An in situ combinatorial methodology to synthesize and screen chemical probes von van der Zouwen, Antonie J, Lohse, Jonas, Wieske, Lianne H E, Hohmann, Katharina F, van der Vlag, Ramon, Witte, Martin D

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The linkage-type and the exchange molecule affect the protein-labeling efficiency of iminoboronate probes von van der Zouwen, Antonie J, Jeucken, Aike, van der Pol, Elske, Boerema, Gerben, Slotboom, Dirk J, Witte, Martin D

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Iminoboronates as Dual‐Purpose Linkers in Chemical Probe Development von Zouwen, Antonie J., Jeucken, Aike, Steneker, Roy, Hohmann, Katharina F., Lohse, Jonas, Slotboom, Dirk J., Witte, Martin D.

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Robust proteome profiling of cysteine-reactive fragments using label-free chemoproteomics von Biggs, George S., Cawood, Emma E., Vuorinen, Aini, McCarthy, William J., Wilders, Harry, Riziotis, Ioannis G., van der Zouwen, Antonie J., Pettinger, Jonathan, Nightingale, Luke, Chen, Peiling, Powell, Andrew J., House, David, Boulton, Simon J., Skehel, J. Mark, Rittinger, Katrin, Bush, Jacob T.

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Modular Approaches to Synthesize Activity- and Affinity-Based Chemical Probes von van der Zouwen, Antonie J, Witte, Martin D

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Covalent fragment-based drug discovery for target tractability von McCarthy, William J., van der Zouwen, Antonie J., Bush, Jacob T., Rittinger, Katrin

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An in situ combinatorial methodology to synthesize and screen chemical probesElectronic supplementary information (ESI) available: Supplementary figures and tables, experimental pr... von van der Zouwen, Antonie J, Lohse, Jonas, Wieske, Lianne H. E, Hohmann, Katharina F, van der Vlag, Ramon, Witte, Martin D

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