{"owner": "ArrayExpress Uploader", "pop_total": 0, "species": "human", "factors": [{"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764189": {"DISEASE STATUS": "affected"}}, {"GSM764196": {"DISEASE STATUS": "unaffected"}}, {"GSM764196": {"DISEASE STATUS": "unaffected"}}, {"GSM764196": {"DISEASE STATUS": "unaffected"}}], "id": 4180, "ownerprofile_id": "arrayexpress_sid", "platform": 4, "summary_wrapped": "Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is caused by mutations in the Valosin...", "geo_gse_id": "E-GEOD-30806", "owner_profile": "/profile/8773/arrayexpressuploader", "factor_count": 1, "sample_count": 10, "tags": ["body", "bone", "chromosome", "dementia", "disease", "frontotemporal dementia", "ibmpfd", "muscle", "myopathy", "paget disease of bone", "protein"], "lastmodified": "Dec.12, 2014", "is_default": false, "geo_gds_id": "", "slug": "expression-profiling-in-vcp-associated-myopathy", "geo_id_plat": "E-GEOD-30806_A-AFFY-44", "name": "Expression profiling in VCP-associated myopathy", "created": "Sep.16, 2014", "summary": "Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is caused by mutations in the Valosin Containing Protein (VCP) gene on chromosome 9p12-13. To elucidate affected signaling transduction axes in IBMPFD, we determined expression profiles using microarray technology in quadriceps muscle from patients and unaffected relatives. Muscle from 10 individuals  (7 affected, 3 unaffected first degree relatives) was obtained after informed consent for the muscle biopsy was obtained.", "source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30806", "sample_source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30806/samples/"}