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Immunohistochemical study of expression of receptors to steroid hormones in endometrial hyperplasia. The detected zones free of receptors to estrogens and progesterone evidence for local disturbance of a

Endometrial morphological and immunohistochemical features in females with primary and secondary infertility were studied by histological and immnohistological (estrogen and progesterone receptors, Ki67) methods

Expression of steroid hormone receptors in courses of simple endometrial hyperplasia was used to study specificity of the location of estrogen and progesterone receptors in simple endometrial

Investigation of estrogen and progesterone receptors expression estimated by RT-PCR connection with proliferation and apoptotic activity in breast cancer tissueExpression of estrogen and progesterone receptors mRNA in breast cancer tissue may either rise

Involvement of estrogen and progesterone receptor gene polymorphisms in the development of uterine fibroids in the control one. Five polymorphic loci of the estrogen and progesterone receptor genes: РGR c.1415-11113G> Т

Analysis of the association between the polymorphic variants of estrogen and progesterone receptor genes and genital endometriosis and progesterone receptor genes were selected for the study: ЕSR1 с.453-397Т>С rs2234693, ЕSR1 c.1029Т>С rs3798577

Immunohistochemical reseach of estrogens and progesteron receptors at endometrial adenocarcinomas and progesterone receptors and degree of neoplastic changes in endometrial adenocarcinomas. The greatest receptors

Ulipristal acetate in leiomyomas treatment the effectiveness of the progesterone receptor modulator ulipristal acetate in the preoperative treatment

POSTMENOPAUSAL ESTROGEN AND PROGESTERONE EXPRESSION LEVEL IN ENDOMETRIUM OF FEMALES UNDER TAMOXIFEN in the gland epithelium, 262.3±8.8 estrogen receptors in the stroma; 289.4±10.2 progesterone receptors

Molecular profile of salivary gland tumors: discovering new targets for therapy; [Молекулярно-генетический портрет рака слюнных желез: поиск новых мишеней для таргетной терапии] receptor (ER), progesterone receptor (pR), pan-TRk) and molecular genetic targets (ALK, BRAF, ERBB2, KIT

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