Zobrazeno 1 - 10
of 747
pro vyhledávání: '"A. P. Sokolenko"'
Autor:
A. P. Sokolenko, S. V. Poletaeva, A. D. Shestakova, T. V. Gorodnova, I. V. Berlev, E. N. Imyanitov
Publikováno v:
Сибирский онкологический журнал, Vol 23, Iss 2, Pp 139-146 (2024)
Background. Homologous recombination deficiency (HRD) is a valuable molecular marker for predicting response to platinum agents and poly(ADP-ribose)-polymerase (PARP) inhibitors. Germline and somatic alterations in the BRCA1 and BRCA2 genes are the m
Externí odkaz:
https://doaj.org/article/1bd86b06748f4449b57fdf1f2994415c
Autor:
Y. V. Belysheva, E. K. Bakaeva, A. R. Venina, A. A. Romanko, G. A. Raskin, A. P. Sokolenko, E. N. Suspitsin, A. A. Avetisyan, S. V. Orlov, E. N. Imyanitov
Publikováno v:
Сибирский онкологический журнал, Vol 22, Iss 6, Pp 83-91 (2024)
The aim of the study was to compare the spectra of pathogenic BRCA1 and BRCA2 variants in patients with hereditary breast cancer (BC) and ovarian cancer (OC) from two groups of ethnic Armenians: Yerevan and cities of southern Russia.Material and Meth
Externí odkaz:
https://doaj.org/article/fba47bd88bee4bc68054576336395c77
Autor:
D. A. Enaldieva, P. V. Krivorotko, E. N. Imyanitov, E. K. Zhiltsova, R. V. Donskikh, A. P. Sokolenko, L. F. Shaykhelislamova, T. T. Tabagua, L. P. Gigolaeva, A. V. Komyakhov, K. S. Nikolaev, K. Yu. Zernov, S. S. Ereshchenko, R. M. Paltuev, A. A. Bessonov, A. S. Artemyeva, R. S. Pesotskiy, N. S. Amirov, A. S. Emelyanov, V. V. Mortada, Ya. I. Bondarchuk, V. V. Semiglazov, T. Yu. Semiglazova, V. F. Semiglazov, A. M. Belyaev
Publikováno v:
Опухоли женской репродуктивной системы, Vol 19, Iss 1, Pp 48-55 (2023)
Background. BRCA-associated triple negative breast cancer (TNBC) is considered one of the most aggressive subtypes of breast cancer with high sensitivity to chemotherapy, which leads to increased interest in finding new treatment options for patients
Externí odkaz:
https://doaj.org/article/f7969acdde894223bd4331d72b66866d
Publikováno v:
Сибирский онкологический журнал, Vol 21, Iss 5, Pp 123-134 (2022)
Background. Hereditary genetic mutations are a significant risk factor for malignant transformation of cells and cancer development. Hereditary genetic mutations account for 15 to 25 % of all ovarian carcinomas. Purpose of the study: to summarize dat
Externí odkaz:
https://doaj.org/article/d3954e4825e14a9bb93d9b5fdb3c4b21
Pulsars convert a significant fraction of their total spin-down power into very high-energy electrons, leading to the formation of TeV halos. It is not yet known, however, whether these sources also efficiently accelerate electrons at lower energies
Externí odkaz:
http://arxiv.org/abs/2405.06739
Autor:
Aramburo-Garcia, Andres, Bondarenko, Kyrylo, Boyarsky, Alexey, Kashko, Pavlo, Pradler, Josef, Sokolenko, Anastasia, Kugel, Roi, Schaller, Matthieu, Schaye, Joop
The resonant conversion, within the inter-galactic medium, of regular photons into dark photons amplifies the anisotropy observed in the CMB, thereby imposing stringent constraints on the existence of light dark photons. In this study, we investigate
Externí odkaz:
http://arxiv.org/abs/2405.05104
We use Faraday rotation measurements from the latest catalog LoTSS DR2 from LOFAR to probe intergalactic magnetic fields. To identify the extragalactic component of the observed rotation measure (RM) we use two different techniques: residual rotation
Externí odkaz:
http://arxiv.org/abs/2404.17402
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 25, Iss 2, Pp 7-18 (2018)
Hereditary breast and ovarian cancer is one of the most common genetic pathology. Medical and genetic counseling of patients with hereditary breast and ovarian cancer and their families plays the important role in cancer care, as it helps to develop
Externí odkaz:
https://doaj.org/article/445fa1669c4449ecb2bec7f557f6851f
Autor:
A. О. Ivantsov, M. A. Kleshchov, Т. V. Gorodnova, A. P. Sokolenko, Kh. B. Kotiv, I. D. Amelina, А. Е. Mikhnin, А. F. Urmancheeva, I. V. Berlev, Е. N. Imyanitov
Publikováno v:
Сибирский онкологический журнал, Vol 17, Iss 1, Pp 99-103 (2018)
Inherited mutations in the BRCA1 and BRCA2 genes more often provoke the development of metachronous tumors compared to the general population. Women who carry inherited BRCA1 mutations have an increased risk of developing not only breast and ovarian
Externí odkaz:
https://doaj.org/article/9ed5c2294d494a9fbde276396fd8e83b
Autor:
K. B. Kotiv, T. V. Gorodnova, A. O. Ivantsov, A. G. Iyevleva, S. N. Aleksakhina, G. M. Manichas, A. S. Lisyanskaya, R. P. Salomatov, M. S. Shushaniia, M. V. Borodenko, L. D. Roman, G. I. Mikhailiuk, O. N. Mikheeva, T. G. Grigorieva, I. V. Berlev, E. N. Imyanitov, A. P. Sokolenko
Publikováno v:
Сибирский онкологический журнал, Vol 16, Iss 6, Pp 31-40 (2017)
Germ-line mutations in BRCA1 and BRCA2 genes are the most established risk factors for hereditary breast and ovarian cancers. The purpose of the study was to analyze BRCA1/2 testing in ovarian cancer patients. Materials and methods. We analyzed 222 p
Externí odkaz:
https://doaj.org/article/31f595ac4f1a4d64a72ee96e73f7dd63