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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
MELATONIN PROTECTS BONE MARROW MESENCHYMAL STEM CELLS AGAINST IRON OVERLOAD-INDUCED ABERRANT DIFFERENTIATION AND SENESCENCE
Yang, F., Yang, L., Li, Y., Yan, G., Feng, C., Liu, T., Gong, R., Yuan, Y., Wang, N., Idiiatullina, E., Bikkuzin, T., V.N. Pavlov, Li, Y., Dong, C. (2017)
A HYBRID FC-FUSED HUMAN GROWTH HORMONE, GX-H9, SHOWS A POTENTIAL FOR WEEKLY AND TWICE-MONTHLY ADMINISTRATION IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
Mykola, A., Malievskiy, O, Nataliya, Z, Bolshova, EV, Senatorova, G, Oroszlan, G, Skorodok, J, Peterkova, V, Nataliya, C, Sorokman, T, Yang, S, Lee, JE, Muzsnai, A, Hwang, JS, Kim, T, Choi, YJ, Woo, J, Jang, WI, Sung, YC, Keyoung, M (2017)
Role of Optical Coherence Tomography in Diagnosis and Treatment of Patients with Acute Coronary Syndrome
Afolabi, A., Hu, SN., Wang, C., Zhu, YC., Mustafina, I., Lin, L., Zheng, GH., Zhe, CY., Jia, HB., Hou, JB., Yu, B. (2017)
LONG-QT SYNDROME-ASSOCIATED CAVEOLIN-3 MUTATIONS DIFFERENTIALLY REGULATE THE HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE GATED CHANNEL 4
Motloch, L.J., Larbig, R., Darabi, T., Reda, S., Motloch, K.A., Wernly, B., Lichtenauer, M., Gebing, T., Schwaiger, A., Zagidullin, N., Wolny, M., Hoppe, U.C. (2017)
with HCN4 and wild-type (WT) cav-3 or a LQTS-associated cav-3 mutant (T78M, A85T, S141R, or F97C). HCN4
LONG-ACTING C-TERMINAL PEPTIDE-MODIFIED HGH (MOD-4023): RESULTS OF A SAFETY AND DOSE-FINDING STUDY IN GHD CHILDREN
Zelinska, N., Iotova, V., Skorodok, J., Malievsky, O., Peterkova, V., Samsonova, L., Rosenfeld, Ron G., Zadik, Zvi, Jaron-Mendelson, Michal, Koren, Ronit, Amitzi, Leanne, Raduk, Dmitri, Hershkovitz, Oren, Hart, Gili (2017)
low compliance as a result of inconvenience and distress in patients. Objective: C-terminal peptide
EFFECTS OF BLUE LIGHT EMITTING DIODE IRRADIATION ON THE PROLIFERATION, APOPTOSIS AND DIFFERENTIATION OF BONE MARROW-DERIVED MESENCHYMAL STEM CELLS
Yuan, Y., Yan, G., Gong, R., Zhang, L., Liu, T., Feng, C., Du, W., Wang, Y., Yang, F., Li, Y., Guo, S., Ding, F., Ma, W., Idiiatullina, E., V.N. Pavlov, Han, Z., Cai, B., Yang, L. (2017)
REACTION OF PAEONIFLORIN WITH LOWER ALCOHOLS IN THE PRESENCE OF CATION EXCHANGER
Baltina, L.A., Shabieva, E.R., Kondratenko, R.M., Spirikhin, L.V., Baltina, L.A. (2017)
isolated as the tetra-O-acetates. The structures of the obtained compounds were confirmed using PMR and 13C
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 developing of chronic urticaria, rs2243250*C allele of the IL4 gene - of the acute urticaria, and the rs
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)
,51, respectively) in Tatar ethnicity. There is the association of allele rs1799836*C of the MAO-B gene with PD

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