Anti-inflammatory Effect of a Cell-Penetrating Peptide Targeting the Nrf2/Keap1 Interaction von Steel, Richard, Cowan, Jonathan, Payerne, Estelle, O'Connell, Maria A, Searcey, Mark

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IS4‐FAM, a fluorescent tool to study CXCR4 affinity and competitive antagonism in native cancer cells von Hamshaw, Isabel, Cominetti, Marco M. D., Nana‐Akyin, Princess, Yee Ho, Ernie Ho, Searcey, Mark, Mueller, Anja

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The isolation, total synthesis and structure elucidation of chlorofusin, a natural product inhibitor of the p53-mDM2 protein-protein interaction von Clark, Ryan C, Lee, Sang Yeul, Searcey, Mark, Boger, Dale L

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Active targeting of gold nanoparticles as cancer therapeutics von Goddard, Zoë Rachael, Marín, María J., Russell, David A., Searcey, Mark

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Design and synthesis of threading intercalators to target DNA von Howell, Lesley A., Gulam, Rosul, Mueller, Anja, O’Connell, Maria A., Searcey, Mark

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Junctions in DNA: underexplored targets for therapeutic intervention von Ivens, Eleanor, Cominetti, Marco M.D., Searcey, Mark

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Ligand Bridging of the DNA Holliday Junction: Molecular Recognition of a Stacked-X Four-Way Junction by a Small Molecule von Brogden, Anna L., Hopcroft, Nicholas H., Searcey, Mark, Cardin, Christine J.

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Advances in triterpene drug discovery von Goddard, Zoë R, Searcey, Mark, Osbourn, Anne

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X-ray crystallographic study of DNA duplex cross-linking: simultaneous binding to two d(CGTACG)₂ molecules by a bis(9-aminoacridine-4-carboxamide) derivative von Hopcroft, Nicholas H, Brogden, Anna L, Searcey, Mark, Cardin, Christine J

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Borylation iridium catalysed C-H activation: a new concise route to duocarmycin derivatives von Cominetti, Marco M. D, Goddard, Zoë R, Hood, Bethany R, Beekman, Andrew M, O'Connell, Maria A, Searcey, Mark

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Perfluoroarene-based peptide macrocycles that inhibit the Nrf2/Keap1 interaction von Steel, Richard J., O'Connell, Maria A., Searcey, Mark

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The development of potent, competitive CXCR4 antagonists for the prevention of cancer metastasis von Hamshaw, Isabel, Cominetti, Marco M.D., Lai, Wing-Yee, Searcey, Mark, Mueller, Anja

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Synthesis of distamycin A polyamides targeting G-quadruplex DNA von Moore, Michael J B, Cuenca, Francisco, Searcey, Mark, Neidle, Stephen

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Structural Basis of the Negative Allosteric Modulation of 5-BDBD at Human P2X4 Receptors von Bidula, Stefan, Nadzirin, Izzuddin Bin, Cominetti, Marco, Hickey, Harry, Cullum, Sean A., Searcey, Mark, Schmid, Ralf, Fountain, Samuel J.

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Light-activated azobenzene peptide inhibitor of the PD-1/PD-L1 interaction von Hayward, Deanne, Goddard, Zoë R, Cominetti, Marco M. D, Searcey, Mark, Beekman, Andrew M

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Borylation via iridium catalysed C-H activation: a new concise route to duocarmycin derivatives von Cominetti, Marco M D, Goddard, Zoë R, Hood, Bethany R, Beekman, Andrew M, O'Connell, Maria A, Searcey, Mark

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Suramin analogues protect cartilage against osteoarthritic breakdown by increasing levels of tissue inhibitor of metalloproteinases 3 (TIMP-3) in the tissue von Green, Jonathan, Tinson, Ryan A.J., Betts, Jacob H.J., Piras, Monica, Pelut, Aylin, Steverding, Dietmar, Wren, Stephen P., Searcey, Mark, Troeberg, Linda

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Efficient Solid-Phase-Based Total Synthesis of the Bisintercalator TANDEM von Malkinson, John P, Anim, Michael K, Zloh, Mire, Searcey, Mark, Hampshire, Andrew J, Fox, Keith R

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Cytotoxicity of Pyrazine-Based Cyclometalated (C^Npz^C)Au(III) Carbene Complexes: Impact of the Nature of the Ancillary Ligand on the Biological Properties von Bertrand, Benoît, Fernandez-Cestau, Julio, Angulo, Jesus, Cominetti, Marco M. D, Waller, Zoë A. E, Searcey, Mark, O’Connell, Maria A, Bochmann, Manfred

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Taspine is a natural product that suppresses P2X4 receptor activity via phosphoinositide 3‐kinase inhibition von Nadzirin, Izzuddin Bin, Fortuny‐Gomez, Anna, Ngum, Neville, Richards, David, Ali, Seema, Searcey, Mark, Fountain, Samuel J.

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