Zobrazeno 1 - 10
of 213
pro vyhledávání: '"I. Umezawa"'
Publikováno v:
ChemInform. 24
Publikováno v:
Drug design and discovery. 16(3)
A useful calmodulin (CaM) antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7), was invented by Hidaka et al. in 1978 (J. Pharmacol. Exp. Ther. 207, 8-15). Here, we have designed new CaM antagonists on the basis of the three-dimension
Autor:
Robert J. Linhardt, E. A. Balazs, D. J. Wedlock, G. O. Phillips, A. Leshchiner, R. S. Langer, R. J. Linhardt, C. L. Cooney, G. Fitzgerald, A. Grant, S. E. Lasker, J. C. Lormeau, J. Choay, J. Goulay, M. T. Goulay-Heir, M. A. Goulay-Heir, G. Goulay-Heir, M. Petitou, D. B. Soll, S. E. Harrison, L. L. Teng, A. G. Walton, R. V. Sparer, N. Ekwuribe, J. K. Borchardt, J. W. Bracke, K. Thacker, P. Brocklehurst, A. S. Ferguson, L. K. Gordon, H. Hayes, S. Inoue, H. Yamamoto, A. M. Nonomura, R. Pappo, J. M. Schweid, A. H. Cohee, A. F. Dec, L. K. Shay, S. E. Reiter, L. Turrisi, I. Umezawa, K. Komiyama, D. Williams, D. M. Munnecke, R. T. Zahradnik, K. Arizono, M. Terasawa, M. Nobutoki, L. C. A. Bergwitz, R. G. L. Osterlund, C. Brain, B. Johnston, L. G. Brooker, T. S. Chang, L. J. Zientek, A. Viniguaz, I. Chibata, T. Tosa, S. Takamatsu, D. F. Doehnert, A. S. Hill, D. P. Gaehring, J. V. Scanlon, G. D. Hansen, K. M. E. Hellsten, R. L. Horion, R. B. Kennedy, R. S. Kohn, A. J. Kruger, J. K. Johnson, W. Y. Kuu, V. K. Larsson, J. F. Mezzino, L. Y. Chuang, J. Michnowski, Y. Miyashiro, M. Ogawa, Y. Yamazaki, S. Igarasi, K. Morimoto, S. Nochumson, M. A. Pellico, R. J. Purinton, F. Reinhardt, K. Sakata, H. Imai, A. J. Sensabaugh, D. C. Crepps, W. Y. Rice, G. W. Fearrington, J. L. Shim, Y. Shimohiro, T. Ohnishi, E. Simon, H. Stuhler, E. Krempl, D. T. Su, K. Szendrei, E. Minker, Z. Re, L. Koch, L. Wolf, E. Szijj, M. Re, M. Trop, D. C. Tunc, T. Ueda, M. Vellini, R. B. Wallace, K. Watanabe, S. Yoshikawa, S. Futami, R. H. Wunder
Publikováno v:
Applied Biochemistry and Biotechnology. 12:177-197
Publikováno v:
Gan. 72(1)
The antitumor activity of a new derivative of nitrosourea, 3-[3-(2-chloroethyl)-3-nitrosoureido]-3-deoxy-D-glucopyranose (CNUG), against murine tumors was studied. CNUG showed remarkable antitumor activity against leukemias L1210 and P388, Lewis lung
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 15(5)
Antitumor activity of Juzen-Taiho-Toh (JTX) and combination effect of JTX with antitumor agents were studied using murine tumors. In order to determine the antitumor activity of JTX, mice inoculated ip with IMC carcinoma (1 X 10(6) cells/CDF1 mouse),
Publikováno v:
The Kitasato archives of experimental medicine. 60(3)
Publikováno v:
Gan. 72(4)
The role of immunological effects in the antitumor activity of sporamycin activity of sporamycin was studied mainly using the mouse syngeneic tumor, Meth-A. Sporamycin inhibited the growth of the Meth-A tumor and Balb/c mice, and 12 out of 19 mice we
Publikováno v:
SPIE Proceedings.
Recent research and development work on AlGaInP visible laser diodes by SONY are reviewed. Performance and reliability of a gain-guided 670 nm laser with a tapered geometry are described. Efforts for achieving shorter wavelengths around 650 nm with u
Publikováno v:
The Japanese journal of antibiotics. 35(12)
Publikováno v:
Gan. 70(3)
Transplacental induction of lung tumor by 1-ethyl-1-nitrosourea (ENU) was studied in pregnant ddY mice which were given a single intraperitoneal injection of 58.5 mg/kg of ENU in water between day 13 and 19 of gestation. Within 4 approximately 6 week