Engineered G protein-coupled receptors (GPCRs) are commonly used in chemogenetics as designer receptors Although several GPCRs have been studied in astrocytes using a chemogenetic approach, the functional

target for control of the fall webworm Hyphantria cunea Background: Insect G protein-coupled receptors (GPCRs HLGR2 is a typical GPCR and shows high structural and sequence similarity with other insect LGR2 proteins

The D1 receptor (D1R) is a Gαs/olf-coupled GPCR which activates a cAMP/PKA/DARPP-32 signalling cascade Finally, we report that JQ1 treatment downregulated expression of many GPCRs and also impaired ERK1/2

This study demonstrated Gαq-G-protein coupled receptor (GPCR)-mediated [Ca2+]i signaling involvement cartilage-like matrix production, and it established hM3Dq as a powerful tool for elucidating the role of GPCR-mediated

Nanobody binding stabilizes G-protein-coupled receptors (GPCR) in a fully active state and modulates Altogether, our results provide insights into the effect of intracellular binding partners on the GPCR

However, many new targets, such as Mas-related GPCRs and unexpected new pathways need to be also explored

These disorders are mainly related to the abnormalities in the rod G protein-coupled receptor (GPCR),

residues spans from the extracellular surface to the transmembrane area, linking with canonical class A GPCR activation motifs to initiate proton-sensing GPCRs.

Many G-protein-coupled receptors (GPCRs) including EP4 are localized in cilia for modulating cAMP signaling

Further difficulties arise from the existence of cross-reactivity with other GPCRs and differences in of chemokine receptors which are regulated by globular protein ligands, unlike most of the class A GPCRs

cryo-EM has enabled insights into important drug target families such as G protein-coupled receptors (GPCRs

Given that postsynaptic latrophilin adhesion-GPCRs drive synapse formation and produce cAMP, we suggest

G protein-coupled receptors (GPCRs) transmit extracellular signals to the inside by activation of intracellular

characterize ligand interactions with cell surface membrane proteins such as G-protein coupled receptors (GPCRs

"The effects of the neurohormone melatonin are mediated by the activation of the GPCRs MT1 and MT2 in

and review Odorant receptors (ORs) account for about 60% of all human G protein-coupled receptors (GPCRs

their functional activities are achieved by binding to the cell surface G protein-coupled receptors (GPCRs

is a key protein that mediates desensitization and internalization of G protein-coupled receptors (GPCRs

Colocalization of different actions of GPCRs provide synaptic integration within presynaptic terminals

dependent kinase inhibitor 1B; CQ: chloroquine; E2F1: E2F transcription factor 1; FBS: fetal bovine serum; GPCRs

Exendin-4, and possibly through G protein-coupled receptors (GPCRs), increases levels of cAMP and upregulates

Opioid receptors belong to class A of G protein-coupled receptors or GPCRs and signaled mainly through