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dc.contributor.authorPrysyazhnyuk, Vasyl-
dc.contributor.authorVoloshyn, Olexander-
dc.contributor.authorPrysiazhniuk, Iryna-
dc.contributor.authorIlashchuk, Tetiana-
dc.contributor.authorSydorchuk, Larysa-
dc.contributor.authorPrysyazhnyuk, Petro-
dc.date.accessioned2025-02-25T10:14:01Z-
dc.date.available2025-02-25T10:14:01Z-
dc.date.issued2020-
dc.identifier.otherDOI: https://doi.org/10.5114/ceh.2020.95678-
dc.identifier.urihttp://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/26220-
dc.description.abstractAim of the study: Among the key genes involved in the development of non-alcoholic fatty liver disease (NAFLD) are genes encoding the synthesis of glutathione S-transferase (GST). Conclusions: Deletion polymorphism of GSTT1 and GSTM1 genes distribution among NAFLD patients did not differ as compared to healthy individuals. Null-genotype GSTT1 gene carriers were characterized by higher TNF-α concentration and null-genotype GSTM1 gene carriers were characterized by elevated leptin level as compared to normal genotype carriers.uk_UA
dc.language.isoenuk_UA
dc.publisherClinical and Experimental Hepatology (офіційний журнал Польської асоціації з вивчення печінки)uk_UA
dc.subjectnon-alcoholic fatty liver diseaseuk_UA
dc.subjectglutathione S-transferase geneuk_UA
dc.subjectleptinuk_UA
dc.subjectadiponectinuk_UA
dc.titleGlutathione S-transferase T1 and M1 null genotype distribution among non-alcoholic fatty liver disease patients and its association with cytokine and adipokine profilesuk_UA
dc.typeArticleuk_UA
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