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DC FieldValueLanguage
dc.contributor.author박장환-
dc.date.accessioned2019-11-27T19:36:40Z-
dc.date.available2019-11-27T19:36:40Z-
dc.date.issued2017-07-
dc.identifier.citationBIOMOLECULES & THERAPEUTICS, v. 25, no. 4, page. 362-366en_US
dc.identifier.issn1976-9148-
dc.identifier.issn2005-4483-
dc.identifier.urihttp://www.biomolther.org/journal/view.html?volume=25&number=4&spage=362&year=2017-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/114949-
dc.description.abstractDirect conversion by trans-differentiation is of growing interest in cell therapy for incurable diseases. The efficiency of cell reprogramming and functionality of converted cells are important considerations in cell transplantation therapy. Here, we compared two representative protocols for the generation of Induced-oligodendrocyte progenitor cells (iOPCs) from mouse and rat fibroblasts. Then, we showed that induction of Nkx6.2, Olig2, and Sox10 (NOS) was more effective in mouse fibroblasts and that induction of Olig2, Sox10, and Zfp536 (OSZ) was more effective at reprogramming iOPCs from rat fibroblasts. However, OSZ-iOPCs did not show greater proliferation than NOS-induced cells. Because the efficiency of iOPCs generation appears to differ between cell species depending on transcription factors and culture conditions, it is important to select appropriate methods for efficient reprogramming.en_US
dc.description.sponsorshipThis research was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HI16C1013).en_US
dc.language.isoen_USen_US
dc.publisherKOREAN SOC APPLIED PHARMACOLOGYen_US
dc.subjectDirect conversionen_US
dc.subjectOligodendrocyteen_US
dc.subjectiOPCen_US
dc.subjectEfficiencyen_US
dc.titleComparison of Reprogramming Methods for Generation of Induced-Oligodendrocyte Precursor Cellsen_US
dc.typeArticleen_US
dc.relation.no4-
dc.relation.volume25-
dc.identifier.doi10.4062/biomolther.2017.066-
dc.relation.page362-366-
dc.relation.journalBIOMOLECULES & THERAPEUTICS-
dc.contributor.googleauthorLee, Eun-Hye-
dc.contributor.googleauthorPark, Chang-Hwan-
dc.relation.code2017009252-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidchshpark-


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