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РОЛЬ МЕЖГЕННЫХ ВЗАИМОДЕЙСТВИЙ ГЕНОВ НЕЙРОТРОФИЧЕСКОЙ И НЕЙРОМЕДИАТОРНОЙ СИСТЕМЫ В РАЗВИТИИ ПРЕДРАСПОЛОЖЕННОСТИ К ПАРАНОИДНОЙ ШИЗОФРЕНИИ
THE ROLE OF INTERGENIC INTERACTIONS OF NEUROTROPHIC AND NEUROTRANSMITTER SYSTEM GENES IN THE DEVELOPMENT OF SUSCEPTIBILITY TO PARANOID SCHIZOPHRENIA
GAREEVA, A.E., KHUSNUTDINOVA, E.K., ГАРЕЕВА А.Э., ХУСНУТДИНОВА Э. (2020)
of six genes of the neurotrophin and neurexin system (BDNF, NTRK2, NTRK3, NGF, NXPH1, NRXN1) and nine
THE ASSOCIATION BETWEEN EATING BEHAVIOR AND POLYMORPHISMS IN GRIN2B, GRIK3, GRIA1 AND GRIN1 GENES IN PEOPLE WITH TYPE 2 DIABETES MELLITUS
KOCHETOVA, O.V., KORYTINA, G.F., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2020)
genes (GRIN2B, GRIK3, GRIA1, GRIN1). Three SNPs were associated with type 2 diabetes: rs7301328 in GRIN2
POLYMORPHISM OF FOLATE CYCLE GENES AS A RISK FACTOR OF HYPERHOMOCYSTEINEMIA
Ivanov, A.M., Gil'manov, A.Z., Malyutina, N.N., Khovaeva, Y.B., Nenasheva, O.Y., El'kin, G.I., Sosnin, D.Y. (2020)
in blood serum for the remaining 4 SNP in folate cycle genes (р> 0.1). Examined SNP in MTHFR and MTR genes
АНАЛИЗ АССОЦИАЦИЙ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ АМИНОКСИДАЗЫ 1 AOC1 И ГИСТАМИН-N-МЕТИЛТРАНСФЕРАЗЫ HNMT С РАЗВИТИЕМ БРОНХИАЛЬНОЙ АСТМЫ У ДЕТЕЙ
Association analysis of amine oxidase 1 AOC1 and histamine-N-methyl-transferase HNMT genes polymorphism with the development of asthma in children
Savelyeva, O.N., Karunas, A.S., Fedorov, Y.Y., Gatiyatullin, R.F., Etkina, E.I., Khusnutdinova, E.K., Савельева, О.Н., Карунас, А.С., Федорова, Ю.Ю., Гатиятуллин, Р.Ф., Эткина, Э.И., Хуснутдинова, Э.К. (2020)
* CC genotype and the rs1049793 * C allele of the AOC1 gene with the development of.. were revealed
FINE-MAPPING OF 150 BREAST CANCER RISK REGIONS IDENTIFIES 191 LIKELY TARGET GENES
FACHAL, L., KAR, S., TYRER, J.P., GHOUSSAINI, M., HARRINGTON, P.A., HEALEY, C.S., MAYES, R., SHAH, M., PHAROAH, P.D.P., EASTON, D.F., DUNNING, A.M., ASCHARD, H., JIANG, X., TAMIMI, R.M., KHUSNUTDINOVA, E., BIAŁKOWSKA, K., и др. соавторы (2020)
significantly over-represented in active gene regulatory regions and transcription factor binding sites. We
The Study of Association of Polymorphic Markers of the SOD1, SOD2, and SOD3 Genes with Longevity
Erdman, V.V., Nasibullin, T.R., Tuktarova, I.A., Timasheva, Y.R., Danilko, K.V., Viktorova, T.V., Mustafina, O.E. (2020)
the polymorphic markers in the genes of the antioxidant defense enzymes—SOD1 (rs2070424), SOD2 (rs4880), and SOD3
INVESTIGATION OF THE ROLE OF MICRORNA ASSOCIATED WITH THE VHL-HIFα-DEPENDENT PATHWAY IN PATIENTS WITH CLEAR CELL RENAL CELL CARCINOMA
KLIMENTOVA, E.A., GILYAZOVA, I.R., BERMISHEVA, M.A., BLINNIKOVA, A. M., SAFIULLIN, R.I., IZMAILOV, A.A., YANG, B., PAVLOV ., V.N, KHUSNUTDINOVA, E.K. (2020)
are accompanied by inactivation of the von Hippel–Lindau gene (VHL). It is known that VHL is a target for several
ИССЛЕДОВАНИЕ РОЛИ ПОЛИМОРФНОГО ВАРИАНТА ГЕНА АМИНОКСИДАЗЫ 1 (AOC1) В РАЗВИТИИ И ТЕЧЕНИИ БРОНХИАЛЬНОЙ АСТМЫ
THE ROLE OF AMINOXIDASE 1 (AOC1) GENE POLYMORPHISM IN THE DEVELOPMENT AND COURSE OF ASTHMA
Федорова, Ю.Ю., Савельева, О.Н., Карунас, А.С., Мурзина, Р.Р., Актаева, Е.Е., Гатиятуллин, Р.Ф., Эткина, Э.И., Хуснутдинова, Э.К., Yu.Yu. Fedorova, O.N. Savelieva, A.S. Karunas, R.R. Murzina, E.E. Aktaeva, R.F. Gatijatullin, E.I. Еtkina, E.K. Khusnutdinova (2020)
аминоксидазы 1 AOC1 с развитием и течением БА у детей. Материалом для исследования послужили образцы ДНК 637
The involvement of hypothalamic-pituitary-adrenal and monoaminergic systems genes in developing aggressive behaviour
DAVYDOVA, Y., KAZANTSEVA, A., ENIKEEVA, R., MUSTAFIN, R., MALYKH, S., LOBASKOVA, M., VALINUROV, R., AKHMEROVA, I., KHUSNUTDINOVA, E. (2020)
hereditary, but specific gene-environmental (G ×E) mechanisms mediating the genetic risk for aggres- sion
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)
detected in two patients. Genes located in the area of imbalance were KLF1, DNASE2, and GCDH. Patients

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