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A microfluidic array for quantitative analysis of human neural stem cell self-renewal and differentiation in three-dimensional hypoxic microenvironment

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dc.contributor.authorYang, Kisuk-
dc.contributor.authorHan, Sewoon-
dc.contributor.authorShin, Yoojin-
dc.contributor.authorKo, Eunkyung-
dc.contributor.authorKim, Jin-
dc.contributor.authorPark, Kook In-
dc.contributor.authorChung, Seok-
dc.contributor.authorCho, Seung-Woo-
dc.date.accessioned2021-09-05T22:00:14Z-
dc.date.available2021-09-05T22:00:14Z-
dc.date.created2021-06-14-
dc.date.issued2013-09-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102229-
dc.description.abstractWe report a microfluidic array for investigating and quantitatively analyzing human neural stem cell (hNSC) self-renewal and differentiation in an in vivo-like microenvironment. NSC niche conditions, including three-dimensional (3D) extracellular matrices and low oxygen tension, were effectively reconstituted in the microfluidic array in a combinatorial manner. The array device was fabricated to be detachable, rendering it compatible with quantitative real-time polymerase chain reaction for quantifying the effects of the biomimetic conditions on hNSC self-renewal and differentiation. We show that throughput of 3D cell culture and quantitative analysis can be increased. We also show that 3D hypoxic microenvironments maintain hNSC self-renewal capacity and direct neuronal commitment during hNSC differentiation. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.subjectHUMAN NEURODEGENERATIVE DISORDERS-
dc.subjectEXTRACELLULAR-MATRIX-
dc.subjectDOPAMINERGIC DIFFERENTIATION-
dc.subjectVASCULAR NICHE-
dc.subjectPROLIFERATION-
dc.subjectOXYGEN-
dc.subjectCULTURE-
dc.subjectHYDROXYLATION-
dc.subjectNEUROGENESIS-
dc.subjectPLURIPOTENCY-
dc.titleA microfluidic array for quantitative analysis of human neural stem cell self-renewal and differentiation in three-dimensional hypoxic microenvironment-
dc.typeArticle-
dc.contributor.affiliatedAuthorChung, Seok-
dc.identifier.doi10.1016/j.biomaterials.2013.05.067-
dc.identifier.scopusid2-s2.0-84879461661-
dc.identifier.wosid000322049200007-
dc.identifier.bibliographicCitationBIOMATERIALS, v.34, no.28, pp.6607 - 6614-
dc.relation.isPartOfBIOMATERIALS-
dc.citation.titleBIOMATERIALS-
dc.citation.volume34-
dc.citation.number28-
dc.citation.startPage6607-
dc.citation.endPage6614-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusHUMAN NEURODEGENERATIVE DISORDERS-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusDOPAMINERGIC DIFFERENTIATION-
dc.subject.keywordPlusVASCULAR NICHE-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusOXYGEN-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusHYDROXYLATION-
dc.subject.keywordPlusNEUROGENESIS-
dc.subject.keywordPlusPLURIPOTENCY-
dc.subject.keywordAuthorMicrofluidic array-
dc.subject.keywordAuthorNeural stem cells-
dc.subject.keywordAuthorHypoxia-
dc.subject.keywordAuthorSelf-renewal-
dc.subject.keywordAuthorDifferentiation-
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