Natakarn NimsanorIda JørringMikkel A. RasmussenChristian ClausenUlrike A. Mau-HolzmannChristine BusSusanna A. HoffmannThomas GasserTorsten KlubaBjørn HolstBenjamin SchmidBioneer ASUniversität TübingenMahidol UniversityHertie-Institut fur klinische HirnforschungKlinik für Orthopädie und Orthopädische Chirurgie2018-12-112019-03-142018-12-112019-03-142016-11-01Stem Cell Research. Vol.17, No.3 (2016), 550-55218767753187350612-s2.0-85028045546https://repository.li.mahidol.ac.th/handle/20.500.14594/42887© 2016 Michael Boutros, German Cancer Research Center, Heidelberg, Germany Induced pluripotent stem cells (iPSCs) hold great promise to model diseases, where the disease affected cell type is difficult to access. A major obstacle for the development of disease models is the lack of well characterized control iPSCs from old people not affected by such a disease. Furthermore, gene-editing approaches often require iPSCs from healthy donors, where pathogenic mutations can be inserted if patient material is not available. Here, we report the generation of an iPSC line (16423 #6) from a 77-year-old woman, who did not display any disease symptoms at the time, when the skin biopsy was taken.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1016/j.scr.2016.09.019