about
Presynaptic control of striatal glutamatergic neurotransmission by adenosine A1-A2A receptor heteromersUbiquitination of CXCR7 controls receptor traffickingNovel GPCR paradigms at the μ-opioid receptorRegulation of G protein-coupled receptors by allosteric ligandsBiological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivityStructural basis of receptor sulfotyrosine recognition by a CC chemokine: the N-terminal region of CCR3 bound to CCL11/eotaxin-1Coaggregation, cointernalization, and codesensitization of adenosine A2A receptors and dopamine D2 receptorsAdenosine A2A and dopamine D2 heteromeric receptor complexes and their functionAdenosine A2A receptor and dopamine D3 receptor interactions: evidence of functional A2A/D3 heteromeric complexesMolecular mechanisms involved in the adenosine A and A receptor-induced neuronal differentiation in neuroblastoma cells and striatal primary culturesDiscovery, synthesis, and molecular pharmacology of selective positive allosteric modulators of the δ-opioid receptor.Endothelin-converting enzyme 1 and β-arrestins exert spatiotemporal control of substance P-induced inflammatory signals.Allosteric modulation of M1 muscarinic acetylcholine receptor internalization and subcellular trafficking.Chemical subtleties in small-molecule modulation of peptide receptor function: the case of CXCR3 biaryl-type ligands.Mechanistic insights into allosteric structure-function relationships at the M1 muscarinic acetylcholine receptor.Structure-based ligand discovery targeting orthosteric and allosteric pockets of dopamine receptors.A Monod-Wyman-Changeux mechanism can explain G protein-coupled receptor (GPCR) allosteric modulationAdenosine A2A-dopamine D2 receptor-receptor heteromers. Targets for neuro-psychiatric disorders.Design and receptor interactions of obligate dimeric mutant of chemokine monocyte chemoattractant protein-1 (MCP-1).Protein Kinase D and Gβγ Subunits Mediate Agonist-evoked Translocation of Protease-activated Receptor-2 from the Golgi Apparatus to the Plasma Membrane.Distribution and trafficking of the μ-opioid receptor in enteric neurons of the guinea pig.The role of kinetic context in apparent biased agonism at GPCRs.Intramembrane receptor-receptor interactions: a novel principle in molecular medicine.Tyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1)The bile acid receptor TGR5 does not interact with β-arrestins or traffic to endosomes but transmits sustained signals from plasma membrane rafts.Proposed Mode of Binding and Action of Positive Allosteric Modulators at Opioid Receptors.Agonist-biased trafficking of somatostatin receptor 2A in enteric neuronsMolecular determinants of allosteric modulation at the M1 muscarinic acetylcholine receptor.Pharmacological modulation of chemokine receptor function.Allostery in GPCRs: 'MWC' revisited.Ticks from diverse genera encode chemokine-inhibitory evasin proteins.Detection and quantification of allosteric modulation of endogenous m4 muscarinic acetylcholine receptor using impedance-based label-free technology in a neuronal cell line.Synthesis, Biological Evaluation, and Utility of Fluorescent Ligands Targeting the μ-Opioid Receptor.Neurokinin 1 receptor signaling in endosomes mediates sustained nociception and is a viable therapeutic target for prolonged pain relief.Synthesis, modeling and functional activity of substituted styrene-amides as small-molecule CXCR7 agonists.Plasma membrane localization of the μ-opioid receptor controls spatiotemporal signaling.Key determinants of selective binding and activation by the monocyte chemoattractant proteins at the chemokine receptor CCR2.Combining mass spectrometry and pull-down techniques for the study of receptor heteromerization. Direct epitope-epitope electrostatic interactions between adenosine A2A and dopamine D2 receptors.Homodimerization of adenosine A2A receptors: qualitative and quantitative assessment by fluorescence and bioluminescence energy transfer.Constitutive activity of the cannabinoid CB1 receptor regulates the function of co-expressed Mu opioid receptors.
P50
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P50
description
hulumtuese
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onderzoeker
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հետազոտող
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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M Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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Meritxell Canals
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P106
P1153
7006381076
P21
P31
P496
0000-0002-7942-5006