Homo- and hetero-oligomeric interactions between G-protein-coupled receptors in living cells monitored by two variants of bioluminescence resonance energy transfer (BRET): hetero-oligomers between receptor subtypes form more efficiently than between
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Cys-27 variant of human δ-opioid receptor modulates maturation and cell surface delivery of Phe-27 variant via heteromerizationReceptor heteromerization and drug discovery.Allostery at G protein-coupled receptor homo- and heteromers: uncharted pharmacological landscapesAntibodies to probe endogenous G protein-coupled receptor heteromer expression, regulation, and functionMechanism and function of Drosophila capa GPCR: a desiccation stress-responsive receptor with functional homology to human neuromedinU receptorOligomerization of the yeast alpha-factor receptor: implications for dominant negative effects of mutant receptors.Homo- and hetero-oligomerization of thyrotropin-releasing hormone (TRH) receptor subtypes. Differential regulation of beta-arrestins 1 and 2Functional characterization of G-protein-coupled receptors: a bioinformatics approach.Physical and functional interaction between CB1 cannabinoid receptors and beta2-adrenoceptorsThe Epstein-Barr virus-encoded G protein-coupled receptor BILF1 hetero-oligomerizes with human CXCR4, scavenges Gαi proteins, and constitutively impairs CXCR4 functioning.Type 1 cannabinoid receptor ligands display functional selectivity in a cell culture model of striatal medium spiny projection neurons.Making structural sense of dimerization interfaces of delta opioid receptor homodimers.Design strategies for bivalent ligands targeting GPCRs.Oligomerisation of C. elegans olfactory receptors, ODR-10 and STR-112, in yeast.Monitoring the formation of dynamic G-protein-coupled receptor-protein complexes in living cells.Revolution in GPCR signalling: opioid receptor heteromers as novel therapeutic targets: IUPHAR review 10.Rhodopsin self-associates in asolectin liposomes.Enabling systematic interrogation of protein-protein interactions in live cells with a versatile ultra-high-throughput biosensor platform.In vivo opioid receptor heteromerization: where do we stand?Targeting the cis-dimerization of LINGO-1 with low MW compounds affects its downstream signallingRole of membrane integrity on G protein-coupled receptors: Rhodopsin stability and function.Demonstration of a direct interaction between β2-adrenergic receptor and insulin receptor by BRET and bioinformatics.Roles of G-protein-coupled receptor dimerization.High Efficacy but Low Potency of δ-Opioid Receptor-G Protein Coupling in Brij-58-Treated, Low-Density Plasma Membrane Fragments.Regulation of cell migration by sphingomyelin synthases: sphingomyelin in lipid rafts decreases responsiveness to signaling by the CXCL12/CXCR4 pathway.G-protein-coupled receptors in drug discovery: nanosizing using cell-free technologies and molecular biology approaches.Proximal, selective, and dynamic interactions between integrin alphaIIbbeta3 and protein tyrosine kinases in living cells.Application of bioluminescence resonance energy transfer (BRET) for biomolecular interaction studies.Molecular Pharmacology of δ-Opioid Receptors.Biosensing and imaging based on bioluminescence resonance energy transfer.Disease-specific heteromerization of G-protein-coupled receptors that target drugs of abuseG-protein-coupled receptor type A heteromers as an emerging therapeutic target.Rational design of novel red-shifted BRET pairs: Platforms for real-time single-chain protease biosensors.The Conserved Arginine Cluster in the Insert of the Third Cytoplasmic Loop of the Long Form of the D₂ Dopamine Receptor (D2L-R) Acts as an Intracellular Retention Signal.A cell-based protein-protein interaction method using a permuted luciferase reporter.Improved donor/acceptor BRET couples for monitoring beta-arrestin recruitment to G protein-coupled receptors.CXCR2 chemokine receptor antagonism enhances DOP opioid receptor function via allosteric regulation of the CXCR2-DOP receptor heterodimer.Direct assessment of CXCR4 mutant conformations reveals complex link between receptor structure and G(alpha)(i) activation.Probing intermolecular protein-protein interactions in the calcium-sensing receptor homodimer using bioluminescence resonance energy transfer (BRET).Receptor Quaternary Organization Explains G Protein-Coupled Receptor Family Structure.
P2860
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P2860
Homo- and hetero-oligomeric interactions between G-protein-coupled receptors in living cells monitored by two variants of bioluminescence resonance energy transfer (BRET): hetero-oligomers between receptor subtypes form more efficiently than between
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
Homo- and hetero-oligomeric in ...... more efficiently than between
@en
type
label
Homo- and hetero-oligomeric in ...... more efficiently than between
@en
prefLabel
Homo- and hetero-oligomeric in ...... more efficiently than between
@en
P2093
P2860
P356
P1433
P1476
Homo- and hetero-oligomeric in ...... more efficiently than between
@en
P2093
Douglas Ramsay
Elaine Kellett
Graeme Milligan
Mary McVey
Stephen Rees
P2860
P304
P356
10.1042/BJ20020251
P407
P577
2002-07-01T00:00:00Z