<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/GSE326nnn/GSE326591/</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=GSE326591</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of pancreatic islets in mice with ALIX deletion in PDGFRα⁺ mesenchymal progenitors under high-fat diet feeding</name><description>Using mice in which ALIX, a key regulator of small extracellular vesicle (sEV) biogenesis, was selectively deleted in PDGFRα⁺ mesenchymal progenitors (Pα-ALIXKO mice), we performed RNA sequencing of pancreatic islets isolated from control and Pα-ALIXKO mice under high-fat diet feeding. This dataset enables the analysis of transcriptomic changes in pancreatic islets derived from control and Pα-ALIXKO mice.</description><dates><publication>2026/08/31</publication></dates><accession>GSE326591</accession><cross_references><GSM>GSM9635160</GSM><GSM>GSM9635162</GSM><GSM>GSM9635161</GSM><GSM>GSM9635164</GSM><GSM>GSM9635163</GSM><GSM>GSM9635166</GSM><GSM>GSM9635165</GSM><GSM>GSM9635168</GSM><GSM>GSM9635167</GSM><GPL>24247</GPL><GSE>326591</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>