<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/GSE314nnn/GSE314809/</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=GSE314809</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq analysis of pericytes with OPA1 overexpression</name><description>Chronic allograft dysfunction (CAD) is the leading cause of long-term kidney transplant failure, characterized by pericyte-to-myofibroblast transition (PMT)-driven progressive interstitial fibrosis. We identified that OPA1-containing extracellular vesicles from autophagy-deficient endothelial cells promote PMT through dual ROS-dependent pathways. This dataset contains RNA-seq data from C3H10T1/2 pericytes with or without OPA1 overexpression to investigate the transcriptional changes during PMT.</description><dates><publication>2026/08/30</publication></dates><accession>GSE314809</accession><cross_references><GSM>GSM9411032</GSM><GSM>GSM9411034</GSM><GSM>GSM9411033</GSM><GSM>GSM9411036</GSM><GSM>GSM9411035</GSM><GSM>GSM9411037</GSM><GPL>24247</GPL><GSE>314809</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>