<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/GSE305nnn/GSE305407/</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=GSE305407</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>GPR35+ tumor-associated neutrophils promote tumor growth in hepatocellular carcinoma.</name><description>Bulk RNA-seq profiling of tumor-associated neutrophils from Hepa1-6 mouse hepatocellular carcinoma (HCC) models. Neutrophils were isolated from mice HCC tissues and classified as GPR35+ or GPR35- subsets (n=3 per group). Differential expression analysis revealed significant upregulation of MAPK signaling pathway and pathways associated with neutrophil migration and cytokines production in GPR35+ neutrophils. These data support the pro-tumorigenic role of GPR35+ neutrophils in HCC.</description><dates><publication>2026/04/05</publication></dates><accession>GSE305407</accession><cross_references><GSM>GSM9176661</GSM><GSM>GSM9176660</GSM><GSM>GSM9176656</GSM><GSM>GSM9176658</GSM><GSM>GSM9176657</GSM><GSM>GSM9176659</GSM><GPL>24247</GPL><GSE>305407</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>