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conditions (3aR,4S,8S,12R,12aS,12bR)-10-methyl-2-phenyloctahydro-1H-4,12a-etheno-8,12-methanopyrrolo[3

Thymidylate synthase (ThS) is a target for antimetabolite antitumor drugs. Such drugs have been

SHITARA, K., OHTSU, A., ÖZGÜROĞLU, M., BANG, Y.J., DI BARTOLOMEO, M., MANDALÀ, M., RYU, M.H.., FORNARO, L., OLESIŃSKI, T., CAGLEVIC, C., CHUNG, H.C., MURO, K., GOEKKURT, E., MANSOOR, W., MCDERMOTT, R.S., SHACHAM-SHMUELI, E., CHEN, X., MAYO, C., KANG, S.P., FUCHS, C.S., LERZO, G., O'CONNOR, J.M., MENDEZ, G.A., LYNAM, J., TEBBUTT, N., WONG, M., STRICKLAND, A., KARAPETIS, C., GOLDSTEIN, D., VASEY, P., VAN LAETHEM, J.L., VAN CUTSEM, E., BERRY, S., VINCENT, M., MULLER, B., REY, F., ZAMBRANO, A., GUERRA, J., KROGH, M., BAEKSGAARD, L., YILMAZ, M., ELME, A., MAGI, A., AUVINEN, P., ALANKO, T., MOEHLER, M., KUNZMANN, V., SEUFFERLEIN, T., THUSS-PATIENCE, P., HOEHLER, T., HAAG, G., AL-BATRAN, S.E., CASTRO, H., LOPEZ, K., AGUILAR VASQUEZ, M., SANDOVAL, M., LAM, K.O., CUFFE, S., KELLY, C., GEVA, R., HUBERT, A., BENY, A., BRENNER, B., GIUSEPPE, A., FALCONE, A., MAIELLO, E., PASSALACQUA, R., MONTESARCHIO, V., HARA, H., CHIN, K., NISHINA, T., KOMATSU, Y., MACHIDA, N., HIRONAKA, S., SATOH, T., TAMURA, T., SUGIMOTO, N., CHO, H., OMURO, Y., KATO, K., GOTO, M., HYODO, I., YOSHIDA, K., BABA, H., ESAKI, T., FURUSE, J., WAN MOHAMMED, W.Z., HERNANDEZ HERNANDEZ, C., CASAS GARCIA, J., DOMINGUEZ ANDRADE, A., CLARKE, K., HJORTLAND, G., GLENJEN, N., KUBIATOWSKI, T., JACEK, J., WOJTUKIEWICZ, M., LAZAREV, S., LANCUKHAY, Y., AFANASAYEV, S., MOISEYENKO, V., KOSTOROV, V., PROTSENKO, S., SHIRINKIN, V., SAKAEVA, D., FADEEVA, N., YONG, W.P., ROBERTSON, B., NG, C.H.M., ROBERTSON, B., RAPAPORT, B., COHEN, G., DREOSTI, L., RUFF, P., JACOBS, C., LANDERS, G., SZPAK, W., ROH, S.Y., LEE, J., KIM, Y.H., ALSINA MAQUEDA, M., LONGO MUNOZ, F., CERVANTES AGUILAR, A., ARANDA AGUILAR, E., GARCIA ALFONSO, P., RIVERA, F., FELIU BATLE, J., PAZO CID, R., YEH, K.H., CHEN, J.S., CHAO, Y., YEN, C.J., KARA, O., YALCIN, S., HOCHHAUSER, D., CHAU, I., BENSON, A., SHANKARAN, V., SHAIB, W., PHILIP, P., SHARMA, V., SIEGEL, R., SUN, W., WAINBERG, Z., GEORGE, B., BULLOCK, A., MYRICK, S., FARUOL, J., LARSON, T., BECERRA, C., RATNAM, S., RICHARDS, D.A., RICHE, S.L (2018)
or gastrooesophageal junction cancer that progressed on first-line chemotherapy with a platinum and fluoropyrimidine


ETIOPATHOGENETIC FEATURES OF THE FURUNCLE OF THE MAXILLOFACIAL REGIONThe objects were 45 patients with a furuncle of the maxillofacial region (FMFR). The polymorphism

A2:1 β-cyclodextrin – histochrome complex was synthesized based on a comparison with experimental



-cyanoethyl derivatives. The reaction with 3,11-dioxo analog afforded 2,2-disubstituted derivative as a result

. CONCLUSIONS A+AVD had superior efficacy to ABVD in the treatment of patients with advanced-stage Hodgkin’s

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