A homozygous Keap1-knockout human embryonic stem cell line generated using CRISPR/Cas9 mediates gene targeting
DC Field | Value | Language |
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dc.contributor.author | Kim, SJ | - |
dc.contributor.author | Omer Habib | - |
dc.contributor.author | Jin-Soo Kim | - |
dc.contributor.author | Han, HW | - |
dc.contributor.author | Koo, SK | - |
dc.contributor.author | Kim, JH | - |
dc.date.available | 2019-02-25T05:37:17Z | - |
dc.date.created | 2017-04-24 | - |
dc.date.issued | 2017-03 | - |
dc.identifier.issn | 1873-5061 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/5617 | - |
dc.description.abstract | Kelch-like ECH-associated protein 1 (keap1) is a cysteine-rich protein that interacts with transcription factor Nrf2 in a redox-sensitive manner, leading to the degradation of Nrf2 (Kim et al., 2014a). Disruption of Keap1 results in the induction of Nrf2-related signaling pathways involving the expression of a set of anti-oxidant and anti-inflammatory genes. We generated biallelic mutants of the Keap1 gene using a CRISPR-Cas9 genome editing method in the H9 human embryonic stem cell (hESC). The Keap1 homozygous-knockout H9 cell line retained normal morphology, gene expression, and in vivo differentiation potential. (C) 2016 The Author(s). Published by Elsevier B.V | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | ELSEVIER SCIENCE BV | - |
dc.title | A homozygous Keap1-knockout human embryonic stem cell line generated using CRISPR/Cas9 mediates gene targeting | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000397450700012 | - |
dc.identifier.scopusid | 2-s2.0-85020318911 | - |
dc.identifier.rimsid | 59208 | - |
dc.contributor.affiliatedAuthor | Omer Habib | - |
dc.contributor.affiliatedAuthor | Jin-Soo Kim | - |
dc.identifier.doi | 10.1016/j.scr.2016.12.028 | - |
dc.identifier.bibliographicCitation | STEM CELL RESEARCH, v.19, pp.52 - 54 | - |
dc.citation.title | STEM CELL RESEARCH | - |
dc.citation.volume | 19 | - |
dc.citation.startPage | 52 | - |
dc.citation.endPage | 54 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |