Search Results - A. Yu. Molokov

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  1. 1

    Endogenous and exogenous risk factors affecting the incidence of breast cancer in the population of Yakutia by D. G. Tikhonov, A. Yu. Molokov, V. A. Belyavskaya, O. A. Ananina, P. A. Gervas

    Published 2023-06-01

    The purpose of the study: to analyze the breast cancer incidence and breast cancer risk factors for the population of the Republic of Sakha (Yakutia) in 2011-2020. Material and Methods. The incidence of breast cancer in the population of Yakutia was analyzed using the data collected from population-...

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  2. 2

    Ethnic aspects of hereditary breast cancer by P. A. Gervas, A. Yu. Molokov, E. V. Panpherova, L. Ph. Pisareva, N. V. Cherdyntseva

    Published 2019-04-01

    This study aimed to reveal the spectrum of BRca1 and BRca2 genes mutation in various ethnic groups of the Russian Federation. asystematic literature search includes data for the past 10 years and was conducted by using electronic databases of pubmed, eliBRaRY and ect.Material and methods. The review...

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  3. 3

    Variability of the mitochondrial genome in young Yakut patients with breast cancer by D. G. Tikhonov, A. N. Egorov, M. V. Golubenko, A. Yu. Molokov, V. A. Belyavskaya, P. A. Gervas, N. A. Skryabin

    Published 2024-01-01

    Background. The Sakha (Yakutia) population, the indigenous population of Siberia living in Yakutia, has one of the lowest rates of breast cancer (BC) incidence worldwide. The low BC incidence among the indigenous population of Yakutia has been reported by several authors, but to date the reasons for...

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  4. 4

    Whole exome sequencing: the search for mutations associated with hereditary breast cancer in ethnic groups of Siberia by P. A. Gervas, A. Yu. Molokov, N. N. Babyshkina, F. G. Ivanova, T. I. Nikolaeva, D. G. Tikhonov, E. L. Choynzonov, N. V. Cherdyntseva

    Published 2024-11-01

    Hereditary breast cancer (HBC) is a heterogeneous disease caused by mutations in genes characterized by ethnic specifcity. The clinical heterogeneity of this disease signifcantly complicates its diagnosis. The use of high-throughput sequencing is one of the approaches that allow the search for genes...

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  5. 5

    New mutation of the TP53 gene associated with the hereditary breast cancer in a young Tuvinian woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ponomareva, N. N. Babyshkina, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

    Published 2022-01-01

    Background. The identification of the ethnospecific mutations associated with hereditary breast cancer remains challenging. Next generation sequencing (Ngs) technology fully enables the compilation of germline variants associated with the risk for inherited diseases. Despite the success of the Ngs,...

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  6. 6

    A novel germline mutation of the <i>PALB2</i> gene in a young Yakut breast cancer woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ivanova, D. G. Tikhonov, N. S. Kipriyanova, A. N. Egorov, L. D. Zhuikova, N. A. Shefer, E. B. Topolnitskiy, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

    Published 2022-09-01

    Background. Breast cancer (BC) is the most common female malignancy worldwide. Partner And Localizer of BRCA2 gene (PALB2) is directly involved in DNA damage response. Germline mutation in PALB2 has been identified in breast cancer and familial pancreatic cancer cases, accounting for approximately 1...

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