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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">3750</item><item key="factors"><item><item key="GSM568505"><item key="TREATMENT">shControl</item></item></item><item><item key="GSM568505"><item key="TREATMENT">shControl</item></item></item><item><item key="GSM568505"><item key="TREATMENT">shControl</item></item></item><item><item key="GSM568508"><item key="TREATMENT">shBAP1 #1</item></item></item><item><item key="GSM568508"><item key="TREATMENT">shBAP1 #1</item></item></item><item><item key="GSM568508"><item key="TREATMENT">shBAP1 #1</item></item></item><item><item key="GSM5685"><item key="TREATMENT">shBAP1 #2</item></item></item><item><item key="GSM5685"><item key="TREATMENT">shBAP1 #2</item></item></item><item><item key="GSM5685"><item key="TREATMENT">shBAP1 #2</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">The deubiquitinase BAP1 is a candidate tumor suppressor regulating cell proliferation in human and is required for development in...</item><item key="pubmed_id">20805357</item><item key="geo_gse_id">E-GEOD-23035</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">9</item><item key="tags"><item>cell</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-data-from-bap1-depleted-cells</item><item key="geo_id_plat">E-GEOD-23035_A-AFFY-44</item><item key="name">Expression data from BAP1 depleted cells</item><item key="created">Sep.15, 2014</item><item key="summary">The deubiquitinase BAP1 is a candidate tumor suppressor regulating cell proliferation in human and is required for development in Drosophila. BAP1 is assembled into high molecular weight transcriptional multi-protein complexes. In order to identify potential BAP1 target genes, global mRNA expression profiling using microarrays was conducted. U2OS cells, transfected with a non-target control shRNA or shRNAs targeting BAP1, were selected with puromycin containing medium and then synchronized at the G1/S border to allow comparative analysis of gene expression.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23035</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23035/samples/</item></data></biogps>
