<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/GSE338775/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE338775</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 [scRNA-Seq]</name><description>We employed single-cell RNA sequencing to study adipose tissue macrophages isolated from epididymal white adipose tissue of wild-type and macrophage-specific KDM6B knockout mice fed a high-fat diet for 5 weeks. This study was designed to identify macrophage subpopulations and genotype-dependent transcriptional changes associated with KDM6B deficiency during early diet-induced obesity. These data provide insights into macrophage heterogeneity, inflammatory activation, lipid-associated macrophage states, and immune remodeling in obese adipose tissue.</description><dates><publication>2026/09/01</publication></dates><accession>GSE338775</accession><cross_references><GSM>GSM9881329</GSM><GSM>GSM9881328</GSM><GSM>GSM9881339</GSM><GSM>GSM9881341</GSM><GSM>GSM9881330</GSM><GSM>GSM9881340</GSM><GSM>GSM9881338</GSM><GSM>GSM9881337</GSM><GSM>GSM9881336</GSM><GSM>GSM9881335</GSM><GSM>GSM9881334</GSM><GSM>GSM9881333</GSM><GSM>GSM9881343</GSM><GSM>GSM9881332</GSM><GSM>GSM9881331</GSM><GSM>GSM9881342</GSM><GPL>21103</GPL><GSE>338775</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>