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Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12322
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dc.contributor.authorTongkobpetch S.
dc.contributor.authorRungsiwiwut R.
dc.contributor.authorPruksananonda K.
dc.contributor.authorSuphapeetiporn K.
dc.contributor.authorShotelersuk V.
dc.date.accessioned2021-04-05T03:02:47Z-
dc.date.available2021-04-05T03:02:47Z-
dc.date.issued2019
dc.identifier.issn18735061
dc.identifier.other2-s2.0-85069590379
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12322-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85069590379&doi=10.1016%2fj.scr.2019.101493&partnerID=40&md5=4e1ce5eee7a33b41e23cb8f86cf3a22a
dc.description.abstractTwo clones of human induced pluripotent stem cells (iPSCs) were generated from dermal fibroblasts isolated from a one-year-old Thai patient with X-linked osteogenesis imperfecta. The patient harbored a mutation, p.N459S, in the MBTPS2 gene. The cells were reprogrammed using an integration-free Sendai virus containing KLF4, c-MYC, OCT4 and SOX2. Both of the established iPSC lines (MDCUi001-A and MDCUi001-B) maintained normal karyotype, expressed pluripotent markers and differentiated into all three germ layers. © 2019
dc.subjectafp1 protein
dc.subjectalpha smooth muscle actin
dc.subjectbeta tubulin
dc.subjectcell marker
dc.subjectgenomic DNA
dc.subjectglyceraldehyde 3 phosphate dehydrogenase
dc.subjectkruppel like factor 4
dc.subjectmembrane bound transcription factor peptidase site 2
dc.subjectMyc protein
dc.subjectoctamer transcription factor 4
dc.subjectpeptidase
dc.subjectrex1 protein
dc.subjecttra 1 60 protein
dc.subjecttra 1 81 protein
dc.subjecttranscription factor
dc.subjecttranscription factor NANOG
dc.subjecttranscription factor Sox2
dc.subjectunclassified drug
dc.subjectkruppel like factor
dc.subjectkruppel like factor 4
dc.subjectMyc protein
dc.subjectMYC protein, human
dc.subjectSOX2 protein, human
dc.subjecttranscription factor Sox
dc.subjectArticle
dc.subjectcell clone
dc.subjectcell differentiation
dc.subjectcell reprogramming technique
dc.subjectchild
dc.subjectcontrolled study
dc.subjectectoderm
dc.subjectembryoid body
dc.subjectendoderm
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectinduced pluripotent stem cell
dc.subjectkaryotype
dc.subjectmale
dc.subjectmdcui001 a cell line
dc.subjectmdcui001 b cell line
dc.subjectmesoderm
dc.subjectnonhuman
dc.subjectnuclear reprogramming
dc.subjectosteogenesis imperfecta
dc.subjectpluripotent stem cell line
dc.subjectpoint mutation
dc.subjectpreschool child
dc.subjectpriority journal
dc.subjectSendai virus
dc.subjectshort tandem repeat
dc.subjectskin fibroblast
dc.subjectThai (people)
dc.subjectcell line
dc.subjectcytology
dc.subjectfibroblast
dc.subjectgenetics
dc.subjectinduced pluripotent stem cell
dc.subjectmetabolism
dc.subjectosteogenesis imperfecta
dc.subjectphysiology
dc.subjectSendai virus
dc.subjectThailand
dc.subjectCell Differentiation
dc.subjectCell Line
dc.subjectFibroblasts
dc.subjectHumans
dc.subjectInduced Pluripotent Stem Cells
dc.subjectKaryotype
dc.subjectKruppel-Like Transcription Factors
dc.subjectMale
dc.subjectOsteogenesis Imperfecta
dc.subjectProto-Oncogene Proteins c-myc
dc.subjectSendai virus
dc.subjectSOXB1 Transcription Factors
dc.subjectThailand
dc.titleGeneration of two human iPSC lines (MDCUi001-A and MDCUi001-B) from dermal fibroblasts of a Thai patient with X-linked osteogenesis imperfecta using integration-free Sendai virus
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationStem Cell Research. Vol 39, (2019)
dc.identifier.doi10.1016/j.scr.2019.101493
Appears in Collections:Scopus 1983-2021

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