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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">mouse</item><item key="factors"><item><item key="GSE15871GSM398437"/></item><item><item key="GSE15871GSM398438"/></item><item><item key="GSE15871GSM398439"/></item><item><item key="GSE15871GSM398440"/></item><item><item key="GSE15871GSM398441"/></item><item><item key="GSE15871GSM398442"/></item><item><item key="GSE15871GSM398443"/></item><item><item key="GSE15871GSM398444"/></item><item><item key="GSE15871GSM398445"/></item><item><item key="GSE15871GSM398446"/></item><item><item key="GSE15871GSM398447"/></item><item><item key="GSE15871GSM398448"/></item><item><item key="GSE15871GSM398449"/></item><item><item key="GSE15871GSM398450"/></item><item><item key="GSE15871GSM398451"/></item><item><item key="GSE15871GSM398452"/></item><item><item key="GSE15871GSM398453"/></item><item><item key="GSE15871GSM398454"/></item></item><item key="id">5684</item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">The Nuclear Factor I C (NFI-C) transcription factor has been implicated in TGF-&#946; signaling, extracellular matrix deposition and skin...</item><item key="pubmed_id">19752192</item><item key="geo_gse_id">E-GEOD-15871</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">18</item><item key="tags"><item>fibroblast</item><item>skin</item><item>skin appendage</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-15871_A-AFFY-45</item><item key="slug">transcription-profiling-of-mouse-nfi-c-knock-out-e</item><item key="geo_gds_id"/><item key="name">Transcription profiling of mouse NFI-C knock out embryonic fibroblasts</item><item key="created">Nov.11, 2014</item><item key="summary">The Nuclear Factor I C (NFI-C) transcription factor has been implicated in TGF-&#946; signaling, extracellular matrix deposition and skin appendage pathologies. We performed a global gene expression analysis in NFI-C-/- and wild-type embryonic primary murine fibroblasts. This indicated that NFI-C acts mostly to repress gene expression in response to TGF-&#946;1. Misregulated genes featured a prominent over-representation of regulators of connective tissue inflammation and repair. Experiment Overall Design: mRNAs were isolated from embryonic fibroblasts obtained from 3 wild-type and 3 NFI-C knock-out mice, and their levels were probed using microarrays. Prior to RNA extraction, fibroblast cultures were treated or not with TGF-&#946;1 for 1 hour to examine the immediate response to the growth factor, or treated for 10 hours to assess the delayed response.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-15871</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-15871/samples/</item></data></biogps>
