Search Results - "Chernushyn, S. Yu"

ANALYSIS CYP21A2 GENE MUTATIONS TECHNIQUE IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA by Chernushyn, S Yu, Livshits, L A

“…In this paper, the technique of CYP21A2 gene mutation analysis, which can be applicable for pre- and postnatal diagnosis of congenital adrenal hyperplasia…”
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IFNL4 polymorphism as a predictor of chronic hepatitis C treatment efficiency in Ukrainian patients by Kucherenko, A. M., Pampukha, V. M., Romanchuk, K. Yu, Chernushyn, S. Yu, Bobrova, I. A., Moroz, L. V., Livshits, L. A.

“…The aim of this study was to examine association between IFNL4 gene ss469415590 and treatment efficiency in group of Ukrainian PEG-interferon/ribavirin-treated…”
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Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients by Chernushyn, S. Yu, Hryshchenko, N. V.

“…Prader-Willi (PWS) and Angelman (AS) syndromes are two clinically distinct genetic diseases associated with multiple physical and cognitive abnormalities. The…”
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Identification and characterization of the SARS-CoV-2 lineage B.1.1.7 upon the new outbreak of the COVID-19 in Ukraine in February 2021 by Kashuba, V. I., Hryshchenko, N. V., Gerashchenko, G. V., Melnichuk, N. S., Marchishak, T. V., Chernushyn, S. Yu, Chernenko, L. M., Liashko, V. K., Tkachuk, Z. Yu, Tukalo, M. A.

“…Aim. To identify and characterize the SARS-CoV-2 variants, collected upon the new wave of COVID-19 outbreak in Ivano-Frankivs’k region of Ukraine, using the…”
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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis by Livshits, L. A., Kravchenko, S. A., Nechyporenko, M. V., Pampukha, V. M., Hryshchenko, N. V., Livshyts, G. B., Soloviov, O. O., Tatarskyy, P. F., Fesai, O. A., Chernushyn, S. Yu, Kucherenko, A. M., Gulkovskyy, R. V.

“…The summarized results of 25-year studies of department of human genomics of IMBG NASU are presented. The investigations were focused on identification of…”
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Analysis of CYP21A2 gene mutations in patients from Ukraine with congenital adrenal hyperplasia by Chernushyn, S. Yu, Livshits, L. A.

“…In the article, the data on the distribution of CYP21A2 gene mutations (gene deletion/conversion, c.290-13C>A/G, E110Vfs, I172N, cluster of mutations I236N,…”
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Development of MLPA approach for SNP detection in MTHFR, F and F2 genes by Kravchenko, S. A., Chernushyn, S. Yu, Kucherenko, A. M., Soloviov, O. O., Livshits, L. A.

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Development of MLPA approach for SNP detection in MTHFR, F5and F2genes by Kravchenko, S A, Yu, Chernushyn S, Kucherenko, A M, Soloviov, O O, Livshits, L A

“…Single nucleotide polymorphism (SNP) is an important and valuable form of DNA variation among individuals. Various methods for SNP genotyping have been…”
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