Zobrazeno 1 - 10
of 42
pro vyhledávání: '"J J, Starling"'
Autor:
N, Suh, A L, Glasebrook, A D, Palkowitz, H U, Bryant, L L, Burris, J J, Starling, H L, Pearce, C, Williams, C, Peer, Y, Wang, M B, Sporn
Publikováno v:
Cancer research. 61(23)
Arzoxifene ([6-hydroxy-3-[4-[2-(1-piperidinyl)-ethoxy]phenoxy]-2-(4-methoxyphenyl)]benzo[b]thiophene) is a selective estrogen receptor modulator (SERM) that is a potent estrogen antagonist in mammary and uterine tissue while acting as an estrogen ago
Publikováno v:
Current medicinal chemistry. 8(1)
Multidrug resistance may be conferred by P-glycoprotein (Pgp, ABCB1) or the multidrug resistance associated protein (MRP). These membrane proteins are members of the ATP binding cassette transporter superfamily and are responsible for the removal fro
Autor:
A H, Dantzig, R L, Shepard, K L, Law, L, Tabas, S, Pratt, J S, Gillespie, S N, Binkley, M T, Kuhfeld, J J, Starling, S A, Wrighton
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 290(2)
Overexpression of ATP-dependent drug efflux pumps, P-glycoprotein (Pgp) or multidrug resistance-associated protein (MRP), confers multidrug resistance to tumor cells. Modulators of multidrug resistance block the action of these pumps, thereby sensiti
Autor:
A H, Dantzig, R L, Shepard, J, Cao, K L, Law, W J, Ehlhardt, T M, Baughman, T F, Bumol, J J, Starling
Publikováno v:
Cancer research. 56(18)
Overexpression of P-glycoprotein (Pgp) by tumors results in multidrug resistance (MDR) to structurally unrelated oncolytics. MDR cells may be sensitized to these oncolytics when treated with a Pgp modulator. The present study evaluates LY335979 as a
Autor:
V F, Patel, J N, Hardin, J M, Mastro, K L, Law, J L, Zimmermann, W J, Ehlhardt, J M, Woodland, J J, Starling
Publikováno v:
Bioconjugate chemistry. 7(4)
LY207702 (1) is a difluorinated purine nucleoside that exhibits impressive antitumor activity in preclinical models. This agent, however, also possesses cardiotoxicity which limits the potential clinical utility of this novel drug candidate. We there
Publikováno v:
Anticancer research. 14(3A)
Well established UCLA-P3 human lung tumor xenografts were significantly regressed by treatment with a monoclonal antibody-vinca immunoconjugate whereas no regressions were observed for the LS174T and SW948 human colon carcinoma xenografts by this the
Publikováno v:
Cancer research. 51(11)
It is widely believed that antigen heterogeneity and noninternalization of antigen-antibody complexes will severely limit the antitumor activity of monoclonal antibody-drug conjugates. The B72.3 monoclonal antibody binds to a tumor-associated antigen
Autor:
J J, Starling, R S, Maciak, N A, Hinson, J, Hoskins, B C, Laguzza, R A, Gadski, J, Strnad, L, Rittmann-Grauer, S V, DeHerdt, T F, Bumol
Publikováno v:
Cancer research. 50(23)
UCLA-P3 human lung adenocarcinoma cells were grown in nude mice and given repetitive treatments of a monoclonal antibody-Vinca alkaloid immunoconjugate. Although this therapy resulted in a greater than 4-fold reduction in mean tumor mass of the estab
Publikováno v:
The Prostate. 3:203-214
Antibodies against a soluble cytoplasmic protein contained in prostate epithelial cells were developed using the hybridoma technique. This was done to provide markers for these cells that can be used to identify acinar cells in culture and to follow
Publikováno v:
The Prostate. 6:205-215
Virological and epidemiological studies have implicated human cytomegalovirus (HCMV) as a possible etiological agent of prostate cancer. Because of the suspected associations, this laboratory tested the reactivity of a prostate-associated monoclonal