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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
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)
revealed that some SNPs in chemokine genes are associated with obesity, insulin resistance, type 2 diabetes
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
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)
polymorphic variants of four genes involved in the metabolism of glucocorticosteroids in patients with asthma
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)
parenchyma. This work was designed as a case-control study aimed at investigating the association of the NRF2
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)
and processes responsible for arrhythmogenesis remains incomplete. Given the crucial role of Ca2+-handling
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., Aznabaeva, Y.G., Kochetova, O.V., Zagidullin, N.S., Kzhyshkowska, J.G., Zagidullin, S.Z., Viktorova, T.V. (2019)
parenchyma. This work was designed as a case-control study aimed at investigating the association of the NRF2
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
in more than 70 genetic loci. The main causes of HSP development are mutations in the SPAST gene
REPLICATIVE STUDY OF GWAS-ASSOCIATED CANDIDATE GENE LOCI IN PATIENTS WITH OSTEOARTHRITIS FROM THE BASHKORTOSTAN REPUBLIC
TYURIN, A.V., SHAPOVALOVA, DARIA, DAVLETSHIN, RASHIT, KHUSAINOVA, RITA, LUKMANOVA, L.Z. (2019)
REPLICATIVE STUDY OF GWAS-ASSOCIATED CANDIDATE GENE LOCI IN PATIENTS WITH OSTEOARTHRITIS FROM

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