Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/100107
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dc.titleApplication of zebrafish microarray on the toxicity mechanism study of bisphenol A
dc.contributor.authorDuan, Z.-H.
dc.contributor.authorZhu, L.
dc.contributor.authorFeng, M.-F.
dc.contributor.authorBu, W.-J.
dc.contributor.authorLam, S.-H.
dc.contributor.authorGong, Z.-Y.
dc.date.accessioned2014-10-27T08:22:05Z
dc.date.available2014-10-27T08:22:05Z
dc.date.issued2010-03
dc.identifier.citationDuan, Z.-H.,Zhu, L.,Feng, M.-F.,Bu, W.-J.,Lam, S.-H.,Gong, Z.-Y. (2010-03). Application of zebrafish microarray on the toxicity mechanism study of bisphenol A. Huanjing Kexue/Environmental Science 31 (3) : 808-814. ScholarBank@NUS Repository.
dc.identifier.issn02503301
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/100107
dc.description.abstractThe toxicity mechanism of bisphenol A (BPA) to zebrafish (Danio rerio) was studied in the molecular level, by the method of zebrafish microarray and quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR). Zebrafish embryos were exposed to 0.5, 1.5 and 4.5 mg/L BPA for 8 days since fertilization. The results from microarray and validated by qRT-PCR showed that, 50 specific genes were up-or down-regulated, and dose-responses for them were significant (p < 0.05). This study demonstrates the genotoxicity of BPA. Moreover, according to their function and pathway analysis, it could support the mechanisms for the morphological toxicity and metabolize turbulence observed in prophase study.
dc.sourceScopus
dc.subjectBisphenol A (BPA)
dc.subjectMechanisms
dc.subjectQuantitative real-time RT-PCR
dc.subjectToxicity
dc.subjectZebrafish microarray
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.sourcetitleHuanjing Kexue/Environmental Science
dc.description.volume31
dc.description.issue3
dc.description.page808-814
dc.description.codenHCKHD
dc.identifier.isiutNOT_IN_WOS
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