual receptor crosstalk model of G-protein-coupled signal transduction Regulation of inositol 1,4,5-trisphosphate receptors by cAMP independent of cAMP-dependent protein kinase Signaling and cross-talk by C5a and UDP in macrophages selectively use PLCbeta3 to regulate intracellular free calcium.Synergistic Ca2+ responses by G{alpha}i- and G{alpha}q-coupled G-protein-coupled receptors require a single PLC{beta} isoform that is sensitive to both G{beta}{gamma} and G{alpha}q.Agonist-dependent mu-opioid receptor signaling can lead to heterologous desensitization.Synergistic activation of phospholipase C-beta3 by Galpha(q) and Gbetagamma describes a simple two-state coincidence detector Activation of a TRP-like channel and intracellular Ca2+ dynamics during phospholipase-C-mediated cell death.Role of CD38, a cyclic ADP-ribosylcyclase, in morphine antinociception and tolerance.Norepinephrine: a neuromodulator that boosts the function of multiple cell types to optimize CNS performance Subthreshold α₂-adrenergic activation counteracts glucagon-like peptide-1 potentiation of glucose-stimulated insulin secretion.Full-length and truncated neurokinin-1 receptor expression and function during monocyte/macrophage differentiation.Interaction of actin with carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) receptor in liposomes is Ca2+- and phospholipid-dependent.Kisspeptin induction of somatolactin-α release in goldfish pituitary cells: functional role of cAMP/PKA-, PLC/PKC-, and Ca(2+)/calmodulin-dependent cascades.Infection by Toxoplasma gondii, a severe parasite in neonates and AIDS patients, causes impaired anion secretion in airway epithelia.Association of corticotropin-releasing hormone receptor-2 genetic variants with acute bronchodilator response in asthma.Hierarchical feedback modules and reaction hubs in cell signaling networks.Gi-coupled γ-aminobutyric acid-B receptors cross-regulate phospholipase C and calcium in airway smooth muscle.Molecular Insights into the Transmembrane Domain of the Thyrotropin Receptor Identification of an alternative G{alpha}q-dependent chemokine receptor signal transduction pathway in dendritic cells and granulocytes.Host gene-encoded severe lung TB: from genes to the potential pathways Substance P (SP) enhances CCL5-induced chemotaxis and intracellular signaling in human monocytes, which express the truncated neurokinin-1 receptor (NK1R)Cross-talk between signaling pathways can generate robust oscillations in calcium and cAMP.Mitochondrial reactive oxygen species mediate GPCR-induced TACE/ADAM17-dependent transforming growth factor-alpha shedding.Ca2+ signaling in airway epithelial cells facilitates leukocyte recruitment and transepithelial migration.The orexin 1 receptor modulates kappa opioid receptor function via a JNK-dependent mechanism.Adenosine A1 and A2A Receptors in the Brain: Current Research and Their Role in Neurodegeneration.Effect of 2,5-dimethylphenol on Ca(2+) movement and viability in PC3 human prostate cancer cells.A role for inflammatory mediators in heterologous desensitization of CysLT1 receptor in human monocytes.Full and partial agonists of muscarinic M3 receptors reveal single and oscillatory Ca2+ responses by beta 2-adrenoceptors A crucial role for cAMP and protein kinase A in D1 dopamine receptor regulated intracellular calcium transients.Agonist-dependent cannabinoid receptor signalling in human trabecular meshwork cells.Modulation of Gq-protein-coupled inositol trisphosphate and Ca2+ signaling by the membrane potential.Transcriptional activation of the human Galphai2 gene promoter through nuclear factor-kappaB and antioxidant response elements.Co-incident signalling between mu-opioid and M3 muscarinic receptors at the level of Ca2+ release from intracellular stores: lack of evidence for Ins(1,4,5)P3 receptor sensitization.Lysophosphatidylcholine and 7-oxocholesterol modulate Ca2+ signals and inhibit the phosphorylation of endothelial NO synthase and cytosolic phospholipase A2.

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Mechanisms of cross-talk between G-protein-coupled receptors resulting in enhanced release of intracellular Ca2+.

http://www.wikidata.org/entity/Q35147150

description

2003 nî lūn-bûn

@nan

2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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type

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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Biochemical Journal

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Mechanisms of cross-talk betwe ...... release of intracellular Ca2+.

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P2093

Gary B Willars

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

Graeme F Wilkinson

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Tim D Werry

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

P2860

Heterodimerization is required for the formation of a functional GABA(B) receptor

Ca2+/Calmodulin reverses phosphatidylinositol 3,4, 5-trisphosphate-dependent inhibition of regulators of G protein-signaling GTPase-activating protein activity

AT1-receptor heterodimers show enhanced G-protein activation and altered receptor sequestration

Ca(2+) signalling by recombinant human CXCR2 chemokine receptors is potentiated by P2Y nucleotide receptors in HEK cells

The human thyrotropin receptor: a heptahelical receptor capable of stimulating members of all four G protein families

Phospholipase C-beta 1 is a GTPase-activating protein for Gq/11, its physiologic regulator

Differential regulation of nicotinic acid-adenine dinucleotide phosphate and cADP-ribose production by cAMP and cGMP

G-protein-coupled receptor heterodimerization modulates receptor function

Heteromeric association creates a P2Y-like adenosine receptor

Pharmacological properties of the Ca2+-release mechanism sensitive to NAADP in the sea urchin egg

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281-296

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scholarly article

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10.1042/BJ20030312

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P433

Pt 2

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P478

374

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2003-09-01T00:00:00Z

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7073778

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12790797

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G protein-coupled receptor

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1223610

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