New therapeutic targets for the treatment of high-risk neuroblastoma von Wagner, Lars M., Danks, Mary K.

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Development of a tumor-selective approach to treat metastatic cancer von Aboody, Karen S, Bush, Rebecca A, Garcia, Elizabeth, Metz, Marianne Z, Najbauer, Joseph, Justus, Kristine A, Phelps, Doris A, Remack, Joanna S, Yoon, Karina Jin, Gillespie, Shanna, Kim, Seung U, Glackin, Carlotta A, Potter, Philip M, Danks, Mary K

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Stem and progenitor cell-mediated tumor selective gene therapy von Aboody, K S, Najbauer, J, Danks, M K

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Identification and Characterization of Novel Benzil (Diphenylethane-1,2-dione) Analogues as Inhibitors of Mammalian Carboxylesterases von Wadkins, Randy M, Hyatt, Janice L, Wei, Xin, Yoon, Kyoung Jin P, Wierdl, Monika, Edwards, Carol C, Morton, Christopher L, Obenauer, John C, Damodaran, Komath, Beroza, Paul, Danks, Mary K, Potter, Philip M

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Stem and progenitor cell-mediated tumor selective gene therapy von Aboody, K S, Najbauer, J, Danks, M K

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Tumor-targeted enzyme/prodrug therapy mediates long-term disease-free survival of mice bearing disseminated neuroblastoma von DANKS, Mary K, YOON, K. Jin, POTTER, Philip M, ABOODY, Karen S, BUSH, Rebecca A, REMACK, Joanna S, WIERDL, Monika, TSURKAN, Lyudmila, KIM, Seung U, GARCIA, Elizabeth, METZ, Marianne Z, NAJBAUER, Joseph

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Towards a common purpose: a theoretical model for a whole system approach to physical activity developed in South Tees von Danks, K, Shearn, K, Dalkin, S, Fitzgerald, M, Broom, DR

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Cell adhesion molecules as targets for therapy of neuroblastoma von Yoon, Karina Jin, Danks, Mary K.

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Selective Inhibition of Carboxylesterases by Isatins, Indole-2,3-diones von Hyatt, Janice L, Moak, Teri, Hatfield, M. Jason, Tsurkan, Lyudmila, Edwards, Carol C, Wierdl, Monika, Danks, Mary K, Wadkins, Randy M, Potter, Philip M

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Discovery of Novel Selective Inhibitors of Human Intestinal Carboxylesterase for the Amelioration of Irinotecan-Induced Diarrhea: Synthesis, Quantitative Structure-Activity Relatio... von Wadkins, Randy M, Hyatt, Janice L, Yoon, Kyoung Jin P, Morton, Christopher L, Lee, Richard E, Damodaran, Komath, Beroza, Paul, Danks, Mary K, Potter, Philip M

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Proficient metabolism of irinotecan by a human intestinal carboxylesterase von KHANNA, Ruchi, MORTON, Christopher L, DANKS, Mary K, POTTER, Philip M

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Efficacy of topoisomerase I inhibitors, topotecan and irinotecan, administered at low dose levels in protracted schedules to mice bearing xenografts of human tumors von HOUGHTON, P. J, CHESHIRE, P. J, HALLMAN, J. D, LUTZ, L, FRIEDMAN, H. S, DANKS, M. K, HOUGHTON, J. A

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Activation and antitumor activity of CPT-11 in plasma esterase-deficient mice von MORTON, Christopher L, IACONO, Lisa, HYATT, Janice L, TAYLOR, Kody R, CHESHIRE, Pamela J, HOUGHTON, Peter J, DANKS, Mary K, STEWART, Clinton F, POTTER, Philip M

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Structural insights into CPT-11 activation by mammalian carboxylesterases von Redinbo, Matthew R, Bencharit, Sompop, Morton, Christopher L, Howard-Williams, Escher L, Danks, Mary K, Potter, Philip M

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Brain tumor oncolysis with replication-conditional herpes simplex virus type 1 expressing the prodrug-activating genes, CYP2B1 and secreted human intestinal carboxylesterase, in co... von Tyminski, Edyta, Leroy, Stanley, Terada, Kinya, Finkelstein, Dianne M, Hyatt, Janice L, Danks, Mary K, Potter, Philip M, Saeki, Yoshinaga, Chiocca, E Antonio

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Planarity and Constraint of the Carbonyl Groups in 1,2-Diones Are Determinants for Selective Inhibition of Human Carboxylesterase 1 von Hyatt, Janice L, Wadkins, Randy M, Tsurkan, Lyudmila, Hicks, Latorya D, Hatfield, M. Jason, Edwards, Carol C, Ross, Charles R, Cantalupo, Stephanie A, Crundwell, Guy, Danks, Mary K, Guy, R. Kip, Potter, Philip M

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Studies on the Mechanism of Resistance to Rapamycin in Human Cancer Cells von Hosoi, H, Dilling, M B, Liu, L N, Danks, M K, Shikata, T, Sekulic, A, Abraham, R T, Lawrence, Jr, J C, Houghton, P J

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Intracellular inhibition of carboxylesterases by benzil: modulation of CPT-11 cytotoxicity von Hyatt, Janice L, Tsurkan, Lyudmila, Wierdl, Monika, Edwards, Carol C, Danks, Mary K, Potter, Philip M

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The anticancer prodrug CPT-11 is a potent inhibitor of acetylcholinesterase but is rapidly catalyzed to SN-38 by butyrylcholinesterase von MORTON, C. L, WADKINS, R. M, DANKS, M. K, POTTER, P. M

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Comparison of Activation of CPT-11 by Rabbit and Human Carboxylesterases for Use in Enzyme/Prodrug Therapy von DANKS, M. K, MORTON, C. L, KRULL, E. J, CHESHIRE, P. J, RICHMOND, L. B, NAEVE, C. W, PAWLIK, C. A, HOUGHTON, P. J, POTTER, P. M

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