Identification of genes related to Parkinson's disease using expressed sequence tags

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dc.contributor.authorJ M Kim-
dc.contributor.authorKyu-Hwa Lee-
dc.contributor.authorYeo-Jin Jeon-
dc.contributor.authorJ H Oh-
dc.contributor.authorSo-Young Jeong-
dc.contributor.authorIn Sung Song-
dc.contributor.authorJ M Kim-
dc.contributor.authorD S Lee-
dc.contributor.authorNam-Soon Kim-
dc.date.accessioned2017-04-19T09:06:47Z-
dc.date.available2017-04-19T09:06:47Z-
dc.date.issued2006-
dc.identifier.issn1340-2838-
dc.identifier.uri10.1093/dnares/dsl016ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7838-
dc.description.abstractIn a search for novel target genes related to Parkinson's disease (PD), two full-length cDNA libraries were constructed from a human normal substantia nigra (SN) and a PD patient's SN. An analysis of the gene expression profiles between them was done using the expressed sequence tags (ESTs) frequency. Data for the differently expressed genes were verified by quantitative real-time RT-PCR, immunohistochemical analysis and a cell death assay. Among the 76 genes identified with a significant difference (P > 0.9), 21 upregulated genes and 13 downregulated genes were confirmed to be differentially expressed in human PD tissues and/or in an MPTP-treated mice model by quantitative real-time RT-PCR. Among those genes, an immunohistochemical analysis using an MPTP mice model for alpha-tubulin including TUBA3 and TUBA6 showed that the protein levels are downregulated, as well as the RNA levels. In addition, MBP, PBP and GNAS were confirmed to accelerate cell death activity, whereas SPP1 and TUBA3 to retard this process. Using an analysis of ESTs frequency, it was possible to identify a large number of genes related to human PD. These new genes, MBP, PBP, GNAS, SPP1 and TUBA3 in particular, represent potential biomarkers for PD and could serve as useful targets for elucidating the molecular mechanisms associated with PD.-
dc.publisherOxford Univ Press-
dc.titleIdentification of genes related to Parkinson's disease using expressed sequence tags-
dc.title.alternativeIdentification of genes related to Parkinson's disease using expressed sequence tags-
dc.typeArticle-
dc.citation.titleDNA Research-
dc.citation.number6-
dc.citation.endPage286-
dc.citation.startPage275-
dc.citation.volume13-
dc.contributor.affiliatedAuthorKyu-Hwa Lee-
dc.contributor.affiliatedAuthorYeo-Jin Jeon-
dc.contributor.affiliatedAuthorSo-Young Jeong-
dc.contributor.affiliatedAuthorIn Sung Song-
dc.contributor.affiliatedAuthorNam-Soon Kim-
dc.contributor.alternativeName김정민-
dc.contributor.alternativeName이규화-
dc.contributor.alternativeName전여진-
dc.contributor.alternativeName오정화-
dc.contributor.alternativeName정소영-
dc.contributor.alternativeName송인성-
dc.contributor.alternativeName김진만-
dc.contributor.alternativeName이동석-
dc.contributor.alternativeName김남순-
dc.identifier.bibliographicCitationDNA Research, vol. 13, no. 6, pp. 275-286-
dc.identifier.doi10.1093/dnares/dsl016-
dc.subject.keywordCell death-
dc.subject.keywordExpressed sequence tags-
dc.subject.keywordGene expression profiling-
dc.subject.keywordImmunohistochemistry-
dc.subject.keywordParkinson's disease-
dc.subject.localCell death-
dc.subject.localcell death-
dc.subject.localExpressed sequence tag-
dc.subject.localExpressed sequence tags-
dc.subject.localExpressed sequence tags (ESTs)-
dc.subject.localexpressed sequence tag-
dc.subject.localexpressed sequence tag (EST)-
dc.subject.localexpressed sequence tags-
dc.subject.localGene expression profiling-
dc.subject.localGene expression profiling.-
dc.subject.localgene expression profiling-
dc.subject.localImmunohistochemistry-
dc.subject.localimmunohistochemistry-
dc.subject.localimmunohistochimistry-
dc.subject.localParkinson disease-
dc.subject.localParkinson's disease-
dc.subject.localParkinson’s Disease-
dc.subject.localParkinson’s disease-
dc.subject.localParkinson’s diseases-
dc.subject.localParkinsons disease (PD)-
dc.subject.localParkinsons disease-
dc.subject.localParkinson's diasease-
dc.subject.localParkinson's Disease-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
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