Therapeutic dosing of an orally active, selective cathepsin S inhibitor suppresses disease in models of autoimmunity by Baugh, Mark, Black, Darcey, Westwood, Paul, Kinghorn, Emma, McGregor, Kieran, Bruin, John, Hamilton, William, Dempster, Maureen, Claxton, Christopher, Cai, Jiaqiang, Bennett, Jonathan, Long, Clive, Mckinnon, Heather, Vink, Paul, Hoed, Leontien den, Gorecka, Monika, Vora, Kalpit, Grant, Ethan, Percival, M. David, Boots, A. Mieke H, van Lierop, Marie-José

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Trifluoromethylphenyl as P2 for ketoamide-based cathepsin S inhibitors by Cai, Jiaqiang, Robinson, John, Belshaw, Simone, Everett, Kathryn, Fradera, Xavier, van Zeeland, Mario, van Berkom, Leon, van Rijnsbergen, Peter, Popplestone, Lucy, Baugh, Mark, Dempster, Maureen, Bruin, John, Hamilton, William, Kinghorn, Emma, Westwood, Paul, Kerr, Jennifer, Rankovic, Zoran, Arbuckle, Wullie, Bennett, D. Jonathan, Jones, Philip S., Long, Clive, Martin, Iain, Uitdehaag, Joost C.M., Meulemans, Tommi

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Design and optimization of a series of novel 2-cyano-pyrimidines as cathepsin K inhibitors by Rankovic, Zoran, Cai, Jiaqiang, Kerr, Jennifer, Fradera, Xavier, Robinson, John, Mistry, Ashvin, Hamilton, Emma, McGarry, George, Andrews, Fiona, Caulfield, Wilson, Cumming, Iain, Dempster, Maureen, Waller, John, Scullion, Paul, Martin, Iain, Mitchell, Ann, Long, Clive, Baugh, Mark, Westwood, Paul, Kinghorn, Emma, Bruin, John, Hamilton, William, Uitdehaag, Joost, Zeeland, Mario van, Potin, Dominique, Saniere, Laurent, Fouquet, Andre, Chevallier, François, Deronzier, Hortense, Dorleans, Cecile, Nicolai, Eric

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4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically important by Cai, Jiaqiang, Fradera, Xavier, van Zeeland, Mario, Dempster, Maureen, Cameron, Kenneth S., Bennett, D. Jonathan, Robinson, John, Popplestone, Lucy, Baugh, Mark, Westwood, Paul, Bruin, John, Hamilton, William, Kinghorn, Emma, Long, Clive, Uitdehaag, Joost C.M.

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1H-Imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors: Separation of desired cellular activity from undesired tissue accumulation through optimization of basic nitroge... by Arbuckle, Wullie, Baugh, Mark, Belshaw, Simone, Bennett, D. Jonathan, Bruin, John, Cai, Jiaqiang, Cameron, Kenneth S, Claxton, Chris, Dempster, Maureen, Everett, Kathryn, Fradera, Xavier, Hamilton, William, Jones, Philip S, Kinghorn, Emma, Long, Clive, Martin, Iain, Robinson, John, Westwood, Paul

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6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors by Cai, Jiaqiang, Baugh, Mark, Black, Darcey, Long, Clive, Jonathan Bennett, D., Dempster, Maureen, Fradera, Xavier, Gillespie, Jonathan, Andrews, Fiona, Boucharens, Sylviane, Bruin, John, Cameron, Kenneth S., Cumming, Iain, Hamilton, William, Jones, Philip S., Kaptein, Allard, Kinghorn, Emma, Maidment, Maurice, Martin, Iain, Mitchell, Ann, Rankovic, Zoran, Robinson, John, Scullion, Paul, Uitdehaag, Joost C.M., Vink, Paul, Westwood, Paul, van Zeeland, Mario, van Berkom, Leon, Bastiani, Martijn, Meulemans, Tommi

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1H-Imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors: Separation of desired cellular activity from undesired tissue accumulation through optimization of basic nitroge... by Arbuckle, Wullie, Baugh, Mark, Belshaw, Simone, Bennett, DJonathan, Bruin, John, Cai, Jiaqiang, Cameron, Kenneth S, Claxton, Chris, Dempster, Maureen, Everett, Kathryn, Fradera, Xavier, Hamilton, William, Jones, Philip S, Kinghorn, Emma, Long, Clive, Martin, Iain, Robinson, John, Westwood, Paul

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1 H-Imidazo[4,5- c]pyridine-4-carbonitrile as cathepsin S inhibitors: Separation of desired cellular activity from undesired tissue accumulation through optimization of basic nitro... by Arbuckle, Wullie, Baugh, Mark, Belshaw, Simone, Bennett, D. Jonathan, Bruin, John, Cai, Jiaqiang, Cameron, Kenneth S., Claxton, Chris, Dempster, Maureen, Everett, Kathryn, Fradera, Xavier, Hamilton, William, Jones, Philip S., Kinghorn, Emma, Long, Clive, Martin, Iain, Robinson, John, Westwood, Paul

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2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitors by Cai, Jiaqiang, Bennett, D. Jonathan, Rankovic, Zoran, Dempster, Maureen, Fradera, Xavier, Gillespie, Jonathan, Cumming, Iain, Finlay, William, Baugh, Mark, Boucharens, Sylviane, Bruin, John, Cameron, Kenneth S., Hamilton, William, Kerr, Jennifer, Kinghorn, Emma, McGarry, George, Robinson, John, Scullion, Paul, Uitdehaag, Joost C.M., van Zeeland, Mario, Potin, Dominique, Saniere, Laurent, Fouquet, Andre, Chevallier, Francois, Deronzier, Hortense, Dorleans, Cecile, Nicolai, Eric

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Parallel solid-phase synthesis of zatebradine analogues as potential If channel blockers by BOM, Anton, BOOTH, Susan, BRUIN, John, CLARK, John, MILLER, Susan, WATHEY, Bernard

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Parallel solid-Phase synthesis of zatebradine analogues as potential I f channel blockers by Bom, Anton, Booth, Susan, Bruin, John, Clark, John, Miller, Susan, Wathey, Bernard

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Heidegger and Two Kinds of Art by Bruin, John

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Discussion: Heidegger and The World of The Work of Art by BRUIN, JOHN

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Heidegger and the World of the Work of Art by Bruin, John

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Heidegger and Two Kinds of Art by Bruin, John

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Modulation of the immune system in the mouse. 2. Drug administration following antigen sensitization by Cottney, Jean, Bruin, John, Lewis, Alan J.

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Lyric philosophy by Bruin, John

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Lyric philosophy: Jan Zwicky (Toronto: University of Toronto Press, 1993), Toronto Studies in Philosophy, xvii + 566 pp., £16.95/28.00 paper, £42.00/£71.00 cloth by Bruin, John

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"Lyric Philosophy", Jan Zwicky (Book Review) by Bruin, John

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Modulation of the immune system in the mouse 1. Drug administration prior to antien sensitization by Cottney, Jean, Bruin, John, Lewis, Alan J.

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