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По вашему запросу найдено документов: 462

Страница 29 из 47

LYNCH SYNDROME GERMLINE MUTATIONS IN BREAST CANCER: NEXT GENERATION SEQUENCING CASE-CONTROL STUDY OF 1,263 PARTICIPANTS

NIKITIN, A.G., CHUDAKOVA, D.A., ENIKEEV, R.F., GORDIEV, M.G., SAKAEVA, D., DRUZHKOV, M., SHIGAPOVA, L.H., BROVKINA, O.I., SHAGIMARDANOVA, E.I., GUSEV, O.A. (2020)

LS-mutations into genetic counseling tests for patients with hereditary BC.

СОВРЕМЕННЫЕ МЕТОДЫ СОХРАНЕНИЯ ФЕРТИЛЬНОСТИ У ЖЕНЩИН С ОНКОЛОГИЧЕСКИМИ ЗАБОЛЕВАНИЯМИ

CURRENT FERTILITY PRESERVATION METHODS IN WOMEN WITH CANCER

Э. А. Фазлыева, E. A. Fazlyeva, М. П. Миронова, M. P. Mironova, Г. Г. Фасхутдинова, G. G. Faskhutdinova, Д. В. Исламгулов, D. V. Islamgulov (Креативная хирургия и онкология, №3, 2017)

MOLECULAR AND BIOCHEMICAL STUDY OF GLUTARIC ACIDURIA TYPE 1 IN 49 RUSSIAN FAMILIES: NINE NOVEL MUTATIONS IN THE GCDH GENE

KURKINA, M.V., MIHAYLOVA, S.V., BAIDAKOVA, G.V., SAIFULLINA, E.V., KOROSTELEV, S.A., PYANKOV, D.V., KANIVETS, I.V., YUNIN, M.A., PECHATNIKOVA, N.L., ZAKHAROVA, E.YU (2020)

genetic characteristics of 51 patients diagnosed with GA1 from 49 unrelated families in Russia. We

THE FANCM:P.ARG658* TRUNCATING VARIANT IS ASSOCIATED WITH RISK OF TRIPLE-NEGATIVE BREAST CANCER

Bogliolo, M., Catucci, I., Caleca, L., Lasheras, S.V., Pujol, R., Kiiski, J.I., Muranen, T.A., Barnes, D.R., Dennis, J., Michailidou, K., Bolla, M.K., Leslie, G., Figlioli, G. (2019)

Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic

DOES ESCHERICHIA COLI HAVE PATHOGENIC POTENTIAL AT A LOW LEVEL OF BACTERIURIA IN RECURRENT, UNCOMPLICATED URINARY TRACT INFECTION?

NABOKA, Y.L., MAVZYUTOV, A.R., KOGAN, M.I., GUDIMA, I.A., IVANOV, S.N., NABER, K.G. (2020)

colony-forming units (CFU)/mL is not usually investigated. Objective: To determine the molecular-genetic

Origin and diffusion of human Y chromosome haplogroup J1-M267

frequency, nevertheless demonstrates high genetic diversity. Studies associate this haplogroup

Опыт применения вспомогательных репродуктивных технологий в Республике Башкортостан

Experience of using assisted reproductive technologies in the republic of Bashkortostan

Sugurova, A.T., Minniakhmetov, I.R., Zabelin, M.V., Yashchuk, A.G., Khusainova, R.I., СУГУРОВА, А.Т., МИННИАХМЕТОВ, И.Р., ЗАБЕЛИН, М.В., ЯЩУК, А.Г., ХУСАИНОВА, Р.И. (2021)

the quality and viability of embryos, widespread introduction of preimplantation genetic testing to exclude

The association study of polymorphic variants of hypothalamic-pituitary-adrenal system genes (AVPR1B, OXTR) and aggressive behavior manifestation: A focus on social environment

Kazantseva, A.V., Davydova, Y.D., Enikeeva, R.F., Valinurov, R.G., Gareeva, A.E., Khusnutdinova, N.N., Khusnutdinova, E.K. (2021)

study is aimed to estimate both the genetic- and haplotype-based effects of the OXTR and AVPR1B genes

PREDICTING THE RISK OF DEVELOPING VIBRATION DISEASE AND VEGETATIVE-SENSORY POLYNEUROPATHY UNDER VIBRATION EXPOSURE USING ANALYSIS OF CANDIDATE GENE POLYMORPHISM

Mukhammadiyeva, G.F., Shaikhlislamova, E.R., Karimov, D.D., Karimov, D.O., Repina, E.F., Yakupova, T.G., Kudoyarov, E.R. (2024)

and TNF-α genes can be considered probable molecular genetic predictors of VD and ASPN. © (2024), (Federal

MicroRNA Expression Signatures in Clear Cell Renal Cell Carcinoma: High-Throughput Searching for Key miRNA Markers in Patients from the Volga-Ural Region of Eurasian Continent

Gilyazova, Irina, Ivanova, Elizaveta, Izmailov, Adel, Sharifgaliev, Ildar, Karunas, Alexandra, Pudova, Elena, Kobelyatskaya, Anastasiya, Gilyazova, Gulshat, Izmailova, Angelina, Pavlov, Valentin, Khusnutdinova, Elza (2023)

Clear cell renal cell carcinoma (ccRCC) is characterized by high molecular genetic heterogeneity

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