<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/GSE304nnn/GSE304678/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Rattus norvegicus</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=GSE304678</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Cytokine-signaling single cell Seq</name><description>The design of this experiment was to identify early response genes after exposure to a cytokine associated with tissue resident macrophages. The highly glucose responsive insulinoma cell line (832/13) was subcloned from INS-1 cells, a cell line derived from rat beta-cells. 832/13 cells were used as the experimental model. The design wase exposure of 832/13 cells to either no treatment or 1ng/mL IL-1b for 3 h. At the end of the 3h period, the 832/13 cells were removed from monolayer culture and placed into a single cell suspension for library construction.</description><dates><publication>2026/09/23</publication></dates><accession>GSE304678</accession><cross_references><GSM>GSM9155156</GSM><GSM>GSM9155158</GSM><GSM>GSM9155157</GSM><GPL>20084</GPL><GSE>304678</GSE><taxon>Rattus norvegicus</taxon><PMID>[42572286]</PMID></cross_references></HashMap>