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key="summary_wrapped">Chondro/osteoblastic and cardiovascular-disease associated genes are modulated in human coronary artery smooth muscle cells that calcify...</item><item key="geo_gse_id">E-GEOD-11917</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">105</item><item key="tags"><item>artery</item><item>coronary artery</item><item>disease</item><item>muscle</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-human-coronary-artery-s</item><item key="geo_id_plat">E-GEOD-11917_A-AFFY-44</item><item key="name">Transcription profiling of human coronary artery smooth muscle treated with vitamin D sterol</item><item key="created">Sep.03, 2014</item><item key="summary">Chondro/osteoblastic and cardiovascular-disease associated genes are modulated in human coronary artery smooth muscle cells that calcify in the presence of phosphate and vitamin D sterols. Looking at the effect of media conditions with and without Vitamin D, paracalcitriol (a vitamin D analog), or R568 (a calcimimetic) vs. dose and time on calcification of human coronary smooth muscle cells. Experiment Overall Design: CASMCs were exposed to differentiation medium [beta glycerophosphate (10 mM), ascorbic acid (50 mg/ml), and dexamethasone (10-9 M) with and without calcitriol or paricalcitol (10-8 M) for 7 days, and total RNA was examined by microarray.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-11917</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-11917/samples/</item></data></biogps>
