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Screening for GPCR Ligands Using Surface Plasmon Resonance
Iva Hopkins Navratilova (Lead / Corresponding author)
, Jeremy Besnard
, Andrew L. Hopkins
Research output
:
Contribution to journal
›
Article
›
peer-review
90
Citations (Scopus)
Overview
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Dive into the research topics of 'Screening for GPCR Ligands Using Surface Plasmon Resonance'. Together they form a unique fingerprint.
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Keyphrases
G Protein-coupled Receptor
100%
Ligand-receptor Binding
100%
Surface Plasmon Resonance
100%
Receptor-ligand Interaction
33%
Screening Method
33%
Allosteric Ligands
33%
Signaling Pathway
16%
Functional Response
16%
Binding Site
16%
Novel Ligands
16%
High-throughput
16%
Ligand Binding
16%
Drug Target
16%
Drug Class
16%
Label-free
16%
Assay Method
16%
Primary Screening
16%
Biosensor Assay
16%
Cell-free
16%
Site Probes
16%
Direct Screening
16%
C-C Chemokine Receptor Type 5 (CCR5)
16%
Orthogonal Screening
16%
Displacement Assay
16%
Assay Formats
16%
Allosteric Modulation
16%
Receptor Binding Assay
16%
Indirect Assay
16%
Label-free Screening
16%
Ligand Displacement
16%
Chemokine Receptor
16%
Probe Dependence
16%
Free-free
16%
Functional Selectivity
16%
Assay Protocol
16%
Chemistry
Binding Site
100%
Drug Target
100%
Surface Plasmon Resonance
100%
Ligand Binding
100%
Chemokine
100%
Biochemistry, Genetics and Molecular Biology
G Protein Coupled Receptor
100%
Surface Plasmon Resonance
100%
Binding Site
16%
Allosteric Regulation
16%
Ligand Binding
16%
Chemokine Receptor
16%
CCR5
16%
Pharmacology, Toxicology and Pharmaceutical Science
G Protein Coupled Receptor
100%
Surface Plasmon Resonance
100%
Binding Site
16%
Receptor
16%
Chemokine Receptor CCR5
16%
Functional Selectivity
16%