A fluorescent ligand-binding alternative using Tag-lite® technology.
about
Large-scale production and protein engineering of G protein-coupled receptors for structural studiesFluorescent approaches for understanding interactions of ligands with G protein coupled receptorsGlucagon-Like Peptide-1 and Its Class B G Protein-Coupled Receptors: A Long March to Therapeutic SuccessesIdentification of anti-malarial compounds as novel antagonists to chemokine receptor CXCR4 in pancreatic cancer cellsA Comparative Study of Impedance versus Optical Label-Free Systems Relative to Labelled Assays in a Predominantly Gi Coupled GPCR (C5aR) Signalling.Fragment screening at adenosine-A(3) receptors in living cells using a fluorescence-based binding assay.A computationally designed water-soluble variant of a G-protein-coupled receptor: the human mu opioid receptor.Bridged cyclams as imaging agents for chemokine receptor 4 (CXCR4)Portraying G protein-coupled receptors with fluorescent ligandsCharacterization of a computationally designed water-soluble human μ-opioid receptor variant using available structural informationOxytocin and vasopressin agonists and antagonists as research tools and potential therapeutics.BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues.Establishment of a novel cell-based assay for screening small molecule antagonists of human interleukin-6 receptor.Application of BRET to monitor ligand binding to GPCRs.Target engagement and drug residence time can be observed in living cells with BRET.Vasopressin inhibits LTP in the CA2 mouse hippocampal area.Untangling dopamine-adenosine receptor-receptor assembly in experimental parkinsonism in ratsHIV cell fusion assay: phenotypic screening tool for the identification of HIV entry inhibitors via CXCR4.GPCR ligand dendrimer (GLiDe) conjugates: adenosine receptor interactions of a series of multivalent xanthine antagonistsDisclosing the CXCR4 expression in lymphoproliferative diseases by targeted molecular imagingFluorescence- and bioluminescence-based approaches to study GPCR ligand binding.Natural amines inhibit activation of human plasmacytoid dendritic cells through CXCR4 engagement.Monitoring Gq-coupled receptor response through inositol phosphate quantification with the IP-One assay.An update of novel screening methods for GPCR in drug discovery.Measurement of G protein-coupled receptor surface expression.Evolution of biologics screening technologies.EuroTracker® dyes: design, synthesis, structure and photophysical properties of very bright europium complexes and their use in bioassays and cellular optical imaging.Rational design of CXCR4 specific antibodies with elongated CDRs.RgIA4 Potently Blocks Mouse α9α10 nAChRs and Provides Long Lasting Protection against Oxaliplatin-Induced Cold Allodynia.A Broad G Protein-Coupled Receptor Internalization Assay that Combines SNAP-Tag Labeling, Diffusion-Enhanced Resonance Energy Transfer, and a Highly Emissive Terbium Cryptate.Drug discovery opportunities and challenges at g protein coupled receptors for long chain free Fatty acids.A homogeneous single-label quenching resonance energy transfer assay for a δ-opioid receptor-ligand using intact cells.Fluorescent ligands for G protein-coupled receptors: illuminating receptor-ligand interactions for drug discovery.Original Fluorescent Ligand-Based Assays Open New Perspectives in G-Protein Coupled Receptor Drug Screening.Time-resolved fluorescence ligand binding for G protein-coupled receptors.Versatility of homogeneous time-resolved fluorescence resonance energy transfer assays for biologics drug discovery.Creating infinite contrast in fluorescence microscopy by using lanthanide centered emission.A Time-Resolved FRET Cell-Based Binding Assay for the Apelin Receptor.Multifaceted C-X-C Chemokine Receptor 4 (CXCR4) Inhibition Interferes with Anti-Vascular Endothelial Growth Factor Therapy-Induced Glioma Dissemination.Convenient Access to Fluorescent Probes by Chemoselective Acylation of Hydrazinopeptides: Application to the Synthesis of the First Far-Red Ligand for Apelin Receptor Imaging.
P2860
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P2860
A fluorescent ligand-binding alternative using Tag-lite® technology.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
A fluorescent ligand-binding alternative using Tag-lite® technology.
@en
A fluorescent ligand-binding alternative using Tag-lite® technology.
@nl
type
label
A fluorescent ligand-binding alternative using Tag-lite® technology.
@en
A fluorescent ligand-binding alternative using Tag-lite® technology.
@nl
prefLabel
A fluorescent ligand-binding alternative using Tag-lite® technology.
@en
A fluorescent ligand-binding alternative using Tag-lite® technology.
@nl
P2093
P356
P1476
A fluorescent ligand-binding alternative using Tag-lite® technology.
@en
P2093
Chloe Boisseau
Emmanuel Bourrier
Eric Trinquet
Fabienne Charrier-Savournin
Jurriaan M Zwier
Ludovic Nicolas
Martin Cottet
Michel Fink
Nadia Oueslati
Nathalie Gregor
P304
P356
10.1177/1087057110384611
P577
2010-10-25T00:00:00Z