Recent Progress in the Structure Determination of GPCRs, a Membrane Protein Family with High Potential as Pharmaceutical Targets.

Sub-picomolar relaxin signalling by a pre-assembled RXFP1, AKAP79, AC2, beta-arrestin 2, PDE4D3 complex.

An N-terminal polybasic motif of G{alpha}q is required for signaling and influences membrane nanodomain distribution.

Exploring the binding-site crevice of a family B GPCR, the type 1 corticotropin releasing factor receptor.

Thinking outside of the (RGS) box: New Approaches to Therapeutic Targeting of Regulators of G protein Signaling.

Use of the GTPgammaS ([(35)S]GTPgammaS and Eu-GTPgammaS) binding assay for analysis of ligand potency and efficacy at G protein-coupled receptors.

Exploring the structure of opioid receptors with homology modeling based on single and multiple templates and subsequent docking: A comparative study.

Systematic Analysis of G Protein-Coupled Receptor Gene Expression in Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia Identifies Novel Targets for Pharmacological Control of Adrenal Cushing's Syndrome.

Transactivation of PDGFR-beta by dopamine D4 receptor does not require PDGFR dimerization.

Identification of a novel snake peptide toxin displaying high affinity and antagonist behaviour for the alpha(2)-adrenoceptors.

Formation of a ternary complex between NHERF1, {beta}-arrestin, and parathyroid hormone receptor.

Role of GABA(B) Receptors in Autonomic Control of Systemic Blood Pressure.

GABA(B) Receptors Physiological Functions and Mechanisms of Diversity.

Functional Modulation of GABA(B) Receptors by Protein Kinases and Receptor Trafficking.

Heterodimerization of the GABA(B) Receptor-Implications for GPCR Signaling and Drug Discovery.

Regulation of GPCR signal networks via membrane trafficking.

Melanocortin receptors and their accessory proteins.

Fluorescent protein complementation assays: new tools to study G protein-coupled receptor oligomerization and GPCR-mediated signaling.

Arresting a TRP channel [beta]-arrestin 1 mediates ubiquitination and functional downregulation of TRPV4.

N-Acyl amino acids and N-acyl neurotransmitter conjugates: neuromodulators and probes for new drug targets.