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British Journal of Pharmacology|April 23, 2014
Effect of a toggle switch mutation in TM6 of the human adenosine A₃ receptor on Gi protein-dependent signalling and Gi-independent receptor internalizationLeigh A Stoddart, Barrie Kellam, Stephen J Briddon, et al.
Neuropharmacology|May 17, 2015
Probing the pharmacology of G protein-coupled receptors with fluorescent ligandsLeigh A Stoddart, Laura E Kilpatrick, Stephen J Briddon, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 25, 2019
Application of Fluorescent Purinoceptor Antagonists for Bioluminescence Resonance Energy Transfer Assays and Fluorescent MicroscopyMark Soave, Joëlle Goulding, Robert Markus, et al.
Pharmacology Research & Perspectives|September 3, 2016
Use of a new proximity assay (NanoBRET) to investigate the ligand-binding characteristics of three fluorescent ligands to the human <i>β</i><sub>1</sub>-adrenoceptor expressed in HEK-293 cellsMark Soave, Leigh A Stoddart, Alastair Brown, et al.
Molecular and Cellular Endocrinology|February 11, 2019
Binding kinetics of ligands acting at GPCRsDavid A Sykes, Leigh A Stoddart, Laura E Kilpatrick, et al.
The Journal of Biological Chemistry|April 29, 2009
The action and mode of binding of thiazolidinedione ligands at free fatty acid receptor 1Nicola J Smith, Leigh A Stoddart, Nicola M Devine, et al.
The Journal of Biological Chemistry|September 20, 2008
Conserved polar residues in transmembrane domains V, VI, and VII of free fatty acid receptor 2 and free fatty acid receptor 3 are required for the binding and function of short chain fatty acidsLeigh A Stoddart, Nicola J Smith, Laura Jenkins, et al.
Neuropharmacology|May 5, 2015
Direct visualisation of internalization of the adenosine A3 receptor and localization with arrestin3 using a fluorescent agonistLeigh A Stoddart, Andrea J Vernall, Stephen J Briddon, et al.
The Journal of Biological Chemistry|February 1, 2012
Functional homomers and heteromers of dopamine D2L and D3 receptors co-exist at the cell surfaceChantevy Pou, Clotilde Mannoury la Cour, Leigh A Stoddart, et al.
Journal of Medicinal Chemistry|January 27, 2012
Highly potent and selective fluorescent antagonists of the human adenosine A₃ receptor based on the 1,2,4-triazolo[4,3-a]quinoxalin-1-one scaffoldAndrea J Vernall, Leigh A Stoddart, Stephen J Briddon, et al.
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