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dc.contributor.author황승용-
dc.date.accessioned2023-05-31T00:19:38Z-
dc.date.available2023-05-31T00:19:38Z-
dc.date.issued2016-03-
dc.identifier.citationMolecular & Cellular Toxicology, v. 12, NO. 1, Page. 15-20-
dc.identifier.issn1738-642X;2092-8467-
dc.identifier.urihttps://link.springer.com/article/10.1007/s13273-016-0003-4en_US
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/181585-
dc.description.abstractXylene is volatile organic compound that has been reported to increase the incidence of cancer and various diseases related to the immune system, cardiovascular systems, respiratory and reproductive organs. However, there are currently few biomarkers in human cases. Using microarray, we analysed 10 participants for the xylene-exposure group and 10 controls that were not exposed to xylene. The two groups were compared in terms of expression levels and methylation patterns. We identified 6 genes that were down-regulated and hyper-methylated, and 132 that were up-regulated and hypo-methylated in the xylene-exposure group compared to control. We sorted out and 28 biomarker candidates were chosen using DAVID. And then, we used IPA to select the significant potential biomarkers in them. We used network analysis and selected 6 significant genes, and these 6 genes showed altered expression and methylation in xylene-exposure group, suggesting that they are suitable potential biomarkers for xylene exposure.-
dc.description.sponsorshipthe Korea University Medical Center (IRB #AS 14039) and microarray data analysis was carried out at BioCore Co. (Seoul, Korea). This study was supported by the Korean Ministry of Environment as a Converging Technology Project (no. 201400165002).-
dc.languageen-
dc.publisher대한독성 유전단백체 학회-
dc.subjectXylene-
dc.subjectMicroarray-
dc.subjectGene expression-
dc.subjectMethylation-
dc.subjectBiomarker-
dc.titleIdentification of potential biomarkers for xylene exposure by microarray analyses of gene expression and methylation-
dc.typeArticle-
dc.relation.no1-
dc.relation.volume12-
dc.identifier.doi10.1007/s13273-016-0003-4-
dc.relation.page15-20-
dc.relation.journalMolecular & Cellular Toxicology-
dc.contributor.googleauthorKim, Seol Young-
dc.contributor.googleauthorHong, Ji Young-
dc.contributor.googleauthorYu, So-Yeon-
dc.contributor.googleauthorKim, Gi Won-
dc.contributor.googleauthorAhn, Jeong Jin-
dc.contributor.googleauthorKim, Youngjoo-
dc.contributor.googleauthorSon, Sang Wook-
dc.contributor.googleauthorPark, Jong-Tae-
dc.contributor.googleauthorHwang, Seung Yong-
dc.sector.campusE-
dc.sector.daehak과학기술융합대학-
dc.sector.department의약생명과학과-
dc.identifier.pidsyhwang-
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E](과학기술융합대학) > ETC
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