{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326694/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Mus musculus"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE326694"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Transcriptomic profiling of primary mouse aortic smooth muscle cells treated with inflammatory macrophage-conditioned medium","description":"Inflammatory cell infiltration is a hallmark of many vascular diseases, but the specific molecular mechanisms by which macrophage-derived signals influence smooth muscle cell (SMC) phenotype remain poorly defined. This study utilized bulk RNA sequencing to elucidate the transcriptomic shifts driven by the inflammatory macrophage secretome.","dates":{"publication":"2026/06/03"},"accession":"GSE326694","cross_references":{"GSM":["GSM9637271","GSM9637272","GSM9637270","GSM9637275","GSM9637276","GSM9637273","GSM9637274","GSM9637268","GSM9637269","GSM9637277","GSM9637278","GSM9637267"],"GPL":["34290"],"GSE":["326694"],"taxon":["Mus musculus"],"PMID":["[41896892]"]}}