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Gene expression profiles of rat olfactory bulb at developmental stage

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dc.contributor.authorCho, Jae Hoon-
dc.contributor.authorJung, Hak Hyun-
dc.contributor.authorLee, Sang Hak-
dc.contributor.authorIm, Gi Jung-
dc.contributor.authorChang, Jiwon-
dc.contributor.authorKim, Seo Jin-
dc.date.accessioned2021-09-08T19:39:29Z-
dc.date.available2021-09-08T19:39:29Z-
dc.date.created2021-06-19-
dc.date.issued2009-02-15-
dc.identifier.issn0165-0270-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120577-
dc.description.abstractMicroarray analysis may be a useful tool to identify some candidate genes related to the development of olfactory bulbs. In the present study, gene expression profiles of olfactory bulbs from postnatal day 1 (P1) rats and postnatal day 35 (P35) rats were analyzed by oligonucleotide-microarray and expression levels of some selected genes were also confirmed by RT-PCR and in situ hybridization. 9146 genes were commonly identified in six microarray chips. Among these genes, 76 were up-regulated and 130 were down-regulated three-folds or more at P1 olfactory bulbs. Out of these 76 up-regulated genes, 24 genes were annotated based on the NCBI database of reference sequences and expression levels of these 24 genes were confirmed by RT-PCR. Among them, 2 interesting genes (neurogenic differentiation 1 and retinoid acid receptor alpha) were localized in the PI olfactory bulb by the use of in situ hybridization technique. Our results may provide basic information to identify genes associated with functional growth of olfactory bulbs. (C) 2008 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.subjectCANDIDATE GENES-
dc.subjectBINDING-PROTEIN-
dc.subjectCDNA CLONING-
dc.subjectNEURONS-
dc.subjectIDENTIFICATION-
dc.subjectFAMILY-
dc.titleGene expression profiles of rat olfactory bulb at developmental stage-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Hak Hyun-
dc.contributor.affiliatedAuthorIm, Gi Jung-
dc.identifier.doi10.1016/j.jneumeth.2008.09.012-
dc.identifier.scopusid2-s2.0-57849103869-
dc.identifier.wosid000262706300002-
dc.identifier.bibliographicCitationJOURNAL OF NEUROSCIENCE METHODS, v.177, no.1, pp.14 - 19-
dc.relation.isPartOfJOURNAL OF NEUROSCIENCE METHODS-
dc.citation.titleJOURNAL OF NEUROSCIENCE METHODS-
dc.citation.volume177-
dc.citation.number1-
dc.citation.startPage14-
dc.citation.endPage19-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusCANDIDATE GENES-
dc.subject.keywordPlusBINDING-PROTEIN-
dc.subject.keywordPlusCDNA CLONING-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordAuthorOlfactory bulb-
dc.subject.keywordAuthorDevelopment-
dc.subject.keywordAuthorGene expression-
dc.subject.keywordAuthorRat-
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