<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/GSE345nnn/GSE345972/</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=GSE345972</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic analysis of the effects of Poly I:C on islet cells in NOD mice</name><description>The relationship of autoimmune type 1 diabetes (T1D) and natural killer (NK) cells remains unclear. Poly inosine:cytidine (PolyI:C) is a double-stranded RNA mimic that activates an anti-viral response through TLR3 signaling and leads to activation of NK cells. Here we administered PolyI:C to female NOD mice in order to understand how NK cell activation changes the islet microenvironment by altering transcriptomes of islet cells.</description><dates><publication>2026/09/14</publication></dates><accession>GSE345972</accession><cross_references><GSM>GSM10020079</GSM><GSM>GSM10020078</GSM><GSM>GSM10020077</GSM><GSM>GSM10020076</GSM><GSM>GSM10020075</GSM><GSM>GSM10020074</GSM><GSM>GSM10020084</GSM><GSM>GSM10020083</GSM><GSM>GSM10020082</GSM><GSM>GSM10020081</GSM><GSM>GSM10020080</GSM><GPL>21103</GPL><GSE>345972</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>