Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability by Gulkovskyi, R.V., Volkova, L.S., Livshits, L.A.

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Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses by Tkach, I.R., Sosnina, K.O., Huleyuk, N.L., Terpylyak, O.I., Zastavna, D.V., Weise, A., Kosyakova, N., Liehr, T.

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Association of allelic polymorphisms of the Matrix Gla-protein system genes with acute coronary syndrome in the Ukrainian population by Garbuzova, V.Yu., Stroy, D.A., Dosenko, V.E., Obukhova, O.A., Atama, O.V.

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Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability by Gulkovskyi, R.V., Chernushyn, S.Y., Livshits, L.A.

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Cisplatin treatment of C6 rat glioma in vivo did not influence copy number alterations and growth pattern of tumor-derived resistant cells by Stepanenko, A.A., Baklaushev, V.P., Vassetzky, Y.S., Dmitrenko, V.V.

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13q Deletions detected by fluorescence in situ hybridization for diagnosis and prognosis of chronic lymphoproliferative neoplasms by Sitko, V.V., Misharina, J.A., Minchenko, J.M., Poluben, L.O., Dmitrenko, O.O., Silaiev, Y.O., Kostyukova, N.I., Tkachenko, O.V., Tovstogan, A.O., Polyanska, V.M., Lyashenko, L.O., Bebeshko, V.G.

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Титр інтерферону та 2', 5'-олігоаденілат-синтетазна активність у лімфоцитах тимусу щурів за гіпергастринемії, спричиненої омепразолом... by Компанець, І.В., Короткий, О.Г., Карповець, Т.П., Пилипенко, С.В., Нікольська, В.В., Остапченко, Л.І., Янковський, Д.С.

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Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability by Gulkovskyi, R.V., Livshits, L.A., Sivolob, A.V.

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The effect of antiviral substance 6-(2-morpholin-4-yl-ethyl)-6H-indolo [2,3-b]quinoxaline upon biomarkers of inflammation by Antonovych, G.V., Zholobak, N.M., Shibinska, M.O., Spivak, M.Ya.

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Autoantibodies against tyrosyl-tRNA synthetase and its separated domains at essential hypertension by Grom, M.Yu., Yakovenko, L.F., Granich, V.M., Dobrohod, A.S., Torbas, O.O., Radchenko, A.D., Sirenko, Yu.M., Sidorik, L.L., Kornelyuk, A.I.

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Migration of labeled bone marrow MSCs and skin fibroblasts after systemic and local transplantation in rat burn wound model by Shchegelskaya, E.A., Grigorieva, T.G., Omelchenko, E.A., Zabirnyk, A.S., Markelova, E.V., Panibrattseva, S.G., Borovoy, I.A., Gubina-Vaculik, G.I., Oleynik, G.A.

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Aberrant expression of metallothioneins in clear cell renal cell carcinomas by Rymar, V.I., Lototskaya, L.V., Kondratov, O.G., Stakhovsky, E.O., Kononenko, O.A., Kashuba, V.I.

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Efficiency of application of different DNA probes in identifying marker chromosomes by Tavokina, L.V., Brovko, A.O., Baronova, E.V., Moskalenko, E.P., Gorovenko, N.G.

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MiR-137 expression in neuroblastoma: a role in clinical course and outcome by Inomistova, M.V., Khranovska, N.M., Skachkova, O.V., Klymniuk, G.I., Demydov, S.V., Svergun, N.M.

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Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene by Trofimova, N.S., Olkhovich, N.V., Gorovenko, N.G.

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Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis I: identification of three new mutations in α-L-iduronidase gene by Trofimova, N.S., Olkhovich, N.V.

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The polymorphisms of genes involved in DNA methylation in patients with malignancies from West Ukraine by Dmytruk, I.M., Makukh, H.V., Thyrkus, M.Y., Kitsera, N.I.

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Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease by Mytsyk, N.Y., Gorovenko, N.G.

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Analysis of mutations in GBA gene in Ukrainian patients with Gaucher disease by Olkhovych, N.V., Nedoboy, A.M., Pichkur, N.O., Gorovenko, N.H.

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Single center study of ESBL-related strains of Enterobacteriaceae collected from clinical specimens of infants with the congenital heart disease using multiplex PCR amplification by Filonenko, G.V., Talalaiev, O.S., Kyryk, D.L., Kovalenko, N.O., Skorohod, I.M., Salamanina, A.O.

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