{"owner": "ArrayExpress Uploader", "pop_total": 0, "species": "mouse", "factors": [{"GSE13869GSM349023": {}}, {"GSE13869GSM349024": {}}, {"GSE13869GSM349025": {}}, {"GSE13869GSM349026": {}}, {"GSE13869GSM349027": {}}, {"GSE13869GSM349028": {}}, {"GSE13869GSM349029": {}}, {"GSE13869GSM349030": {}}], "id": 5571, "ownerprofile_id": "arrayexpress_sid", "platform": 6, "summary_wrapped": "Rod-derived Cone Viability Factor (RdCVF, alias nxnl1) is a retina-specific protein identified for its therapeutic potential in...", "geo_gse_id": "E-GEOD-13869", "owner_profile": "/profile/8773/arrayexpressuploader", "factor_count": 0, "sample_count": 8, "tags": ["cone", "protein", "retina", "retinal degeneration"], "lastmodified": "Dec.12, 2014", "is_default": false, "geo_id_plat": "E-GEOD-13869_A-AFFY-45", "slug": "transcription-profiling-of-mouse-nxnl1-retina", "geo_gds_id": "", "name": "Transcription profiling of mouse  Nxnl1-/-  retina", "created": "Nov.10, 2014", "summary": "Rod-derived Cone Viability Factor (RdCVF, alias nxnl1) is a retina-specific protein identified for its therapeutic potential in supporting cone survival during retinal degeneration. A nxnl1 knockout mouse model was created and the transcriptome used to demonstrate that the retina is compromised by the absence of nxnl1. Experiment Overall Design: In total 9 samples were analyzed, they represent three different genotypes (wt/wt, ko/wt, ko/ko) that were tested in triplicate each.", "source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-13869", "sample_source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-13869/samples/"}