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dc.contributor.author손형진*
dc.contributor.author현동훈*
dc.date.accessioned2016-08-28T12:08:09Z-
dc.date.available2016-08-28T12:08:09Z-
dc.date.issued2011*
dc.identifier.issn1567-7249*
dc.identifier.otherOAK-7898*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221896-
dc.description.abstractThe nature of mitochondrial dysfunction in dopaminergic neurons in familial Parkinson's disease (PD) is unknown. We characterized the pathophenotypes of dopaminergic neuronal cells that were deficient in PINK1 or DJ-1, genes with mutations linked to familial PD. Both PINK1- and DJ-1-deficient dopaminergic neurons had the increased production of ROS, severe mitochondrial structural damages and complex I deficits. A striking decrease in complex IV activity was also prominent by the PINK1-deficiency. The complex I deficits were relatively PD-specific and were significantly improved by an antioxidant Trolox. These data suggest that mitochondrial deficits are severe in dopaminergic neurons in familial PD and antioxidant-mediated functional recovery is feasible. © 2011.*
dc.languageEnglish*
dc.titleThe antioxidant Trolox helps recovery from the familial Parkinson's disease-specific mitochondrial deficits caused by PINK1- and DJ-1-deficiency in dopaminergic neuronal cells*
dc.typeArticle*
dc.relation.issue5*
dc.relation.volume11*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage707*
dc.relation.lastpage715*
dc.relation.journaltitleMitochondrion*
dc.identifier.doi10.1016/j.mito.2011.05.013*
dc.identifier.wosidWOS:000294089000005*
dc.identifier.scopusid2-s2.0-79961207215*
dc.author.googleShim J.H.*
dc.author.googleYoon S.H.*
dc.author.googleKim K.-H.*
dc.author.googleHan J.Y.*
dc.author.googleHa J.-Y.*
dc.author.googleHyun D.H.*
dc.author.googlePaek S.H.*
dc.author.googleKang U.J.*
dc.author.googleZhuang X.*
dc.author.googleSon J.H.*
dc.contributor.scopusid손형진(7203086503)*
dc.contributor.scopusid현동훈(7005049041)*
dc.date.modifydate20240123112641*
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약학대학 > 약학과 > Journal papers
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