Cell-targeted PD-1 agonists that mimic PD-L1 are potent T cell inhibitors by Curnock, Adam P, Bossi, Giovanna, Kumaran, Jyothi, Bawden, Lindsay J, Figueiredo, Rita, Tawar, Rajeevkumar, Wiseman, Katherine, Henderson, Emma, Hoong, Sec Julie, Gonzalez, Veronica, Ghadbane, Hemza, Knight, David Eo, O'Dwyer, Ronan, Overton, David X, Lucato, Christina M, Smith, Nicola Mg, Reis, Carlos R, Page, Keith, Whaley, Lorraine M, McCully, Michelle L, Hearty, Stephen, Mahon, Tara M, Weber, Peter

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Design and Optimization of Selective Protein Kinase C θ (PKCθ) Inhibitors for the Treatment of Autoimmune Diseases by Jimenez, Juan-Miguel, Boyall, Dean, Brenchley, Guy, Collier, Philip N, Davis, Christopher J, Fraysse, Damien, Keily, Shazia B, Henderson, Jaclyn, Miller, Andrew, Pierard, Francoise, Settimo, Luca, Twin, Heather C, Bolton, Claire M, Curnock, Adam P, Chiu, Peter, Tanner, Adam J, Young, Stephen

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Discovery and Structure−Activity Relationship of 3-Aminopyrid-2-ones as Potent and Selective Interleukin-2 Inducible T-Cell Kinase (Itk) Inhibitors by Charrier, Jean-Damien, Miller, Andrew, Kay, David P, Brenchley, Guy, Twin, Heather C, Collier, Philip N, Ramaya, Sharn, Keily, Shazia B, Durrant, Steven J, Knegtel, Ronald M. A, Tanner, Adam J, Brown, Kieron, Curnock, Adam P, Jimenez, Juan-Miguel

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Chemokine signalling: pivoting around multiple phosphoinositide 3‐kinases by Curnock, Adam P., Logan, Marisa K., Ward, Stephen G.

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Optimal Chemotactic Responses of Leukemic T Cells to Stromal Cell-Derived Factor-1 Requires the Activation of Both Class IA and IB Phosphoinositide 3-Kinases by Curnock, Adam P, Sotsios, Yannis, Wright, Karen L, Ward, Stephen G

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Development and characterisation of tetracycline-regulated phosphoinositide 3-kinase mutants: assessing the role of multiple phosphoinositide 3-kinases in chemokine signaling by Curnock, Adam P., Ward, Stephen G.

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Dihydroorotate Dehydrogenase Is a High Affinity Binding Protein for A77 1726 and Mediator of a Range of Biological Effects of the Immunomodulatory Compound (∗) by Williamson, Richard A., Yea, Christopher M., Robson, Peter A., Curnock, Adam P., Gadher, Suresh, Hambleton, Anne B., Woodward, Katherine, Bruneau, Jean-Michel, Hambleton, Philip, Moss, David, Thomson, T. Andrew, Spinella-Jaegle, Sylvian, Morand, Philippe, Courtin, Olivier, Sautés, Catherine, Westwood, Robert, Hercend, Thierry, Kuo, Elizabeth A., Ruuth, Erik

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LY294002-Mediated Inhibition of Phosphatidylinositol 3-Kinase Activity Triggers Growth Inhibition and Apoptosis in CD40-Triggered Ramos–Burkitt Lymphoma B Cells by Curnock, Adam P., Knox, Kirstine A.

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Inhibition of stimulated Jurkat cell adenosine 3′,5′-cyclic monophosphate synthesis by the immunomodulatory compound HR325 by Curnock, Adam P., Thomson, T.Andrew, Westwood, Robert, Kuo, Elizabeth A., Williamson, Richard A., Yea, Christopher M., Ruuthb, Erik

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Potencies of Leflunomide and HR325 as Inhibitors of Prostaglandin Endoperoxide H Synthase-1 and -2: Comparison with Nonsteroidal Anti-Inflammatory Drugs by Curnock, A P, Robson, P A, Yea, C M, Moss, D, Gadher, S, Thomson, T A, Westwood, R, Ruuth, E, Williamson, R A

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Development and characterisation of tetracycline-regulated phosphoinositide 3-kinase mutants: assessing the role of multiple phosphoinositide 3-kinases in chemokine signaling: Chem... by CURNOCK, Adam P, WARD, Stephen G

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Inhibition of stimulated Jurkat cell adenosine 3′,5′-cyclic monophosphate synthesis by the immunomodulatory compound HR32577Abbreviations: PGE2, prostaglandin E2; FKN, forskolin; C... by Curnock, Adam P., Thomson, T.Andrew, Westwood, Robert, Kuo, Elizabeth A., Williamson, Richard A., Yea, Christopher M., Ruuthb, Erik

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