<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/GSE331nnn/GSE331360/</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=GSE331360</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Bulk RNA sequencing of bone marrow-derived macrophages from WT and Ch25h-KO mice under different treatment conditions</name><description>Bulk RNA-seq of bone marrow-derived macrophages (BMDMs) differentiated from WT and Ch25h-KO mice. BMDMs were treated with PBS (control), C. neoformans K99 strain, recombinant IL-4, or K99 combined with IL-4 for 18 hours. Gene expression was quantified to investigate the role of Ch25h in macrophage responses to fungal infection and type 2 cytokine signaling.</description><dates><publication>2026/05/19</publication></dates><accession>GSE331360</accession><cross_references><GSM>GSM9744626</GSM><GSM>GSM9744615</GSM><GSM>GSM9744614</GSM><GSM>GSM9744625</GSM><GSM>GSM9744624</GSM><GSM>GSM9744613</GSM><GSM>GSM9744635</GSM><GSM>GSM9744634</GSM><GSM>GSM9744623</GSM><GSM>GSM9744612</GSM><GSM>GSM9744619</GSM><GSM>GSM9744629</GSM><GSM>GSM9744618</GSM><GSM>GSM9744617</GSM><GSM>GSM9744628</GSM><GSM>GSM9744627</GSM><GSM>GSM9744616</GSM><GSM>GSM9744633</GSM><GSM>GSM9744622</GSM><GSM>GSM9744621</GSM><GSM>GSM9744632</GSM><GSM>GSM9744631</GSM><GSM>GSM9744620</GSM><GSM>GSM9744630</GSM><GPL>34328</GPL><GSE>331360</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>