Zobrazeno 1 - 10
of 21
pro vyhledávání: '"G N Khabas"'
Publikováno v:
Гинекология, Vol 20, Iss 6, Pp 42-47 (2018)
The aim of the work is to conduct a systematic analysis of the available research results on the possibility of using menopausal hormone therapy (MHT) in patients who successfully completed the treatment of endometrial cancer (EC). Materials and meth
Externí odkaz:
https://doaj.org/article/3053025164c847e3a40bf160b111be04
Autor:
D. L. Ovodenko, G. N. Khabas, Yu. M. Kreinina, A. A. Seregin, O. I. Aleshikova, L. A. Ashrafyan
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 3, Pp 82-89 (2021)
The aim of the study was to evaluate the five-year survival rate in patients with stage ib2–iiib cervical cancer treated with neoadjuvant chemotherapy and radical surgery.Material and Methods. Long-term treatment outcomes were studied in 173 patien
Externí odkaz:
https://doaj.org/article/72ad94385326433bb687bd83141cb368
Autor:
M. V. Iurova, V. V. Chagovets, S. V. Pavlovich, N. L. Starodubtseva, G. N. Khabas, K. S. Chingin, A. O. Tokareva, G. T. Sukhikh, V. E. Frankevich
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Epithelial ovarian cancer (OC) ranks first in the number of deaths among diseases of the female reproductive organs. Identification of OC at early stages is highly beneficial for the treatment but is highly challenging due to the asymptomatic or low-
Externí odkaz:
https://doaj.org/article/bf188c16397042a1b87ca3fd2eebafa4
Publikováno v:
Акушерство, гинекология и репродукция, Vol 13, Iss 4, Pp 369-383 (2020)
Introduction. Most pelvic tumors originate from reproductive organs. Even using the up-to-date imaging techniques, radiologists experience difficulties in determining the source of the lesion since a wide range of tumors look similar to each other on
Externí odkaz:
https://doaj.org/article/47750c44f27143fc98854df35abe9228
Autor:
P. K. Brenner, M. A. Kapralova, D. S. Khodyrev, S. V. Khokhlova, G. N. Khabas, A. V. Asaturova, Yu. V. Nosova, L. N. Kayumova, T. M. Zavarykina
Publikováno v:
Russian Journal of Genetics. 58:1154-1158
Autor:
T M Zavarikina, M B Stenina, P K Brenner, G N Khabas, D S Khodirev, Yu V Nosova, A S Tyulyandina, S V Khokhlova, M A Kapralova, A V Asaturova
Publikováno v:
Bulletin of Experimental Biology and Medicine. 171:755-759
We analyzed associations of polymorphic markers of DNA repair genes (XRCC1, ERCC2), cell cycle control genes (TP53, MDM2, and CDKN1A), methylation of promoter region, and mutation 5382insC of BRCA1 gene in ovarian cancer with effectiveness of platinu
Autor:
Anna Kolodkina, I B Kostrova, Z.K. Batyrova, G N Khabas, Natalia Yu. Kalinchenko, Z Kh Kumykova, A V Asaturova, E N Uvarova, Anatoly Tiulpakov
Publikováno v:
Problems of Endocrinology. 67:73-77
Mutations in the gene DHH are an extremely rare cause of disorders of sex development 46,XY (DSD,46XY). The article describes the clinical cases of two unrelated patients with gonadal dysgenesis 46,XY with female phenotype. By using a next generation
Autor:
Vitaly I. Loginov, M B Stenina, Yu A Nosova, M A Kapralova, G T Sukhikh, S V Khokhlova, A S Tyulyandina, P K Brenner, T. M. Zavarykina, A M Burdennyi, D. S. Khodyrev, G N Khabas, A V Asaturova, M. V. Atkarskaya
Publikováno v:
Bulletin of Experimental Biology and Medicine. 169:486-490
We studied the association of polymorphic markers of cell cycle control genes (Arg72Pro of the TP53 gene, T(-410)G of the MDM2 gene, and Ser31Arg of the CDKN1A gene) in ovarian cancer and progression-free survival following platinum-based chemotherap
Publikováno v:
Акушерство, гинекология и репродукция, Vol 13, Iss 4, Pp 369-383 (2020)
Introduction. Most pelvic tumors originate from reproductive organs. Even using the up-to-date imaging techniques, radiologists experience difficulties in determining the source of the lesion since a wide range of tumors look similar to each other on
Autor:
N Y, Kalinchenko, Z K, Batyrova, I B, Kostrova, A A, Kolodkina, E N, Uvarova, Z Kh, Kumykova, A V, Asaturova, G N, Khabas, A N, Tiulpakov
Publikováno v:
Problemy endokrinologii. 67(3)
Mutations in the gene DHH are an extremely rare cause of disorders of sex development 46,XY (DSD,46XY). The article describes the clinical cases of two unrelated patients with gonadal dysgenesis 46,XY with female phenotype. By using a next generation