<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/GSE338nnn/GSE338875/</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=GSE338875</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The Histone Demethylase KDM6B Restrains Hypermetabolic LYVE1+ Perivascular Macrophages and Preserves Adipogenic Balance [RNA-seq wat]</name><description>We employed a bulk RNA sequencing approach to study transcriptional remodeling of white adipose tissue in wild-type and macrophage-specific KDM6B knockout mice fed a high-fat diet for 5 weeks. Subcutaneous white adipose tissue and epididymal white adipose tissue were collected and analyzed, with three biological replicates per group. This study was designed to identify depot-specific and genotype-dependent gene expression changes associated with diet-induced obesity. These data provide insights into macrophage-dependent regulation of adipose tissue inflammation, metabolic dysfunction, extracellular matrix remodeling, and tissue adaptation during chronic high-fat diet feeding.</description><dates><publication>2026/09/01</publication></dates><accession>GSE338875</accession><cross_references><GSM>GSM9883960</GSM><GSM>GSM9883961</GSM><GSM>GSM9883962</GSM><GSM>GSM9883963</GSM><GSM>GSM9883964</GSM><GSM>GSM9883965</GSM><GSM>GSM9883954</GSM><GSM>GSM9883955</GSM><GSM>GSM9883956</GSM><GSM>GSM9883957</GSM><GSM>GSM9883958</GSM><GSM>GSM9883959</GSM><GPL>24247</GPL><GSE>338875</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>