<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">3211</item><item key="factors"><item><item key="GSM380009 1"/></item><item><item key="GSM380010 1"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Oculo-facio-cardio-dental syndrome (OFCD) is a rare genetic disorder characterized by teeth with extremely long roots (radiculomegaly),...</item><item key="pubmed_id">19578371</item><item key="geo_gse_id">E-GEOD-15214</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>apical</item><item>eye</item><item>genetic disorder</item><item>syndrome</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">bcor-regulated-genes-in-human-oculo-facio-cardio-d</item><item key="geo_id_plat">E-GEOD-15214_A-AFFY-44</item><item key="name">BCOR-regulated genes in human oculo-facio-cardio-dental syndrome</item><item key="created">Sep.12, 2014</item><item key="summary">Oculo-facio-cardio-dental syndrome (OFCD) is a rare genetic disorder characterized by teeth with extremely long roots (radiculomegaly), and craniofacial, eye and cardiac abnormalities. The mutation of the transcriptional co-repressor BCOR has been identified as being responsible for oculo-facio-cardio-dental (OFCD) syndrome. Mesenchymal stem cells (MSCs) is isolated from the root apical papilla of an OFCD patient. Gene expression profiling is performed and compared between mutant MSCs and wild type MSCs. Total RNA were extracted from normal MSCs (MSCWT) and mutant MSCs (MSCO).</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-15214</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-15214/samples/</item></data></biogps>
