Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/1099
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dc.contributor.authorDamnjanović, Tatjanaen_US
dc.contributor.authorLuković, Ljiljanaen_US
dc.contributor.authorCvetković, Draganaen_US
dc.contributor.authorJekić, Biljanaen_US
dc.contributor.authorBunjevački, Veraen_US
dc.contributor.authorMaksimović, Nelaen_US
dc.contributor.authorCvjeticanin, Suzanaen_US
dc.contributor.authorMajkić-Singh, Nadaen_US
dc.contributor.authorSlavko, S.en_US
dc.contributor.authorNovaković, Ivanaen_US
dc.date.accessioned2019-07-24T12:12:05Z-
dc.date.available2019-07-24T12:12:05Z-
dc.date.issued2014-01-01-
dc.identifier.issn0354-4664-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/1099-
dc.description.abstractThe effect of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism on serum lipid profiles is controversial. We randomly selected 530 healthy schoolchildren that were included in the Yugoslav Study of the Precursors of Atherosclerosis in School Children (YUSAD). The detected frequencies of MTHFR 677TT genotypes and MTHFR 677T allele were 13.4% and 35.5%, respectively. The mean levels of total cholesterol, low-density lipoprotein cholesterol and triglycerides were higher and high-density lipoprotein cholesterol was lower in the group of children with TT genotype compared with remaining genotypes. All differences were without statistical significance. Our findings suggest that there is no influence of MTHFR C677T gene variants on the lipid parameters in the population of Serbian children.en_US
dc.language.isoenen_US
dc.publisherInstitut za Bioloska Istrazivanjaen_US
dc.relation.ispartofArchives of Biological Sciencesen_US
dc.subjectAtherosclerosisen_US
dc.subjectLipid levelsen_US
dc.subjectMTHFR 677T alleleen_US
dc.subjectMTHFR geneen_US
dc.subjectPolymorphismen_US
dc.subjectSchoolchildrenen_US
dc.titlePossible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school childrenen_US
dc.typeArticleen_US
dc.identifier.doi10.2298/ABS1402729D-
dc.identifier.scopus2-s2.0-84904010981-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84904010981-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of Genetics and Evolution-
crisitem.author.orcid0000-0002-1311-7481-
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