Metal compounds for the treatment of parasitic diseases von Fricker, Simon P., Mosi, Renee M., Cameron, Beth R., Baird, Ian, Zhu, Youngbao, Anastassov, Virginia, Cox, Jennifer, Doyle, Patricia S., Hansell, Elizabeth, Lau, Gloria, Langille, Jonathan, Olsen, Micki, Qin, Ling, Skerlj, Renato, Wong, Rebecca S.Y., Santucci, Zefferino, McKerrow, James H.

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Characterization of the molecular pharmacology of AMD3100: A specific antagonist of the G-protein coupled chemokine receptor, CXCR4 von Fricker, Simon P., Anastassov, Virginia, Cox, Jennifer, Darkes, Marilyn C., Grujic, Ognjen, Idzan, Stefan R., Labrecque, Jean, Lau, Gloria, Mosi, Renee M., Nelson, Kim L., Qin, Ling, Santucci, Zeffy, Wong, Rebecca S.Y.

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The molecular pharmacology of AMD11070: An orally bioavailable CXCR4 HIV entry inhibitor von Mosi, Renee M., Anastassova, Virginia, Cox, Jennifer, Darkes, Marilyn C., Idzan, Stefan R., Labrecque, Jean, Lau, Gloria, Nelson, Kim L., Patel, Ketan, Santucci, Zefferino, Wong, Rebecca S.Y., Skerlj, Renato T., Bridger, Gary J., Huskens, Dana, Schols, Dominique, Fricker, Simon P.

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Pharmacology of AMD3465: A small molecule antagonist of the chemokine receptor CXCR4 von Bodart, Veronique, Anastassov, Virginia, Darkes, Marilyn C., Idzan, Stefan R., Labrecque, Jean, Lau, Gloria, Mosi, Renee M., Neff, Kathleen S., Nelson, Kim L., Ruzek, Melanie C., Patel, Ketan, Santucci, Zefferino, Scarborough, Robert, Wong, Rebecca S.Y., Bridger, Gary J., MacFarland, Ron T., Fricker, Simon P.

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The orally bioavailable allosteric CXCR4 HIV-1 entry inhibitor AMD11070 von Fricker, Simon, Mosi, Renee, Anastassova, Virginia, Labrecque, Jean, Wong, Rebecca, Skerlj, Renato, Bridger, Gary, Huskens, Dana, Schols, Dominique

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Structures of lactate dehydrogenase A (LDHA) in apo, ternary and inhibitor-bound forms von Kolappan, Subramaniapillai, Shen, David L., Mosi, Renee, Sun, Jianyu, McEachern, Ernest J., Vocadlo, David J., Craig, Lisa

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Trapping and Characterization of the Reaction Intermediate in Cyclodextrin Glycosyltransferase by Use of Activated Substrates and a Mutant Enzyme von Mosi, Renee, He, Shouming, Uitdehaag, Joost, Dijkstra, Bauke W, Withers, Stephen G

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Inhibition of the cathepsin cysteine proteases B and K by square-planar cycloaurated gold(III) compounds and investigation of their anti-cancer activity von Zhu, Yongbao, Cameron, Beth R., Mosi, Renee, Anastassov, Virginia, Cox, Jennifer, Qin, Ling, Santucci, Zefferino, Metz, Markus, Skerlj, Renato T., Fricker, Simon P.

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Synthesis of 4-methylumbelliferyl I--d-mannopyranosyl-(1a6)-I2-d-mannopyranoside and development of a coupled fluorescent assay for GH125 exo-I--1,6-mannosidases von Deng, Lehua, Tsybina, Polina, Gregg, Katie, Mosi, Renee, Zandberg, Wesley, Boraston, Alisdair, Vocadlo, David

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Synthesis of 4-methylumbelliferyl α-d-mannopyranosyl-(1→6)-β-d-mannopyranoside and development of a coupled fluorescent assay for GH125 exo-α-1,6-mannosidases von Deng, Lehua, Tsybina, Polina, Gregg, Katie J., Mosi, Renee, Zandberg, Wesley F., Boraston, Alisdair B., Vocadlo, David J.

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Design of Substituted Imidazolidinylpiperidinylbenzoic Acids as Chemokine Receptor 5 Antagonists: Potent Inhibitors of R5 HIV‑1 Replication von Skerlj, Renato, Bridger, Gary, Zhou, Yuanxi, Bourque, Elyse, McEachern, Ernest, Metz, Markus, Harwig, Curtis, Li, Tong-Shuang, Yang, Wen, Bogucki, David, Zhu, Yongbao, Langille, Jonathan, Veale, Duane, Ba, Tuya, Bey, Michael, Baird, Ian, Kaller, Alan, Krumpak, Maria, Leitch, David, Satori, Michael, Vocadlo, Krystyna, Guay, Danielle, Nan, Susan, Yee, Helen, Crawford, Jason, Chen, Gang, Wilson, Trevor, Carpenter, Bryon, Gauthier, David, MacFarland, Ron, Mosi, Renee, Bodart, Veronique, Wong, Rebecca, Fricker, Simon, Schols, Dominique

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Rhenium Inhibitors of Cathepsin B (ReO(SYS)X (Where Y = S, py; X = Cl, Br, SPhOMe-p)):  Synthesis and Mechanism of Inhibition von Mosi, Renee, Baird, Ian R, Cox, Jennifer, Anastassov, Virginia, Cameron, Beth, Skerlj, Renato T, Fricker, Simon P

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X-ray structures along the reaction pathway of cyclodextrin glycosyltransferase elucidate catalysis in the α-amylase family von Uitdehaag, Joost C. M, Mosi, Renée, Kalk, Kor H, van der Veen, Bart A, Dijkhuizen, Lubbert, Withers, Stephen G, Dijkstra, Bauke W

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Design and synthesis of pyridin-2-ylmethylaminopiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replication von Skerlj, Renato, Bridger, Gary, Zhou, Yuanxi, Bourque, Elyse, McEachern, Ernest, Langille, Jonathan, Harwig, Curtis, Veale, Duane, Yang, Wen, Li, Tongshong, Zhu, Yongbao, Bey, Michael, Baird, Ian, Sartori, Michael, Metz, Markus, Mosi, Renee, Nelson, Kim, Bodart, Veronique, Wong, Rebecca, Fricker, Simon, Mac Farland, Ron, Huskens, Dana, Schols, Dominique

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The molecular pharmacology of AMD11070: An orally bioavailable CXCR4 HIV entry inhibitor von Mosi, Renee M, Anastassova, Virginia, Cox, Jennifer, Darkes, Marilyn C, Idzan, Stefan R, Labrecque, Jean, Lau, Gloria, Nelson, Kim L, Patel, Ketan, Santucci, Zefferino, Wong, Rebecca S.Y, Skerlj, Renato T, Bridger, Gary J, Huskens, Dana, Schols, Dominique, Fricker, Simon P

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‘3 + 1’ mixed-ligand oxorhenium(V) complexes and their inhibition of the cysteine proteases cathepsin B and cathepsin K von Baird, Ian R., Mosi, Renee, Olsen, Micki, Cameron, Beth R., Fricker, Simon P., Skerlj, Renato T.

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Trapping of α-glycosidase intermediates von Mosi, Renée M., Withers, Stephen G.

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Mitigating hERG Inhibition: Design of Orally Bioavailable CCR5 Antagonists as Potent Inhibitors of R5 HIV-1 Replication von Skerlj, Renato, Bridger, Gary, Zhou, Yuanxi, Bourque, Elyse, McEachern, Ernest, Danthi, Sanjay, Langille, Jonathan, Harwig, Curtis, Veale, Duane, Carpenter, Bryon, Ba, Tuya, Bey, Michael, Baird, Ian, Wilson, Trevor, Metz, Markus, MacFarland, Ron, Mosi, Renee, Bodart, Veronique, Wong, Rebecca, Fricker, Simon, Huskens, Dana, Schols, Dominique

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Erratum to “Metal compounds for the treatment of parasitic diseases” [J. Inorg. Biochem. 102 (2008) 1839–1845] von Fricker, Simon P., Mosi, Renee M., Cameron, Beth R., Baird, Ian, Zhu, Youngbao, Anastassov, Virginia, Cox, Jennifer, Doyle, Patricia S., Hansell, Elizabeth, Lau, Gloria, Langille, Jonathan, Olsen, Micki, Qin, Ling, Skerlj, Renato, Wong, Rebecca S.Y., Santucci, Zefferino, McKerrow, James H.

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Synthesis and kinetic evaluation of 4-deoxymaltopentaose and 4-deoxymaltohexaose as inhibitors of muscle and potato α-glucan phosphorylases von MOSI, Renee, WITHERS, Stephen G.

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