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dc.contributor.authorGallagher, Louise
dc.date.accessioned2021-03-08T21:35:30Z
dc.date.available2021-03-08T21:35:30Z
dc.date.issued2020
dc.date.submitted2020en
dc.identifier.citationDing, Y., de la Cruz, B.M., McInerney, V., Lu, Y., Yang, G., Qian, X., Li, W., Krawczyk, J., Howard, L., O'Brien, T., Gallagher, L., Shen, S., Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A), Stem Cell Research, 2020 Dec;49:102101en
dc.identifier.otherY
dc.description.abstractThe induced pluripotent stem cell (iPSC) technology has offered an unprecedented opportunity for disease modelling and drug discovery. Here we used non-integrating Sendai viral method and derived iPSCs from three young healthy Caucasian donors. All iPSCs expressed pluripotency markers highly and could be differentiated into three germ lineages. They possess normal karyotype which was confirmed by whole genome SNP array. The availability of the healthy control iPSCs offers an opportunity for phenotypic comparison and genome editing for a variety of diseases.en
dc.language.isoenen
dc.relation.ispartofseriesStem Cell Research;
dc.relation.ispartofseries49;
dc.relation.ispartofseries102101;
dc.rightsYen
dc.subjectinduced pluripotent stem cell (iPSC)en
dc.subjectdisease modellingen
dc.subjectdrug discoveryen
dc.titleDerivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A)en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lgallagh
dc.identifier.rssinternalid225053
dc.identifier.doihttp://dx.doi.org/10.1016/j.scr.2020.102101
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0001-9462-2836
dc.contributor.sponsorScience Foundation Irelanden
dc.contributor.sponsorGrantNumber13/IA/1787en
dc.identifier.urihttp://hdl.handle.net/2262/95603


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