Generation of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation

Cited 5 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorS Y Lee-
dc.contributor.authorS Jeong-
dc.contributor.authorJanghwan Kim-
dc.contributor.authorS K Chung-
dc.date.accessioned2018-07-19T16:30:36Z-
dc.date.available2018-07-19T16:30:36Z-
dc.date.issued2018-
dc.identifier.issn1873-5061-
dc.identifier.uri10.1016/j.scr.2018.06.002ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17921-
dc.description.abstractParkinson'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.publisherElsevier-
dc.titleGeneration of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation-
dc.title.alternativeGeneration of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation-
dc.typeArticle-
dc.citation.titleStem Cell Research-
dc.citation.number0-
dc.citation.endPage149-
dc.citation.startPage145-
dc.citation.volume30-
dc.contributor.affiliatedAuthorJanghwan Kim-
dc.contributor.alternativeName이서영-
dc.contributor.alternativeName정상균-
dc.contributor.alternativeName김장환-
dc.contributor.alternativeName정선구-
dc.identifier.bibliographicCitationStem Cell Research, vol. 30, pp. 145-149-
dc.identifier.doi10.1016/j.scr.2018.06.002-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.