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dc.contributor.authorCho, Soo Min-
dc.contributor.authorLee, Sejin-
dc.contributor.authorYang, Seung-Hoon-
dc.contributor.authorKim, Hye Yun-
dc.contributor.authorLee, Michael Jisoo-
dc.contributor.authorKim, Hyunjin Vincent-
dc.contributor.authorKim, Jiyoon-
dc.contributor.authorBaek, Seungyeop-
dc.contributor.authorYun, Jin-
dc.contributor.authorKim, Dohee-
dc.contributor.authorKim, Yun Kyung-
dc.contributor.authorCho, Yakdol-
dc.contributor.authorWoo, Jiwan-
dc.contributor.authorKim, Tae Song-
dc.contributor.authorKim, YoungSoo-
dc.date.accessioned2024-01-20T05:01:29Z-
dc.date.available2024-01-20T05:01:29Z-
dc.date.created2022-01-10-
dc.date.issued2016-02-02-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124403-
dc.description.abstractAmyloid-beta (A beta) plays a critical role as a biomarker in Alzheimer's disease (AD) diagnosis. In addition to its diagnostic potential in the brain, recent studies have suggested that changes of A beta level in the plasma can possibly indicate AD onset. In this study, we found that plasma A beta(1-42) concentration increases with age, while the concentration of A beta(1-42) in the cerebrospinal fluid (CSF) decreases in APP(swe), PS1(M146V) and Tau(P301L) transgenic (3xTg-AD) mice, if measurements were made before formation of ThS-positive plaques in the brain. Our data suggests that there is an inverse correlations between the plasma and CSF A beta(1-42) levels until plaques form in transgenic mice's brains and that the plasma A beta concentration possesses the diagnostic potential as a biomarker for diagnosis of early AD stages.-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectMILD COGNITIVE IMPAIRMENT-
dc.subjectA-BETA-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectDEMENTIA-
dc.subjectRISK-
dc.subjectMODEL-
dc.subjectASSOCIATION-
dc.subjectBIOMARKERS-
dc.subjectDEFICITS-
dc.subjectDECLINE-
dc.titleAge-dependent inverse correlations in CSF and plasma amyloid-beta(1-42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice-
dc.typeArticle-
dc.identifier.doi10.1038/srep20185-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.6-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume6-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000369090500001-
dc.identifier.scopusid2-s2.0-84957595802-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.type.docTypeArticle-
dc.subject.keywordPlusMILD COGNITIVE IMPAIRMENT-
dc.subject.keywordPlusA-BETA-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusDEMENTIA-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusBIOMARKERS-
dc.subject.keywordPlusDEFICITS-
dc.subject.keywordPlusDECLINE-
dc.subject.keywordAuthor치매-
dc.subject.keywordAuthor알츠하이머-
dc.subject.keywordAuthor혈액진단-
dc.subject.keywordAuthordementia-
dc.subject.keywordAuthorAlzheimer-
dc.subject.keywordAuthorblood test-
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KIST Article > 2016
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