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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/48087
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dc.contributor.authorGolovchenko, O. V.-
dc.contributor.authorAbramova, M. Yu.-
dc.contributor.authorOrlova, V. S.-
dc.contributor.authorBatlutskaya, I. V.-
dc.contributor.authorSorokina, I. N.-
dc.date.accessioned2022-10-19T13:40:54Z-
dc.date.available2022-10-19T13:40:54Z-
dc.date.issued2022-
dc.identifier.citationClinical and genetic characteristics of preeclampsia / O.V. Golovchenko [et al.] // Archives of Razi Institute. - 2022. - Vol.77, №1.-P. 293-299. - Doi: 10.22092/ARI.2021.356481.1852. - Refer.: p. 298-299.ru
dc.identifier.urihttp://dspace.bsu.edu.ru/handle/123456789/48087-
dc.description.abstractPreeclampsia (PE) is a severe complication of pregnancy accompanied by arterial hypertension, edema, or proteinuria with impaired functioning of various organs and systems. Recently, many scientists have especially focused on the study of genetic factors underlying the etiopathogenesis of PE, namely, the contribution of individual polymorphic loci of various candidate genes. The current study aimed to investigate the clinical characteristics of PE and the contribution of the polymorphic loci rs1042838 of Progesterone Receptor (PGR) gene and rs8068318 of the T-Box Transcription Factor 2 (TBX2) gene to the development of PEru
dc.language.isoenru
dc.subjectmedicineru
dc.subjectmedical geneticsru
dc.subjectedemaru
dc.subjectpreeclampsiaru
dc.subjectpolymorphic locusru
dc.subjectproteinuriaru
dc.subjectrs1042838 PGRru
dc.subjectrs8068318ru
dc.subjectTBX2ru
dc.titleClinical and genetic characteristics of preeclampsiaru
dc.typeArticleru
Appears in Collections:Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)

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