{"accessLevel": "public", "bureauCode": ["020:00"], "contactPoint": {"fn": "Jon Corton", "hasEmail": "mailto:corton.chris@epa.gov"}, "description": "Gene Expression Omnibus numbers only. \n\nThis dataset is associated with the following publication:\nMesnage, R., A. Phedonos, M. Arno, S. Balu, C. Corton, and M. Antoniou. Transcriptome profiling reveals bisphenol A alternatives activate estrogen receptor alpha in human breast cancer cells.   TOXICOLOGICAL SCIENCES. Society of Toxicology,    158(2): 431-443, (2017).", "distribution": [{"downloadURL": "https://pasteur.epa.gov/uploads/10.23719/1376229/Data%20submission%20for%20A-6wwx.xlsx", "mediaType": "application/vnd.openxmlformats-officedocument.spreadsheetml.sheet", "title": "Data submission for A-6wwx.xlsx"}], "identifier": "https://doi.org/10.23719/1376229", "keyword": ["MCF-7 cell line", "bisphenol A alternatives", "endocrine disruption", "estrogen receptor", "human breast cancer"], "license": "https://pasteur.epa.gov/license/sciencehub-license.html", "modified": "2017-03-01", "programCode": ["020:000"], "publisher": {"name": "U.S. EPA Office of Research and Development (ORD)", "subOrganizationOf": {"name": "U.S. Environmental Protection Agency", "subOrganizationOf": {"name": "U.S. Government"}}}, "references": ["https://doi.org/10.1093/toxsci/kfx101"], "rights": null, "title": "Datasets used in ORD-018902: Bisphenol A alternatives can effectively substitute for estradiol "}