<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/GSE335nnn/GSE335106/</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=GSE335106</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Bulk RNAseq analysis of wildtype and Pim1-/- macrophages</name><description>PIM1 is a serine/threonine kinase that modulates immune responses and cellular metabolism. To examine the function of PIM1 in macrophage gene expression, peritoneal macrophages were isolated from wild-type and Pim1-/- mice. They were treated with 20 μg/mL oxidized low-density lipoprotein for 8 hours. Total RNA was extracted and analyzed using bulk RNA sequencing to compare gene expression profiles and identify differentially regulated pathways between wild-type and Pim1-/- macrophages.</description><dates><publication>2026/06/15</publication></dates><accession>GSE335106</accession><cross_references><GSM>GSM9805890</GSM><GSM>GSM9805880</GSM><GSM>GSM9805881</GSM><GSM>GSM9805882</GSM><GSM>GSM9805883</GSM><GSM>GSM9805884</GSM><GSM>GSM9805885</GSM><GSM>GSM9805886</GSM><GSM>GSM9805887</GSM><GSM>GSM9805888</GSM><GSM>GSM9805889</GSM><GSM>GSM9805879</GSM><GPL>17021</GPL><GSE>335106</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>