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THE ASSOCIATION OF THE PTPN22 RS2476601 GENE POLYMORPHISM WITH JUVENILE IDIOPATHIC ARTHRITIS IN CHILDREN FROM RUSSIA
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2017)
factors [1]. The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene single
INVESTIGATION OF THE ROLE OF CYTOKINE GENES POLYMORPHISMS IN THE DEVELOPMENT OF THE URTICARIA IN THE REPUBLIC OF BASHKORTOSTAN
Gimalova, G.K., Karunas, A.S., Khusuntdinova, E.K., Khantimerova, E.F., Zagidullin, S.Z. (2017)
of interleukins genes IL4 (rs2243250), IL4R (rs1805010), IL10 (rs1800872), IL13 (rs20541) and tumor necrosis
MATERIALS OF THE SCIENTIFIC-PRACTICAL CONFERENCE WITH INTERNATIONAL PARTICIPATION "MODERN APPROACHES AND PROSPECTS OF GENETIC RESEARCH IN YAKUTIA", SEPTEMBER 7, 2017, YAKUTSK
Akhmadeeva, G.N., Khidiyatova, I.M., Nasibullin, T.R., Baitimerov, A.R., Magzhanov, R.V., Khusnutdinova, F.K. (2017)
). We analyzed the polymorphic variants of the genes of the dopaminergic system: the rs4532 of the DRD1
RECONSTRUCTION OF SNP HAPLOTYPES WITH MUTATION C.-23+1G>A IN HUMAN GENE GJB2 (CHROMOSOME 13) IN SOME POPULATIONS OF EURASIA
Solovyev, A.V., Barashkov, N.A., Bady-Khoo, M.S., Zytsar, M.V., Posukh, O.L., Romanov, G.P., Rafailov, A.M., Sazonov, N.N., Alexeev, A.N., Dzhemileva, L.U., Khusnutdinova, E.K., Fedorova, S.A. (2017)
The c.-23+1G>A splice site mutation is one of the most frequent mutations of gene GJB2 (Cx26, 13q11
HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA
Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A. (2017)
carrier frequency of c.35delG, c.167delT and c.235delC mutations of the GJB2 gene in 17 populations
ГЕНЕТИЧЕСКИЕ МАРКЕРЫ ОСТЕОАРТРИТА У ЖЕНЩИН С НЕДИФФЕРЕНЦИРОВАННОЙ ДИСПЛАЗИЕЙ СОЕДИНИТЕЛЬНОЙ ТКАНИ
SEARCH FOR OSTEOARTHRITIS GENETIC MARKERS IN WOMEN WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA
Khusainova, R.I., Tyurin, A.V., Shapovalova, D.A., Khusnutdinova, E.K., Хусаинова Р.И., Тюрин А.В., Шаповалова Д.А., Хуснутдинова Э.К. (2017)
We conducted an association study of ten polymorphisms in six candidate genes of OA (rs1799750 (MMP
CLINICAL AND EPIDEMIOLOGICAL CHARACTERISTICS OF HEREDITARY MOTOR-SENSORY NEUROPATHY 1X CAUSED BY THE MUTATION C. 259C> G (P. P87A) IN THE GJB1 GENE OF PATIENTS FROM THE REPUBLIC OF BASHKORTOSTAN
Saifullina, E.V., Magzhanov, R.V., Khidiyatova, I.M., Khusnutdinova, E.K. (2017)
-sensory neuropathies caused by mutations in the GJB1 gene (gap junction B1 type). The authors have established earlier
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ ИССЛЕДОВАНИЯ ФУНКЦИОНИРОВАНИЯ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ ЦИТОКИНОВОЙ СЕТИ И БИОТРАНСФОРМАЦИИ КСЕНОБИОТИКОВ ПРИ ОНКОПАТОЛОГИИ
MOLECULAR GENETICS STUDY FUNCTIONING POLYMORPHIC GENE VARIANTS CYTOKINE NETWORK AND BIOTRANSFORMATION OF XENOBIOTICS FOR CANCER
Е. В. Воробьева, E. V. Vorobyeva, Э. М. Васильева, E. M. Vasilyeva, Г. Ф. Галикеева, G F. Galikeeva, В. Ю. Горбунова, V. Y. Gorbunova (Креативная хирургия и онкология, №4, 2017)
MOLECULAR GENETICS STUDY FUNCTIONING POLYMORPHIC GENE VARIANTS CYTOKINE NETWORK
ВЗАИМОСВЯЗЬ ПОЛИМОРФИЗМА ГЕНА ФАКТОРА НЕКРОЗА ОПУХОЛИ АЛЬФА С РАЗВИТИЕМ ГНОЙНО-СЕПТИЧЕСКИХ ОСЛОЖНЕНИЙ ТЯЖЕЛОГО ОСТРОГО ПАНКРЕАТИТА
Lutfarakhmanov, I.I. / Лутфарахманов И.И., Mironov, P.I. / Миронов П.И., Tikhonov, A.S. / Тихонов А.С. (2017)
The aim of study was to evaluate the relationship of tumor necrosis factor alpha gene polymorphism
GENETIC ASPECTS OF KERATOCONUS DEVELOPMENT
Bikbova, M.M., Usubova, E.L., Oganisyana, K.Kh., Lobov, S.L., Khasanovad, R.R., Dzhemilevab, L.U., Khusnutdinova, E.K. (2017)
development is widely recognized. To date, a large number of candidate genes have been investigated

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