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Активация ооцитов: фундаментальные и клинические аспекты кальция в клетке при участии специфической фосфолипазы C ζ, фермента сперматозоидов, вводимого в ооплазму


were identified in the CRYAA gene: c.253C > T (p.L85F) in one family and c.291C > G (p.H97Q) in two


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)

, and that there is an association of hereditary BC and mutations c.1321G>A in MLH1, c.260C>G and c.2178G>C in MSH2, c.3217C>T in MSH


a, miR-34b, miR-449v, miR-449c as markers of male infertility and to evaluate the dependence

of polymorphic variants of inflammation genes with MetS and serum levels of high-sensitivity C-reactive protein

3129934 (C6orf10), rs1109670 (DDEF2/MBOAT2 gene), rs9523762 (GPC5 gene), rs28362491 (NFKB1 gene), rs

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