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THE ROLE OF REVERSE TRANSCRIPTASE IN THE ORIGIN OF LIFE
MUSTAFIN, R.N., KHUSNUTDINOVA, E.K. (2019)
potential for the transformation into protein-coding genes. Hence, the conserved principles of RNA, DNA
СТРЕСС-ИНДУЦИРОВАННАЯ АКТИВАЦИЯ ТРАНСПОЗОНОВ В ЭКОЛОГИЧЕСКОМ МОРФОГЕНЕЗЕ
THE ROLE OF TRANSPOSABLE ELEMENTS IN THE ECOLOGICAL MORPHOGENESIS UNDER THE INFLUENCE OF STRESS
МУСТАФИН, Р.Н., ХУСНУТДИНОВА, Э.К., Mustafin R.N., Khusnutdinova E.K. (2019)
ВЗАИМОСВЯЗЬ ТРАНСПОЗОНОВ С ТЕЛОМЕРАМИ ПРИ СТАРЕНИИ
AGING AND INTERRELATION OF TELOMERES WITH TRANSPOSABLE ELEMENTS
МУСТАФИН, Р.Н., Mustafin R.N. (2019)
NON-CODING RNA
IDENTIFICATION OF HUB GENES AND SMALL-MOLECULE COMPOUNDS RELATED TO INTRACEREBRAL HEMORRHAGE WITH BIOINFORMATICS ANALYSIS
LIU, Z., ZHANG, R., CHEN, X., YAO, P., YAN, T., LIU, W., YAO, J., ZHAO, S., SOKHATSKII, A., GAREEV, I. (2019)
of intracerebral hemorrhage (ICH). We aimed to identify the hub genes associated with intracerebral hemorrhage
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
FEDOROVA, Y.Y., KARUNAS, A.S., GIMALOVA, G.F., KHUSNUTDINOVA, E.K., SAVELIEVA, O.N, MURZINA, R.R., GATIYATULLIN, R.F., ETKINA, E.I. (2019)
-box and leucine-rich repeat protein gene (FBXL7), rs11123610 of the allantoicase gene (ALLC). It has been
ПОИСК МУТАЦИЙ В ГЕНЕ ИНТЕРФЕРОН-ИНДУЦИРОВАННОГО ТРАНСМЕМБРАННОГО БЕЛКА 5 (IFITM5) У БОЛЬНЫХ НЕСОВЕРШЕННЫМ ОСТЕОГЕНЕЗОМ
SEARCH FOR MUTATIONS OF THE INTERFERON-INDUCED TRANSMEMBRANE PROTEIN 5 (IFITM5) GENE IN PATIENTS WITH OSTEOGENESIS IMPERFECTA
Зарипова, А.Р., Нургалиева, Л.Р., Тюрин, А.В., Минниахметов, И.Р., Хусаинова, Р.И., Zaripova, A.R., Nurgalieva, L.R., Tyurin, A.V., Minniakhmetov, I.R., Khusainova, R.I. (2019)
. Мутации в гене IFITM5, также назы ваемом BRIL (bone-restricted IFITM-like protein), участвующем в
PATHOPHYSIOLOGY OF CALCIUM MEDIATED VENTRICULAR ARRHYTHMIAS AND NOVEL THERAPEUTIC OPTIONS WITH FOCUS ON GENE THERAPY
Paar, V., Jirak, P., Larbig, R., Zagidullin, N.S., Brandt, M.C., Lichtenauer, M., Hoppe, U.C., Motloch, L.J. (2019)
in action potential generation and cardiac contraction, Ca2+ channels and Ca2+ handling proteins represent
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)
variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk
THE ROLE OF SERUM AMYLOID A1, ADHESION MOLECULES, CHEMOKINES, AND CHEMOKINE RECEPTORS GENES IN CHRONIC OBSTRUCTIVE PULMONARY DISEASE
KORYTINA, G.F., AKHMADISHINA, L.Z., KOCHETOVA, O.V., VIKTOROVA, T.V., AZNABAEVA, Y.G., ZAGIDULLIN, SH.Z. (2019)
was to investigate the association of COPD with alleles and genotypes of the genes that encode chemokines
НАСЛЕДСТВЕННЫЙ РАК ЯИЧНИКОВ: ВКЛАД ИЗМЕНЕНИЙ ГЕНОВ-КАНДИДАТОВ В ПАТОГЕНЕЗ ЗАБОЛЕВАНИЯ
THE HEREDITARY OVARIAN CANCER: ROLE OF CANDIDATE GENES IN DISEASE PATHOGENESIS
Фаисханова, Р.Р., Прокофьева, Д.С., Хуснутдинова, Э.К., Сакаева, Д.Д., Гордиев, М.Г., Faiskhanova, R.R., Prokofieva, D.S., Khusnutdinova, E.K., Sakaeva, D.D., Gordiev, M.G. (2019)
THE HEREDITARY OVARIAN CANCER: ROLE OF CANDIDATE GENES IN DISEASE PATHOGENESIS

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