Homobivalent Dopamine D2 Receptor Ligands Modulate the Dynamic Equilibrium of D2 Monomers and Homo- and Heterodimers
Por um escritor misterioso
Last updated 01 março 2025
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A, the B max of [ 3 H]spiperone is unaffected by raclopride in the
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Receptor density influences ligand-induced dopamine D2L receptor homodimerization - ScienceDirect
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Design and Characterization of Superpotent Bivalent Ligands Targeting Oxytocin Receptor Dimers via a Channel-Like Structure
Optical Control of Dopamine D2-like Receptors with Cell-Specific Fast-Relaxing Photoswitches
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The dopamine D2 receptor dimer and its interaction with homobivalent antagonists: homology modeling, docking and molecular dynamics
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IJMS, Free Full-Text
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Schematic representation of wild type dopamine D 2 and D 3 receptors
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Comparison of simulated and actual raclopride saturation analysis of a
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NTS1R-D2R bivalent ligand induced calcium release in HT22 cells. (a)
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Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
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Frontiers Modulating brain integrative actions as a new perspective on pharmacological approaches to neuropsychiatric diseases
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Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
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Functional consequences of GPCR heterodimerization. (A). As in the case
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