По вашему запросу найдено документов: 47

Страница 1 из 5

ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ СИНДРОМА ДЕФИЦИТА ВНИМАНИЯ/ГИПЕРАКТИВНОСТИ. СОВРЕМЕННОЕ СОСТОЯНИЕ ПРОБЛЕМЫ
GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS OF THE PROBLEM
Р. Р. Шарафиев, R. R. Sharafiev, А. Р. Асадуллин, A. R. Asadullin, В. Л. Юлдашев, V. L. Yuldashev, А. В. Анцыборов, A. V. Antsyborov, Л. В. Лямина, L. V. Lyamina, Э. А. Ахметова, E. A. Akhmetova (Медицинский вестник Башкортостана, №4, 2018)
THE IMMUNE RESPONSE MEDIATOR GENES POLYMORPHIC VARIANTS AS PREDICTORS OF THE ETANERCEPT EFFICACY IN JUVENILE IDIOPATHIC ARTHRITIS
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Bakirov, A.B., Viktorova, T.V. (2018)
Objective - The aim of the study was to investigate the relationship of the alleles and genotypes
Роль полиморфного локуса VNTR гена аггрекана в развитии остеоартроза у женщин
The role of VNTR aggrecan gene polymorphism in the development of osteoarthritis in women
Shapovalova, D.A., Tyurin, A.V., Litvinov, S.S., Kchusnutdinova, E.K., Khusainova, R.I., Д.А. Шаповалова, А.В.Тюрин, С.С. Литвинов, Э.К. Хуснутдинова, Р.И. Хусаинова (2018)
of the localization of the pathological process, as well as with the presence of uCTO signs. Twelve allelic variants
12-Month Effects of Once-Weekly and Twice-Monthly Administration of Hybrid Fc-Fused Human Growth Hormone, GX-H9, Treatment in Pediatric with GHD Deficiency
Malieyskiy, O., Mykola, A., Nataliya, Z., Bolshova, E.V., Senatorova, G., Oroszlan, G., Skorodok, J., Peterkova, V., Nataliya, C., Sorokman, T., Yang, S., Lee, J.E., Muzsnai, A., Hwang, J.S., Lee, S.Y., Choi, Y.J., Ji, H.J., Woo, J., Sung, Y.C. (2018)
GX-H9 is a long-acting form of recombinant human GH under clinical development for both adults
PSORIASIS PATIENTS DEMONSTRATE HLA-CW*06:02 ALLELE DOSAGE-DEPENDENT T CELL PROLIFERATION WHEN TREATED WITH HAIR FOLLICLE-DERIVED KERATIN 17 PROTEIN
Yunusbaeva, M., Valiev, R., Bilalov, F., Sultanova, Z., Sharipova, L., Yunusbayev, B. (2018)
that the HLA-Cw*06:02 allele dosage strongly predicted the T cell response. Our study findings suggest
РОЛЬ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНА Β2-АДРЕНЕРГИЧЕСКОГО РЕЦЕПТОРА (ADRB2) В РАЗВИТИИ И ТЕЧЕНИИ БРОНХИАЛЬНОЙ АСТМЫ
THE ROLE OF Β2-ADRENERGIC RECEPTOR GENE (ADRB2) POLYMORPHISMS IN ASTHMA
О. Н. Савельева, O. N. Savelieva, А. С. Карунас, A. S. Karunas, Ю. Ю. Федорова, Yu. Yu. Fedorova, Э. К. Хуснутдинова, E. K. Khusnutdinova (Медицинский вестник Башкортостана, №5, 2018)
CXCL13 POLYMORPHISM IS ASSOCIATED WITH ESSENTIAL HYPERTENSION IN TATARS FROM RUSSIA
TIMASHEVA, YA.R., NASIBULLIN, T.R., TUKTAROVA, I.A., ERDMAN, V.V., MUSTAFINA, O.E (2018)
strong association of CXCL13 rs355689*C allele with essential hypertension under additive (OR 0.56, PFDR
ASSOCIATIONS OF POLYMORPHIC DNA MARKERS AND THEIR COMBINATIONS WITH MULTIPLE SCLEROSIS
Zaplakhova, O. V., Nasibullin, T. R., Tuktarova, I. A., Timasheva, Y. R., Erdman, V. V., Bakhtiyarova, K. Z., Mustafina, O. E. (2018)
of alleles associated with increased risk of MS separately for women and men, in which the most frequent
Statistical and Intelligent Methods of Medical Data Processing
Shakhmametova, G.R., Yusupova, N.I., Mironov, V.V., Zulkarneev, R.K. (2018)
non-parametric methods
PECULIARITIES OF FORMATION OF CARCINOGENIC RISK UNDER THE INFLUENCE OF TECHNOLOGICAL EFFECTS OF PETROCHEMICAL TYPE
VASILYEVA, E.V., SITDIKOVA, I.D., KAMALETDINOVA, A.A., LOPUSHOV, D.V., USMANOVA, I.N., GERASIMOVA, L.I. (2018)
feedstocks, which entails the emittance of non-carcinogenic substance, namely ethylene and carcinogens

Страница 1 из 5

Фасеты

Авторы
Ключевые слова
Год
Google Scholar
OpenDoar