DC Field | Value | Language |
---|---|---|
dc.contributor.author | S Y Lee | - |
dc.contributor.author | S Jeong | - |
dc.contributor.author | Janghwan Kim | - |
dc.contributor.author | S K Chung | - |
dc.date.accessioned | 2018-07-19T16:30:36Z | - |
dc.date.available | 2018-07-19T16:30:36Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1873-5061 | - |
dc.identifier.uri | 10.1016/j.scr.2018.06.002 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/17921 | - |
dc.description.abstract | Parkinson's disease (PD) is the second most common age-related neurodegenerative disorder. PD can result from a mutation of alpha-synuclein (α-SNCA), such as α-SNCA A53T. Using episomal vectors, induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts with the α-SNCA A53T mutation. A huge bacterial artificial chromosome (BAC) harboring the normal α-SNCA gene successfully corrected the α-SNCA A53T-mutant iPSCs. Melting curve analysis for allelic composition indicated that the BAC DNA was precisely targeted to the α-SNCA A53T mutation allele, without random integration. The corrected PD-iPSCs displayed the normal karyotype and pluripotency, with the capability to differentiate to any cell type | - |
dc.publisher | Elsevier | - |
dc.title | Generation of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation | - |
dc.title.alternative | Generation of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation | - |
dc.type | Article | - |
dc.citation.title | Stem Cell Research | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 149 | - |
dc.citation.startPage | 145 | - |
dc.citation.volume | 30 | - |
dc.contributor.affiliatedAuthor | Janghwan Kim | - |
dc.contributor.alternativeName | 이서영 | - |
dc.contributor.alternativeName | 정상균 | - |
dc.contributor.alternativeName | 김장환 | - |
dc.contributor.alternativeName | 정선구 | - |
dc.identifier.bibliographicCitation | Stem Cell Research, vol. 30, pp. 145-149 | - |
dc.identifier.doi | 10.1016/j.scr.2018.06.002 | - |
dc.description.journalClass | Y | - |
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