{"owner": "ArrayExpress Uploader", "ownerprofile_id": "arrayexpress_sid", "id": 6788, "factors": [{"GSE3583GSM82441": {"DISEASESTATE": "normal", "GENOTYPE": "wild_type", "COMPOUND": "3-nitropropionic acid"}}, {"GSE3583GSM82441": {"DISEASESTATE": "normal", "GENOTYPE": "wild_type", "COMPOUND": "3-nitropropionic acid"}}, {"GSE3583GSM82441": {"DISEASESTATE": "normal", "GENOTYPE": "wild_type", "COMPOUND": "3-nitropropionic acid"}}, {"GSE3583GSM82444": {"DISEASESTATE": "3-NP-induced neurodegeneration model of Huntingtons disease", "GENOTYPE": "wild_type", "COMPOUND": "none"}}, {"GSE3583GSM82444": {"DISEASESTATE": "3-NP-induced neurodegeneration model of Huntingtons disease", "GENOTYPE": "wild_type", "COMPOUND": "none"}}, {"GSE3583GSM82444": {"DISEASESTATE": "3-NP-induced neurodegeneration model of Huntingtons disease", "GENOTYPE": "wild_type", "COMPOUND": "none"}}, {"GSE3583GSM82447": {"DISEASESTATE": "mouse model of Huntingtons disease", "GENOTYPE": "huntingtin mutant", "COMPOUND": "none"}}, {"GSE3583GSM82447": {"DISEASESTATE": "mouse model of Huntingtons disease", "GENOTYPE": "huntingtin mutant", "COMPOUND": "none"}}, {"GSE3583GSM82447": {"DISEASESTATE": "mouse model of Huntingtons disease", "GENOTYPE": "huntingtin mutant", "COMPOUND": "none"}}], "pop_total": 0, "platform": 6, "summary_wrapped": "Affymetrix MG430 2.0 expression levels of wild-type (STHdhQ7/Q7), 3NP-treated wild-type (STHdhQ7/Q7NP), and mutant (STHdhQ111/Q111)...", "pubmed_id": 17708681, "owner_profile": "/profile/8773/arrayexpressuploader", "factor_count": 3, "sample_count": 9, "tags": ["disease"], "lastmodified": "Dec.12, 2014", "is_default": false, "geo_id_plat": "E-GEOD-3583_A-AFFY-45", "slug": "transcription-profiling-of-two-different-mouse-mod", "source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-3583", "geo_gds_id": "", "name": "Transcription profiling of two different mouse models of Huntington's disease - changes caused by Hdh CAG mutation or 3-nitropropionic acid in striatal cells", "created": "Nov.12, 2014", "summary": "Affymetrix MG430 2.0 expression levels of wild-type (STHdhQ7/Q7), 3NP-treated wild-type (STHdhQ7/Q7NP), and mutant (STHdhQ111/Q111) striatal cells Experiment Overall Design: Investigation of HD disease mechanism by gene expression profiling of two HD model systems", "geo_gse_id": "E-GEOD-3583", "species": "mouse", "sample_source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-3583/samples/"}