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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
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
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)
gene, Taq1 and rs6275 of the DRD2 gene, rs6280 of the DRD3 gene, VNTR 120bp, VNTR 48bp and rs747302
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
ПОЛИМОРФНЫЕ ВАРИАНТЫ ГЕНОВ ГЛУТАМАТНЫХ (GRIK5, GRIN2B) И СЕРОТОНИНОВОГО (HTR2A) РЕЦЕПТОРОВ АССОЦИИРОВАНЫ С ХРОНИЧЕСКОЙ ОБСТРУКТИВНОЙ БОЛЕЗНЬЮ ЛЕГКИХ
POLYMORPHIC VARIANTS OF GLUTAMATE RECEPTOR (GRIK5, GRIN2B) AND SEROTONIN RECEPTOR (HTR2A) GENES ARE ASSOCIATED WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Korytina, G.F., Akhmadishina, L.Z., Kochetova, O.V., Aznabaeva, Y.G., Zagidullin, Sh.Z., Victorova, T.V., Корытина Г.Ф., Ахмадишина Л.З., Кочетова О.В., Азнабаева Ю.Г., Загидуллин Ш.З., Викторова Т.В. (2017)
), GRIN2B (rs2268132), and CHRNB4 (rs1948) gene polymorphisms and COPD, as well as the contribution
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

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