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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764189"><item key="DISEASE STATUS">affected</item></item></item><item><item key="GSM764196"><item key="DISEASE STATUS">unaffected</item></item></item><item><item key="GSM764196"><item key="DISEASE STATUS">unaffected</item></item></item><item><item key="GSM764196"><item key="DISEASE STATUS">unaffected</item></item></item></item><item key="id">4180</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is caused by mutations in the Valosin...</item><item key="geo_gse_id">E-GEOD-30806</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">10</item><item key="tags"><item>body</item><item>bone</item><item>chromosome</item><item>dementia</item><item>disease</item><item>frontotemporal dementia</item><item>ibmpfd</item><item>muscle</item><item>myopathy</item><item>paget disease of bone</item><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-profiling-in-vcp-associated-myopathy</item><item key="geo_id_plat">E-GEOD-30806_A-AFFY-44</item><item key="name">Expression profiling in VCP-associated myopathy</item><item key="created">Sep.16, 2014</item><item key="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.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30806</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30806/samples/</item></data></biogps>
