<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/GSE337nnn/GSE337821/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE337821</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Inhibition of fatty acid binding protein 4 alleviates psoriasis-like skin inflammation by modulating macrophage polarization</name><description>This study provides single-cell RNA-seq profiles of human psoriasis lesional skin samples generated using the 10x Genomics single-cell platform. Human skin biopsies were dissociated into single-cell suspensions and processed for 10x Genomics 5' single-cell RNA-seq. Processed data include filtered feature-barcode matrices containing raw UMI counts. For SNP-multiplexed libraries, barcode-level sample assignment was performed using Demuxalot, and Demuxalot assignment files are provided together with the processed count matrices. These data enable cell-type-level analysis of immune and stromal cell populations in human psoriasis skin.</description><dates><publication>2026/08/26</publication></dates><accession>GSE337821</accession><cross_references><GSM>GSM9861014</GSM><GSM>GSM9861013</GSM><GSM>GSM9861012</GSM><GSM>GSM9861011</GSM><GSM>GSM9861010</GSM><GPL>24676</GPL><GSE>337821</GSE><taxon>Homo sapiens</taxon><PMID>[42609463]</PMID></cross_references></HashMap>