<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE318nnn/GSE318699/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318699</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNAseq of mAECs cultured in normal medium or treated with the supernatant from TNFα+CD68+ macrophages</name><description>We isolated TNFα+CD68+ macrophages from atherosclerotic mice, and transferred the conditioned medium to normal murine aortic endothelial cells (mAECs). mAECs cultured in normal medium was used as the negative control. Following a 48-h incubation in conditioned media, mAECs were subjected to bulk RNA-sequencing analysis.</description><dates><publication>2026/05/09</publication></dates><accession>GSE318699</accession><cross_references><GSM>GSM9500939</GSM><GSM>GSM9500938</GSM><GSM>GSM9500941</GSM><GSM>GSM9500940</GSM><GPL>19057</GPL><GSE>318699</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>