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Chemical Society Reviews|July 12, 2019
Cleavable linkers in antibody-drug conjugatesJonathan D Bargh, Albert Isidro-Llobet, Jeremy S Parker, et al.Chemical Communications (Cambridge, England)|March 9, 2021
A dual-enzyme cleavable linker for antibody-drug conjugatesJonathan D Bargh, Stephen J Walsh, Nicola Ashman, et al.Chemical Science|June 4, 2021
Sulfatase-cleavable linkers for antibody-drug conjugatesJonathan D Bargh, Stephen J Walsh, Albert Isidro-Llobet, et al.Chemical Science|July 19, 2021
Rapid and robust cysteine bioconjugation with vinylheteroarenesHikaru Seki, Stephen J Walsh, Jonathan D Bargh, et al.Nature Communications|September 25, 2010
Diversity-oriented synthesis as a tool for the discovery of novel biologically active small moleculesWarren R J D Galloway, Albert Isidro-Llobet, David R SpringChemical Society Reviews|December 8, 2020
Site-selective modification strategies in antibody-drug conjugatesStephen J Walsh, Jonathan D Bargh, Friederike M Dannheim, et al.Chemical Society Reviews|November 2, 2022
Non-internalising antibody-drug conjugatesNicola Ashman, Jonathan D Bargh, David R SpringAngewandte Chemie (International Ed. in English)|January 13, 2009
Synthesis of unprecedented scaffold diversityWarren R J D Galloway, Mónica Diáz-Gavilán, Albert Isidro-Llobet, et al.Organic & Biomolecular Chemistry|May 21, 2020
General dual functionalisation of biomacromolecules via a cysteine bridging strategyStephen J Walsh, Jessica Iegre, Hikaru Seki, et al.Chemical Science|August 17, 2022
All-in-one disulfide bridging enables the generation of antibody conjugates with modular cargo loadingFriederike M Dannheim, Stephen J Walsh, Carolina T Orozco, et al.Pageof 26