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По вашему запросу найдено документов: 1793

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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)

of Eurasia was revealed. The analysis of the spectrum and frequency of mutations in genes GJB2, GJB6, GJB3

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

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)

Abstract Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent

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

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

SPECTRUM AND FREQUENCY OF THE GJB2 GENE PATHOGENIC VARIANTS IN A LARGE COHORT OF PATIENTS WITH HEARING IMPAIRMENT LIVING IN A SUBARCTIC REGION OF RUSSIA (THE SAKHA REPUBLIC)

Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause

Kaempferol attenuates streptozotocin-induced diabetic nephropathy by downregulating TRAF6 expression: The role of TRAF6 in diabetic nephropathy

Luo, W., Chen, X., Ye, L., Chen, X., Jia, W., Zhao, Y., Samorodov, A.V., Zhang, Y., Hu, X., Zhuang, F., Qian, J., Zheng, C., Liang, G., Wang, Y. (2021)

of diabetic nephropathy (DN). TRAF6 functions as a signal transducer in toll-like receptor 4 and NF-κB pro

Новые лекарственные препараты для офтальмологии на основе 6-метил-3-(тиетан-3-ил)урацила (экспериментальное исследование)

New drugs for ophthalmology based on 6-methyl-3-(thietan-3-yl)uracil (experimental research)

Gabdrakhmanova, A.F., Mesheryakova, S.A., Kildiyarov, F.K., Kurbanov, S.A., Мещерякова, С. А., Габдрахманова, А. Ф., Кильдияров, Ф. Х., Курбанов, С. А. (2021)

Purpose: develop of new drugs for ophthalmology based on 6-methyl-3-(thietan-3-yl

ALKBH5 regulates cardiomyocyte proliferation and heart regeneration by demethylating the mRNA of YTHDF1

Han, Z.B., Wang, X.X., Xu, Z.H., Cao, Y., Gong, R, Zagidullin, N., Sukhareva, N., Zhang, Y. (2021)

N-6-methyladenosine (m(6)A) RNA modification, a dynamic and reversible process, is essential

THIETANYL PROTECTION IN THE SYNTHESIS OF 1-ALKYL-8-AMINO-3-METHYL-3,7-DIHYDRO-1H-PURINE-2,6-DIONES

Khaliullin, F.A., Shabalina, Yu.V., Sharafutdinov, R.M. (2015)

1-Alkyl-8-bromo-3-methyl-7-(1,1-dioxo-1λ6-thietan-3-yl)-3,7-dihydro-1H-purine-2,6-diones reacted

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