<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/GSE348nnn/GSE348189/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE348189</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq analysis of TGF-beta1-stimulated human RPTEC/TERT1 cells treated with mesenchymal stem cell-conditioned media</name><description>Renal proximal tubular epithelial cell responses to mesenchymal stem cell-conditioned medium were examined in a TGF-beta1-induced profibrotic model. Human RPTEC/TERT1 cells were assigned to four conditions: untreated cells without TGF-beta1 or conditioned medium (NC); cells exposed to 10 ng/mL recombinant human TGF-beta1 for 24 h, followed by complete medium replacement with conditioned medium from immortalized human adipose-derived mesenchymal stem cells transfected with a negative-control miRNA mimic (TN) or a miR-29a-3p mimic (T29). TGF-beta1 was maintained at 10 ng/mL throughout the subsequent 48 h conditioned-medium treatment. Bulk mRNA sequencing was used to characterize condition-associated transcriptomic changes.</description><dates><publication>2026/09/23</publication></dates><accession>GSE348189</accession><cross_references><GSM>GSM10067663</GSM><GSM>GSM10067664</GSM><GSM>GSM10067662</GSM><GSM>GSM10067667</GSM><GSM>GSM10067668</GSM><GSM>GSM10067665</GSM><GSM>GSM10067666</GSM><GSM>GSM10067669</GSM><GSM>GSM10067670</GSM><GPL>30173</GPL><GSE>348189</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>