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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">6365</item><item key="factors"><item><item key="GSM67704"><item key="TREATMENT">control</item></item></item><item><item key="GSM67704"><item key="TREATMENT">control</item></item></item><item><item key="GSM677043"><item key="TREATMENT">dorsomorphin</item></item></item><item><item key="GSM677043"><item key="TREATMENT">dorsomorphin</item></item></item><item><item key="GSM677045"><item key="TREATMENT">stimulated</item></item></item><item><item key="GSM677045"><item key="TREATMENT">stimulated</item></item></item><item><item key="GSM677047"><item key="TREATMENT">stimulated and dorsomorphin</item></item></item><item><item key="GSM677047"><item key="TREATMENT">stimulated and dorsomorphin</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Dorsomorphin is a small molecule inhibitor of type I bone morphogenic protein receptors (BMPRs). We have found that dorsomorphin affects...</item><item key="pubmed_id">22144105</item><item key="geo_gse_id">E-GEOD-27378</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">8</item><item key="tags"><item>bone</item><item>cell</item><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">differential-effects-of-inhibition-of-bone-morphog</item><item key="geo_id_plat">E-GEOD-27378_A-AFFY-45</item><item key="name">Differential effects of inhibition of bone morphogenic protein (BMP) signalling on T-cell activation and differentiation</item><item key="created">Nov.11, 2014</item><item key="summary">Dorsomorphin is a small molecule inhibitor of type I bone morphogenic protein receptors (BMPRs). We have found that dorsomorphin affects a wide range of T cell function. In order to obtain the bigger picture of the effects of DM in T cell activation. transcriptomic analysis was performed using mouse primary CD25-CD4+ T cells with either DM (4 &#956;M) or vehicle in the presence or absence of stimulation by anti-CD3 and -CD28 antibodies.  Mouse CD4+ T cells were prepared and cultured with or without stimulation by plate bound anti-CD3 mAb and soluble anti-CD28 mAb for 1 hour. Subsequently, 4 &#956;M DM or DMSO was added and cells were incubated for 6 hours. Total RNA was isolated using Qiagen RNeasy mini kits.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27378</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27378/samples/</item></data></biogps>
