Zobrazeno 1 - 10
of 11
pro vyhledávání: '"W G, Bornmann"'
Publikováno v:
ract. 77:87-89
Autor:
T, Gilewski, G, Ragupathi, S, Bhuta, L J, Williams, C, Musselli, X F, Zhang, W G, Bornmann, M, Spassova, K P, Bencsath, K S, Panageas, J, Chin, C A, Hudis, L, Norton, A N, Houghton, P O, Livingston, S J, Danishefsky
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 98(6)
The carbohydrate antigen globo H commonly found on breast cancer cells is a potential target for vaccine therapy. The objectives of this trial were to determine the toxicity and immunogenicity of three synthetic globo H-keyhole limpet hemocyanin conj
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(9)
Earlier studies from this laboratory have shown that the uricosuric agent probenecid (PBCD) will inhibit the extrusion of folate analogues from tumor cells mediated by a plasma membrane ATPase resembling the canicular multispecific organic anion tran
Autor:
W. G. Bornmann, David A. Boothman, John J. Pink, Sarah M. Planchon, Shelly M. Wuerzberger-Davis, K. A. Robertson
Publikováno v:
Oncology reports. 6(3)
We previously demonstrated that beta-lapachone (beta-lap) killed cancer cells solely by apoptosis. Beta-Lap induced apoptosis in HL-60 cells in a dose-dependent manner as measured by flow cytometry and DNA ladder formation. Cell cycle changes, such a
Schedule-dependent synergism between raltitrexed and irinotecan in human colon cancer cells in vitro
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 4(5)
The quinazoline folate analogue raltitrexed (ZD1694; Tomudex) and the camptothecin derivative irinotecan are two new agents showing clinical activity against colorectal cancer. To identify the optimal conditions to achieve synergistic cytotoxicity be
Publikováno v:
Cancer research. 58(9)
Beta-lapachone (beta-lap) affects a number of enzymes in vitro, including type I topoisomerase (Topo I); however, its exact intracellular target(s) and mechanism of cell killing remain unknown. We compared the cytotoxic responses of MCF-7:WS8 (MCF-7)
Publikováno v:
Molecular pharmacology. 48(1)
Oltipraz, an inhibitor of human immunodeficiency virus type 1 replication in vitro (ED50 approximately 10 microM), undergoes extensive metabolism in vivo. Most of the orally administered drug undergoes opening of the dithiolethione ring, reduction, r
Autor:
C K, Joseph, S D, Wright, W G, Bornmann, J T, Randolph, E R, Kumar, R, Bittman, J, Liu, R N, Kolesnick
Publikováno v:
The Journal of biological chemistry. 269(26)
Bacterial lipopolysaccharide (LPS), tumor necrosis factor (TNF)-alpha and interleukin-1 beta (IL-1 beta) stimulate similar cellular responses. TNF-alpha and IL-1 beta are known to initiate signaling through a pathway involving hydrolysis of sphingomy
Autor:
B. P. MUNDY, W. G. BORNMANN
Publikováno v:
Chemischer Informationsdienst. 16
Autor:
M. E. KUEHNE, J. C. BOHNERT, W. G. BORNMANN, C. L. KIRKEMO, S. E. KUEHNE, P. J. SEATON, T. C. ZEBOVITZ
Publikováno v:
Chemischer Informationsdienst. 16