По вашему запросу найдено документов: 454

Страница 1 из 46

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)
of the DRD4 gene (dopamine receptors), (TCAT)n-repeats of the TH gene (tyrosine hydroxylase), rs4680
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
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
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
OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS
Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)
children with HI due to mutations in the GJB2 gene and 91 questionnaires about the presumed causes
ВЗАИМОСВЯЗЬ ЭНДОТЕЛИАЛЬНОЙ ДИСФУНКЦИИ С ПОЛИМОРФИЗМОМ ГЕНОВ SELP И VEGF У ЖЕНЩИН С МЕТАБОЛИЧЕСКИМ СИНДРОМОМ И АРТЕРИАЛЬНОЙ ГИПЕРТОНИЕЙ
INTERDEPENDENCE OF ENDOTHELIAL DYSFUNCTION WITH POLYMORPHISM OF SELP AND VEGF GENES IN WOMEN WITH METABOLIC SYNDROME AND ARTERIAL HYPERTENSION
З. М. Исламгалеева, Z. M. Islamgaleeva, Л. Н. Мингазетдинова, L. N. Mingazetdinova, А. В. Кабилова, A. V. Kabilova, А. Б. Бакиров, A. B. Bakirov (Медицинский вестник Башкортостана, №6, 2017)
INTERDEPENDENCE OF ENDOTHELIAL DYSFUNCTION WITH POLYMORPHISM OF SELP AND VEGF GENES IN WOMEN
ГЕНОТИПИЧЕСКИЕ ОСОБЕННОСТИ БОЛЬНЫХ ГНЕЗДНОЙ АЛОПЕЦИЕЙ В УСЛОВИЯХ ВОЗДЕЙСТВИЯ ХИМИЧЕСКИХ СРЕДОВЫХ ФАКТОРОВ
GENOTYPIC CHARACTERISTICS OF PATIENTS WITH ALOPECIA AREATA UNDER EXPOSURE TO CHEMICAL ENVIRONMENTAL FACTORS
Н. П. Сетко, N. P. Setko, Т. В. Николаева, T. V. Nikolaeva, Л. Г. Воронина, L. G. Voronina (Медицинский вестник Башкортостана, №1, 2017)
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

Страница 1 из 46

Google Scholar
OpenDoar

Фасеты

Авторы
Ключевые слова
Год