ArrayExpress Uploader0humaninduced pluripotent stem cell line 1inemononuclearbone marrowinduced pluripotent stem cell line1Lmononuclearbone marrowinduced pluripotent stem cell line 1Mmononuclearbone marrowinduced pluripotent stem cell line 9mononuclearbone marrow mononuclearbone marrowinduced pluripotent stem cell line 6mononuclearumbilical cordinduced pluripotent stem cell line T4mononuclearumbilical cordinduced pluripotent stem cell line 15mononuclearbone marrowH1embryonic stem cell induced pluripotent stem cell line DF19-9fibroblastnot specifiedinduced pluripotent stem cell line DF19-9-11fibroblastnot specifiedinduced pluripotent stem cell line DF19-9-7Tfibroblastnot specifiedinduced pluripotent stem cell line DF6-9fibroblastnot specifiedinduced pluripotent stem cell line DF6-9-9Tfibroblastnot specified fibroblastforeskinH13Bembryonic stem cell H13Aembryonic stem cell H7embryonic stem cell H9embryonic stem cell 3929arrayexpress_sid4global gene expression were compared among human blood iPSC, human fibroblas iPSC, human embryonic stem cells, human bone marrow MNC and...E-GEOD-26672/profile/8773/arrayexpressuploader319bonebone marrowfibroblastDec.12, 2014Falsetranscription-profiling-of-transgene-free-inducedE-GEOD-26672_A-AFFY-44Transcription profiling of Transgene-Free Induced Pluripotent Stem Cells from Normal and Neoplastic Bone Marrow and Cord Blood Mononuclear Cells .Sep.15, 2014global gene expression were compared among human blood iPSC, human fibroblas iPSC, human embryonic stem cells, human bone marrow MNC and human forskin fibroblast Reprogramming blood cells to induced pluripotent stem cells (iPSCs) provides a novel tool for modeling blood diseases in vitro. we demonstrated that iPSCs free of transgene and vector sequences could be efficiently generated from human bone marrow and cord blood mononuclear cells using non-integrating episomal vectors. The reprogramming described here is up to 100 times more efficient, occurs 1 to 3 weeks faster as compared to the reprogramming of fibroblasts, and does not require isolation of progenitors or multiple rounds of transfection. This approach provides an opportunity to explore banked normal and diseased cord blood and bone marrow samples without the limitations associated with virus-based methods. Compare the global gene expression of iPSs from different sources, ESCs and Somatic cellshttp://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-26672http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-26672/samples/