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EVALUATION OF TISSUE METAL AND TRACE ELEMENT CONTENT IN A RAT MODEL OF NON-ALCOHOLIC FATTY LIVER DISEASE USING ICP-DRC-MS
Gatiatulinaa, E.R., Popova, E.V., Polyakova, V.S., Skalnaya, A.A., Agletdinovd, E.F., Nikonorovae, A.A., Skalnyefgh, A.V., Tinkov, A.A. (2017)
The primary objective of the study was to assess the level of metals and trace elements in liver
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)
and children. The present trial was a safety and dose-finding study for weekly MOD-4023 in GHD children. Design
A RANDOMIZED PHASE 2 STUDY OF LONG-ACTING TRANSCON GH VS DAILY GH IN CHILDHOOD GH DEFICIENCY
Chatelain, Pierre, Malievskiy, Oleg, Radziuk, Klaudziya, Senatorova, Ganna, Abdou, Magdy O., Vlachopapadopoulou, Elpis, Skorodok, Yulia, Peterkova, Valentina, Leff, Jonathan A., Beckert, Michael (2017)
children with GHD. Design: Randomized, open-label, active-controlled study of three doses of weekly Trans
THE OFF-LABEL USE OF DRUGS FOR PARENTERAL NUTRITION AS A SOLVENT OF SUBSTANCES SLIGHTLY SOLUBLE IN WATER IN PHARMACOLOGICAL RESEARCH
Urakov, A.L., Mustafin, I.G., Samorodov, A.V., Kamilov, F.K., Khaliullin, F.A. (2017)
of preclinical and clinical studies, the research work enabled to develop the original solvent for poorly soluble
THE ASSOCIATION OF THE PTPN22 RS2476601 GENE POLYMORPHISM WITH JUVENILE IDIOPATHIC ARTHRITIS IN CHILDREN FROM RUSSIA
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2017)
factors [1]. The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene single
ФИЗИЧЕСКАЯ ПОДГОТОВЛЕННОСТЬ, МОРФОФУНКЦИОНАЛЬНОЕ СОСТОЯНИЕ И ПИЩЕВОЙ СТАТУС СТУДЕНТОВ(ОК) ИНДИИ, ТАДЖИКИСТАНА, НИГЕРИИ, ПРИЕХАВШИХ НА УЧЕБУ В БАШКОРТОСТАН
PHYSICAL FITNESS, MORPHOFUNCTIONAL STATE, AND NUTRITIONAL STATUS OF INDIAN, TAJIK, AND NIGERIAN STUDENTS STUDYING IN BASHKORTOSTAN
Гайнуллин, Р.А., Акинйеми, С., Gainullin, R.A., Akinyemi, S. (2017)
Aim. To study effects of regional factors and strenuous educational process on cardiorespiratory
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)
. According to epidemiological studies, at least once during a lifetime this pathology is observed in 15
THE «IN VIVO» STUDY OF BLOOD 5-FLUOROURACIL CONTENT BY QUENCHING OF INTRINSIC PROTEIN FLUORESCENCE
Kayumova, R.R., Sultanbaev, A.V., Ostakhov, S.S., Khursan, S.L., Abdullin, M.F., Gantsev, S.K., Sakaeva, D.D. (2017)
THE «IN VIVO» STUDY OF BLOOD 5-FLUOROURACIL CONTENT BY QUENCHING OF INTRINSIC PROTEIN FLUORESCENCE
ADVANCES IN THE CHEMISTRY OF NATURAL AND SEMISYNTHETIC TOPOISOMERASE I/II INHIBITORS
Дьяконов, В.А., Джемилева, Л.У., Джемилев, У.М., D'yakonov, V.A., Dzhemileva, L.U., Dzhemilev, U.M. (2017)
studies in this field have shown that topoisomerases I and II are one of the main molecular targets
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)
-q12) associated with congenital non-syndromic autosomal recessive deafness. This mutation

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