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dc.contributor.authorHuang, GSen_US
dc.contributor.authorHung, YCen_US
dc.contributor.authorChen, Aen_US
dc.contributor.authorHong, MYen_US
dc.date.accessioned2014-12-08T15:25:12Z-
dc.date.available2014-12-08T15:25:12Z-
dc.date.issued2005en_US
dc.identifier.isbn0-7803-9298-1en_US
dc.identifier.issn1062-922Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/17588-
dc.description.abstractMicroarray experiments were performed to normal ovaries, benign ovarian tumor and stage I and III of ovarian cancer. By treating benign ovarian tumor as pre-cancerous stage and comparing to later stages of ovarian cancer we identified 46 genes overly expressed in early-staged cancer. We also identified over-expressed genes at all stages of ovarian tumor/cancer. The over-expressed genes might be alternative candidates for developing early diagnostic markers. JUN and nuclear receptor subfamily genes were repeatedly identified in the group of down-regulated genes indicating their important regulatory roles in the oncogenesis of ovary.en_US
dc.language.isoen_USen_US
dc.subjectmicroarrayen_US
dc.subjectovarian canceren_US
dc.subjectgene expressionen_US
dc.subjectearly diagnostic markeren_US
dc.titleMicroarray analysis of ovarian canceren_US
dc.typeProceedings Paperen_US
dc.identifier.journalINTERNATIONAL CONFERENCE ON SYSTEMS, MAN AND CYBERNETICS, VOL 1-4, PROCEEDINGSen_US
dc.citation.spage1036en_US
dc.citation.epage1041en_US
dc.contributor.department材料科學與工程學系奈米科技碩博班zh_TW
dc.contributor.departmentGraduate Program of Nanotechnology , Department of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000235210801007-
Appears in Collections:Conferences Paper