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dc.contributor.author김양하*
dc.date.accessioned2018-05-18T08:15:23Z-
dc.date.available2018-05-18T08:15:23Z-
dc.date.issued2004*
dc.identifier.issn0141-5492*
dc.identifier.otherOAK-2512*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243250-
dc.description.abstractDiallyl sulfide (DAS) and diallyl disulfide (DADS) at 25 μg ml -1 decreased the benzo[a]pyrene (B[a]P)-induced colony growth inhibition of human epidermal keratinocytes. DAS and DADS decreased B[a]P-DNA and B[a]P-protein adducts by 65% and 49-55%, respectively. The B[a]P-induced ethoxyresorufin O-deethylase activity, a marker enzyme for cytochrome P450 1, was decreased from 3 to 1.7-1.9 nmol min -1 mg -1 microsomal protein by DAS and DADS treatments. The activity of glutathione S-transferase, a detoxifying enzyme for B[a]P, but was decreased by DADS, but was unaffected by DAS.*
dc.languageEnglish*
dc.titleInhibition of the benzo[a]pyrene-induced toxicity by allyl sulfides in human epidermal keratinocytes*
dc.typeArticle*
dc.relation.issue22*
dc.relation.volume26*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1701*
dc.relation.lastpage1706*
dc.relation.journaltitleBiotechnology Letters*
dc.identifier.doi10.1007/s10529-004-3738-2*
dc.identifier.wosidWOS:000225902000003*
dc.identifier.scopusid2-s2.0-12444344777*
dc.author.googleChun H.S.*
dc.author.googleHyun J.K.*
dc.author.googleKim Y.*
dc.author.googleHyun J.C.*
dc.contributor.scopusid김양하(8524160300)*
dc.date.modifydate20240123090847*
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신산업융합대학 > 식품영양학과 > Journal papers
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