<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/GSE347nnn/GSE347403/</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=GSE347403</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Hippocampal interferon-response, unfolded-protein-response and synaptic transcriptional signatures in RORgt-transgenic mice</name><description>RORgt-transgenic mice provide a model of sustained Th17 bias. We performed bulk RNA sequencing of bilateral hippocampi from untreated 10-week-old male RORgt-transgenic mice and wild-type littermates (n = 3 per genotype) to characterize gene-level and gene-set transcriptional differences. RNA-seq identified a small set of FDR-significant genes and gene-set enrichment patterns involving interferon responses, unfolded protein response, and synaptic/calcineurin-related processes. The dataset is intended to support transparent reanalysis of the hippocampal transcriptomic phenotype associated with the RORgt-transgenic genotype.</description><dates><publication>2026/09/16</publication></dates><accession>GSE347403</accession><cross_references><GSM>GSM10052263</GSM><GSM>GSM10052264</GSM><GSM>GSM10052262</GSM><GSM>GSM10052267</GSM><GSM>GSM10052265</GSM><GSM>GSM10052266</GSM><GPL>37305</GPL><GSE>347403</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>