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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">human</item><item key="factors"><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713542"><item key="CELL LINE">IMR-90</item><item key="ORGANISM PART">Lung Fibroblast</item></item></item><item><item key="GSM713549"><item key="CELL LINE">H1</item><item key="ORGANISM PART">blastocyst</item></item></item><item><item key="GSM713554"><item key="CELL LINE">HUES9</item><item key="ORGANISM PART">blastocyst</item></item></item><item><item key="GSM713560"><item key="CELL LINE">FTC1</item><item key="ORGANISM PART">Foreskin Fibroblast</item></item></item><item><item key="GSM713560"><item key="CELL LINE">FTC1</item><item key="ORGANISM PART">Foreskin Fibroblast</item></item></item><item><item key="GSM713560"><item key="CELL LINE">FTC1</item><item key="ORGANISM PART">Foreskin Fibroblast</item></item></item><item><item key="GSM713560"><item key="CELL LINE">FTC1</item><item key="ORGANISM PART">Foreskin Fibroblast</item></item></item><item><item key="GSM713549"><item key="CELL LINE">H1</item><item key="ORGANISM PART">blastocyst</item></item></item><item><item key="GSM713554"><item key="CELL LINE">HUES9</item><item key="ORGANISM PART">blastocyst</item></item></item></item><item key="id">4065</item><item key="pop_total">0</item><item key="platform">4</item><item key="summary_wrapped">The undifferentiated state of pluripotent stem cells depends heavily on the culture conditions.  We show that a unique combination of...</item><item key="pubmed_id">22355727</item><item key="geo_gse_id">E-GEOD-28815</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">14</item><item key="tags"/><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-comparison-between-smc4-and-conventiona</item><item key="geo_id_plat">E-GEOD-28815_A-AFFY-44</item><item key="name">Expression comparison between SMC4 and conventional cultures</item><item key="created">Sep.16, 2014</item><item key="summary">The undifferentiated state of pluripotent stem cells depends heavily on the culture conditions.  We show that a unique combination of small molecules, SMC4, added to culture conditions converts primed pluripotent stem cells to a more na&#239;ve state.  By conducting Affymetix analysis we show of majority of lineage markers are repressed in SMC4 culture. Human embryonic stem cells were compared to human induced pluripotent stem cells cultured in either primed or na&#239;ve conditions.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-28815</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-28815/samples/</item></data></biogps>
