<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><omics_type>Multiomics</omics_type><center_name>Medical Microbiology and Immunology, University of Toledo College of Medicine</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA139167</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>To investigate the functional properties of Ly6G+ DC, we employed GeneChip analysis to compare the gene expression profiles between Ly6G+ DC and Ly6C- DC. Overall design: Crude bone marrow (BM) cells prepared from C57BL/6 mice were cultured in the presence of GM-CSF. On day 6, CD11c+/MHC II+/Ly6G+ cells and CD11c+/MHC II+/Ly6G- cells were simultaneously sorted from the same cultures by FACSAria. Total RNA were extracted and hybridized on Affymetrix microarrays.</long_description><tag>xref:PubMed:23305731</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Mus musculus</name><description>Expression data from Ly6G+ and Ly6G- dendritic cells (DC)</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-02-11</first_public></dates><accession>PRJNA139167</accession><cross_references><GEO>GSE28408</GEO><taxon>10090</taxon><PubMed>23305731</PubMed></cross_references></HashMap>