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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="GSM1409243"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409243"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409243"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409243"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409247"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409247"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409247"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409247"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409247"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">FACS sorted brain-derived SMC/pericyte cells</item></item></item><item><item key="GSM1409252"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">aorta explants</item></item></item><item><item key="GSM1409252"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">aorta explants</item></item></item><item><item key="GSM1409252"><item key="GENOTYPE">NOTCH3 +/-</item><item key="ORGANISM PART">aorta explants</item></item></item><item><item key="GSM1409255"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">aorta explants</item></item></item><item><item key="GSM1409255"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">aorta explants</item></item></item><item><item key="GSM1409255"><item key="GENOTYPE">NOTCH3 -/-</item><item key="ORGANISM PART">aorta explants</item></item></item></item><item key="id">7660</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Using a hitherto uncharacterized knockout mouse model of Notch 3, a Notch signaling receptor paralogue highly expressed in vascular SMCs,...</item><item key="geo_gse_id">E-GEOD-58368</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">15</item><item key="tags"><item>brain</item><item>notch</item><item>stroke</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">linking-notch-signaling-to-ischemic-stroke</item><item key="geo_id_plat">E-GEOD-58368_A-AFFY-45</item><item key="name">Linking Notch signaling to ischemic stroke</item><item key="created">Nov.12, 2014</item><item key="summary">Using a hitherto uncharacterized knockout mouse model of Notch 3, a Notch signaling receptor paralogue highly expressed in vascular SMCs, we uncover a striking susceptibility to ischemic stroke upon challenge. Cellular and molecular analyses of vascular SMCs derived from these animals associate Notch 3 activity to the expression of specific gene targets, whereas genetic rescue experiments unambiguously link Notch 3 function in vessels to the ischemic phenotype. Microarray Studies. Biotinylated cRNA samples from freshly sorted brain SMCs (four Notch 3 +/&#8722; mice and five Notch 3 &#8722;/&#8722; mice) were fragmented before hybridization (15 &#956;g each) onto mouse 430 2.0 Affymetrix chips. The chips were washed, stained by using strepavidin-phycoerytrin, and scanned the next day as described in ref. 24. For data normalization, all probe sets were scaled to a target intensity of 150. Microarray data analysis was performed by using Rosetta Resolver. All cells were from 10- to 12-week-old male mice. Gene Ontology Analyses. PANTHER software was used to define over- and underrepresented functions in the list of signature genes found by microarray analysis (25). P values were calculated by using binomial statistics.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-58368</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-58368/samples/</item></data></biogps>
