{"owner": "ArrayExpress Uploader", "ownerprofile_id": "arrayexpress_sid", "species": "mouse", "factors": [{"GSM1177838": {"T-CELL SUBSET": "Th0 cells"}}, {"GSM1177839": {"T-CELL SUBSET": "Th17 cells"}}, {"GSM1177840": {"T-CELL SUBSET": "exFoxp3Th17 cells"}}, {"GSM117784": {"T-CELL SUBSET": "Treg cells"}}], "id": 7359, "pop_total": 0, "platform": 6, "summary_wrapped": "Foxp3 is indispensable for Treg suppressive function, but the stability of Foxp3 has been controversial. In autoimmune arthritis, Th17...", "geo_gse_id": "E-GEOD-48428", "owner_profile": "/profile/8773/arrayexpressuploader", "factor_count": 1, "sample_count": 4, "tags": ["arthritis", "cell"], "lastmodified": "Dec.12, 2014", "is_default": false, "geo_id_plat": "E-GEOD-48428_A-AFFY-45", "slug": "expression-data-from-th17-cells-of-different-origi", "geo_gds_id": "", "name": "Expression data from Th17 cells of different origins", "created": "Nov.12, 2014", "summary": "Foxp3 is indispensable for Treg suppressive function, but the stability of Foxp3 has been controversial. In autoimmune arthritis, Th17 cells play a critically important pathological role, but the origin of Th17 cells remains unknown We used microarrays to detail the global programme of gene expression of Th17 cells originated from Foxp3+T cells compared to conventional naive CD4+T cells derived Th17 cells. We also take samples of Treg cells and Th0 cells for the experimetnatl control. Each T cell subset after the culture was subjected to RNA extraction and hybridization on Affymetrix microarrays.", "source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-48428", "sample_source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-48428/samples/"}