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Specific monitoring of cardiomyogenic and endothelial differentiation by dual promoter-driven reporter systems in bone marrow mesenchymal stem cells

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dc.contributor.authorChoi, Seung-Cheol-
dc.contributor.authorShim, Wan-Joo-
dc.contributor.authorLim, Do-Sun-
dc.date.accessioned2021-09-09T08:57:58Z-
dc.date.available2021-09-09T08:57:58Z-
dc.date.created2021-06-10-
dc.date.issued2008-05-
dc.identifier.issn0141-5492-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/123670-
dc.description.abstractVectors encoding reporter genes driven by cardiac specific myosin light chain- 2v ( MLC- 2v), endothelial cell- specific Flk1 or Tie2 promoters were constructed. The cardiac differentiation- monitoring vector ( pMLC- 2v- DsRed), endothelial cell- specific monitoring vectors ( pFlk1- EGFP, pTie2- EGFP) as well as the dual promoter driven- reporter genes ( pMLC- 2v- DsRed- Flk1- EGFP, pMLC- 2v- DsRed-Tie2- EGFP) were specifically expressed in the Sca-1(+) bone marrow mesenchymal stem cells ( BMMSCs) with cardiomyogenic or endothelial lineage differentiation. The cardiac or endothelial cell- specific promoter- driven reporter vectors provide important tools for the study of stem cell fate and differentiation in vitro and future stem cell therapy for ischemic cardiomyopathy.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectRECEPTOR-2 FLK-1 PROMOTER-
dc.subjectGROWTH-FACTOR-
dc.subjectTRANSGENIC MICE-
dc.subjectIN-VIVO-
dc.subjectEXPRESSION-
dc.subjectFUSION-
dc.subjectCARDIOMYOCYTES-
dc.subjectIDENTIFICATION-
dc.subjectSEQUENCES-
dc.subjectGENE-
dc.titleSpecific monitoring of cardiomyogenic and endothelial differentiation by dual promoter-driven reporter systems in bone marrow mesenchymal stem cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Seung-Cheol-
dc.contributor.affiliatedAuthorShim, Wan-Joo-
dc.contributor.affiliatedAuthorLim, Do-Sun-
dc.identifier.doi10.1007/s10529-007-9631-z-
dc.identifier.scopusid2-s2.0-41549150364-
dc.identifier.wosid000254452400008-
dc.identifier.bibliographicCitationBIOTECHNOLOGY LETTERS, v.30, no.5, pp.835 - 843-
dc.relation.isPartOfBIOTECHNOLOGY LETTERS-
dc.citation.titleBIOTECHNOLOGY LETTERS-
dc.citation.volume30-
dc.citation.number5-
dc.citation.startPage835-
dc.citation.endPage843-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusRECEPTOR-2 FLK-1 PROMOTER-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusTRANSGENIC MICE-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusFUSION-
dc.subject.keywordPlusCARDIOMYOCYTES-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusSEQUENCES-
dc.subject.keywordPlusGENE-
dc.subject.keywordAuthorcardiomyogenic differentiation-
dc.subject.keywordAuthordual promoters-
dc.subject.keywordAuthorendothelial differentiation-
dc.subject.keywordAuthormesenchymal stem cells-
dc.subject.keywordAuthorreporter genes-
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