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Application of multiplex bead array assay for Yq microdeletion analysis in infertile males

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dc.contributor.authorYeom, Hye-Jung-
dc.contributor.authorHer, Young-Sun-
dc.contributor.authorOh, Moon-Ju-
dc.contributor.authorPaul, Saswati-
dc.contributor.authorPark, Mi-Seon-
dc.contributor.authorYeoun, Jong-Pil-
dc.contributor.authorJung, Jin-Wook-
dc.contributor.authorLee, Suman-
dc.contributor.authorHwang, Seung Yong-
dc.date.accessioned2021-06-23T17:41:45Z-
dc.date.available2021-06-23T17:41:45Z-
dc.date.issued2008-04-
dc.identifier.issn0890-8508-
dc.identifier.issn1096-1194-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/42580-
dc.description.abstractThe purpose of this study was to apply the multiplex bead array as a diagnostic tool for male infertility. The multiplex bead array offers a new platform in high-throughput nucleic acid detection. Six loci, including sex-determining regions on the Y (SRY) chromosome as a control and five sequence-tagged sites (STS) in azoospermia-factor regions, were used in this system. Extracted genomic DNA from infertile male blood was used for multiplex polymerase chain reaction (PCR). After multiplex PCR using specific Cy3-labeled primer sets, the PCR product was hybridized with capture probes. A multiplexed PCR-liquid bead was arrayed for simultaneous detection using the Luminex system. This assay system correctly identified the presence or deletion of the Y chromosome. Therefore, this method provides a sensitive and high-throughput method for probing the deletion of the Y chromosome, and offers a completely new approach to male infertility screening. (C) 2007 Elsevier Ltd. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleApplication of multiplex bead array assay for Yq microdeletion analysis in infertile males-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.mcp.2007.06.004-
dc.identifier.scopusid2-s2.0-40149103441-
dc.identifier.wosid000264314400002-
dc.identifier.bibliographicCitationMolecular and Cellular Probes, v.22, no.2, pp 76 - 82-
dc.citation.titleMolecular and Cellular Probes-
dc.citation.volume22-
dc.citation.number2-
dc.citation.startPage76-
dc.citation.endPage82-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCHROMOSOME-
dc.subject.keywordPlusMEN-
dc.subject.keywordPlusTECHNOLOGY-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusAZOOSPERMIA-
dc.subject.keywordPlusDELETIONS-
dc.subject.keywordPlusPROFILES-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordAuthorInfertile-
dc.subject.keywordAuthorLuminex-
dc.subject.keywordAuthorMultiplex PCR-
dc.subject.keywordAuthorSTS markers-
dc.subject.keywordAuthorY chromosome-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0890850807000540?via%3Dihub-
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ERICA 첨단융합대학 (ERICA 분자의약전공)
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