<?xml version="1.0" encoding="ASCII"?>
<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="GSE981GSM15501"/></item><item><item key="GSE981GSM15500"/></item></item><item key="id">1567</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">3</item><item key="summary_wrapped">Primary lung fibroblasts were grown to confluence in DMEM 10% FBS, serum starved in DMEM 0.5% FBS for 18 hours.  Cells were then treated...</item><item key="geo_gse_id">E-GEOD-981</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">2</item><item key="tags"><item>lung</item><item>serum</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-human-endothelin-treate</item><item key="geo_id_plat">E-GEOD-981_A-AFFY-33</item><item key="name">Transcription profiling of human endothelin treated lung fibroblasts</item><item key="created">Jun.19, 2014</item><item key="summary">Primary lung fibroblasts were grown to confluence in DMEM 10% FBS, serum starved in DMEM 0.5% FBS for 18 hours.  Cells were then treated in the presence or absence of 100 nM ET-1 in the same medium for an additional 4 hours.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-981</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-981/samples/</item></data></biogps>
