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dc.contributor.author현동훈*
dc.date.accessioned2016-08-28T12:08:51Z-
dc.date.available2016-08-28T12:08:51Z-
dc.date.issued2010*
dc.identifier.issn0304-3940*
dc.identifier.otherOAK-6302*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220558-
dc.description.abstractThe objective of the present study was to examine the role of selenium in the metabolism of Aβ and in Aβ-induced neuronal death. Selenium treatment significantly reduced Aβ40, Aβ42, and sAPPβ production by reducing Aβ producing β-secretase and γ-secretase activities. The lipid peroxidation product 4-Hydroxynonenal (HNE)-induced transcription of β-secretase (BACE1) was blocked by selenium. Finally, our data show that selenium protects against HNE and Aβ-mediated toxicity in primary cultured neurons. The present study suggests that selenium may be able to salvage the neuronal degeneration of Alzheimer's disease, thereby limiting β-amyloid production and neuronal death. © 2009 Elsevier Ireland Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSelenium attenuates Aβ production and Aβ-induced neuronal death*
dc.typeArticle*
dc.relation.issue3*
dc.relation.volume469*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage391*
dc.relation.lastpage395*
dc.relation.journaltitleNeuroscience Letters*
dc.identifier.doi10.1016/j.neulet.2009.12.035*
dc.identifier.wosidWOS:000274722100023*
dc.identifier.scopusid2-s2.0-73649138850*
dc.author.googleGwon A.-R.*
dc.author.googlePark J.-S.*
dc.author.googlePark J.-H.*
dc.author.googleBaik S.-H.*
dc.author.googleJeong H.-Y.*
dc.author.googleHyun D.-H.*
dc.author.googlePark K.W.*
dc.author.googleJo D.-G.*
dc.contributor.scopusid현동훈(7005049041)*
dc.date.modifydate20240123112641*
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자연과학대학 > 생명과학전공 > Journal papers
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