По вашему запросу найдено документов: 458

Страница 1 из 46

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)
for differentially expressed genes (DEGs) in ICH, with a fold change (FC) value of (|log2FC|) > 2 and a P-value of <0
CHEMOKINE GENE POLYMORPHISMS ASSOCIATION WITH INCREASED RISK OF TYPE 2 DIABETES MELLITUS IN TATAR ETHNIC GROUP, RUSSIA
KOCHETOVA, O.V., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
loci in CCL20 (rs6749704) and CCL5 (rs2107538) genes with type 2 diabetes had been identified as a
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)
established that, in Tatars, the rs37973 G allele of the GLCCI1 gene is a marker of an increased risk
IL1RN MEDIATES THE SUPPRESSIVE EFFECT OF METHIONINE DEPRIVATION ON GLIOMA PROLIFERATION
WANG, K., LIU, H., LIU, J., WANG, X., TENG, L., ZHANG, J., CHEN, X., WANG, N., ZHONG, Y., HOU, X., JIANG, H., ZHANG, X., ZHAO, S., LIU, Y., YAO, Y., WANG, J., QU, Y., PENG, F., BEYLERLI, O., LIAO, X. (2019)
confirmed that IL1RN is a tumor associated gene and its expression is negatively correlated
ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
KORYTINA, G.F., AKHMADISHINA, L.Z., KOCHETOVA, O.V., VIKTOROVA, T.V., AZNABAEVA, Y.G., ZAGIDULLIN, N.SH., ZAGIDULLIN, SH.Z., KZHYSHKOWSKA, J.G (2019)
Background and objective: Chronic obstructive pulmonary disease (COPD) is a complex chronic
COMPARISON OF PREDICTIVE IN SILICO TOOLS ON MISSENSE VARIANTS IN GJB2, GJB6, AND GJB3 GENES ASSOCIATED WITH AUTOSOMAL RECESSIVE DEAFNESS 1A (DFNB1A)
PSHENNIKOVA, V.G., BARASHKOV, N.A., ROMANOV, G.P., TERYUTIN, F.M., SOLOV'EV, A.V., GOTOVTSEV, N.N., NIKANOROVA, A.A., FEDOROVA, S.A., NAKHODKIN, S.S., SAZONOV, N.N., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L, DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2019)
predictions for missense variants of the GJB2 (Cx26), GJB6 (Cx30), and GJB3 (Cx31) connexin genes associated
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)
. We highlight the therapeutic potential of gene therapy as a novel and innovative approach for future
ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Korytina, G.F., Akhmadishina, L.Z., Aznabaeva, Y.G., Kochetova, O.V., Zagidullin, N.S., Kzhyshkowska, J.G., Zagidullin, S.Z., Viktorova, T.V. (2019)
Background and objective: Chronic obstructive pulmonary disease (COPD) is a complex chronic
THE ROLE OF THE IMMUNE RESPONSE MEDIATOR GENES POLYMORPHISM IN THE PREDISPOSITION TO JUVENILE IDIOPATHIC ARTHRITIS
NAZAROVA, L.S., DANILKO, K.V., MALIEVSKY, V.A., BAKIROV, A.B., VIKTOROVA, T.V. (2019)
Objective - The aim of the work was to study the contribution of the immune response mediator genes
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)
. Приблизительно 6% наследственного РЯ приходится на герминальные мутации в генах BARD1, BRIP1, CHEK, MRE11A, MSH6

Страница 1 из 46

Google Scholar
OpenDoar

Фасеты

Авторы
Ключевые слова
Год