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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM1105583"><item key="TREATMENT">untreated</item></item></item><item><item key="GSM1105584"><item key="TREATMENT">treated with TGF-beta2</item></item></item><item><item key="GSM1105585"><item key="TREATMENT">treated with SB431542 and TGF-beta2</item></item></item><item><item key="GSM1105586"><item key="TREATMENT">treated with 5Z-7-Oxozeaenol and TGF-beta2</item></item></item></item><item key="id">7219</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">TGF-beta signaling in neural crest cells is required for normal craniofacial development. This signaling can be transduced via TGF-beta...</item><item key="geo_gse_id">E-GEOD-45491</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">4</item><item key="tags"><item>cell</item><item>crest</item><item>mesenchymal cell</item><item>neural crest</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-palatal-mesenchymal-cells</item><item key="geo_id_plat">E-GEOD-45491_A-AFFY-45</item><item key="name">Expression profiling in palatal mesenchymal cells stimulated with TGF-beta2 in the presence and absence of TGFbRI and Tak1 kinase inhibitors</item><item key="created">Nov.12, 2014</item><item key="summary">TGF-beta signaling in neural crest cells is required for normal craniofacial development. This signaling can be transduced via TGF-beta type I receptors (TGFbRI) using Smad-dependent or Smad independent signaling pathways. We used microarrays to identify TGF-beta-responsive genes that are dependent either on TGFbRI kinase, Tak1 kinase or both. Primary palatal mesenchymal cell cultures were established. Cultured cells were stimulated with TGF-beta2 in the presence or absence of TGFbRI kinase and Tak1 kinase inhibitors. Unstimulated cells were used as controls. Total RNAs were isolated and hybridized on Affymetrix microarrays.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-45491</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-45491/samples/</item></data></biogps>
