Homobivalent Dopamine D2 Receptor Ligands Modulate the Dynamic Equilibrium of D2 Monomers and Homo- and Heterodimers

A, the B max of [ 3 H]spiperone is unaffected by raclopride in the

Receptor density influences ligand-induced dopamine D2L receptor homodimerization - ScienceDirect

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

The dopamine D2 receptor dimer and its interaction with homobivalent antagonists: homology modeling, docking and molecular dynamics

IJMS, Free Full-Text

Schematic representation of wild type dopamine D 2 and D 3 receptors

Comparison of simulated and actual raclopride saturation analysis of a

NTS1R-D2R bivalent ligand induced calcium release in HT22 cells. (a)

Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer

Frontiers Modulating brain integrative actions as a new perspective on pharmacological approaches to neuropsychiatric diseases

Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer

Functional consequences of GPCR heterodimerization. (A). As in the case