<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/GSE308nnn/GSE308534/</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=GSE308534</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq of paraventricular thalamus (PVT) and posterior insular cortex (pIC) in a mouse model of STZ-induced painful diabetic neuropathy with anxiety-like behavior</name><description>We generated poly(A)-selected, stranded mRNA-seq profiles from the paraventricular thalamus (PVT) and posterior insular cortex (pIC) of mice with streptozotocin (STZ; 200 mg/kg, i.p.)–induced painful diabetic neuropathy (PDN) and anxiety-like behavior, alongside vehicle controls. Twenty brain tissue samples (PVT and pIC from PDN and control groups) were sequenced. The dataset enables region-wise differential expression analysis and comparison of convergent versus region-specific remodeling between PVT and pIC.</description><dates><publication>2026/05/30</publication></dates><accession>GSE308534</accession><cross_references><GSM>GSM9247661</GSM><GSM>GSM9247662</GSM><GSM>GSM9247663</GSM><GSM>GSM9247652</GSM><GSM>GSM9247653</GSM><GSM>GSM9247664</GSM><GSM>GSM9247670</GSM><GSM>GSM9247671</GSM><GSM>GSM9247660</GSM><GSM>GSM9247669</GSM><GSM>GSM9247658</GSM><GSM>GSM9247659</GSM><GSM>GSM9247654</GSM><GSM>GSM9247665</GSM><GSM>GSM9247666</GSM><GSM>GSM9247655</GSM><GSM>GSM9247656</GSM><GSM>GSM9247667</GSM><GSM>GSM9247657</GSM><GSM>GSM9247668</GSM><GPL>34290</GPL><GSE>308534</GSE><taxon>Mus musculus</taxon><PMID>[42203788]</PMID></cross_references></HashMap>