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dc.contributor.advisor Kim, Jeong Beom -
dc.contributor.author Jeong, Yujin -
dc.date.accessioned 2024-01-25T14:13:27Z -
dc.date.available 2024-01-25T14:13:27Z -
dc.date.issued 2017-08 -
dc.description.abstract Although long non-coding RNAs (lncRNAs) have emerged as novel regulator of cell fate and gene expression, the regulation of vascular specific transcription factor by lncRNA in generation of induced endothelial cells (iEndo) has not been studied yet. In this study, ETS variant 2 (ETV2) converts human fibroblasts into iEndo, and smooth muscle and endothelial cell enriched migration/differentiationassociated long non-coding RNA (SENCR) was identified as a regulator of ETV2. iEndo showed similar morphology, endothelial cell markers, and tubular structure formation compared to human umbilical vein endothelial cell (HUVEC). Furthermore, over-expression of SENCR increased ETV2 gene and protein expression by enhancing ETV2 promoter activity through recruitment of PSPC1. This is the first study demonstrates the role of SENCR contributed to ETV2 activation in generation of iEndo. -
dc.description.degree Master -
dc.description Departmentof Biological Sciences -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/72220 -
dc.identifier.uri http://unist.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002377292 -
dc.language eng -
dc.publisher Ulsan National Institute of Science and Technology (UNIST) -
dc.rights.embargoReleaseDate 9999-12-31 -
dc.rights.embargoReleaseTerms 9999-12-31 -
dc.title Long non-coding RNA SENCR is a positive regulator of ETV2 -
dc.type Thesis -

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