<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/GSE343nnn/GSE343588/</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=GSE343588</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of imatinib on cisplatin-induced nephrotoxicity in mice</name><description>Cisplatin is a chemotherapeutic agent that induces proximal tubule injury in the kidneys. We aimed at exploring the effect of imatinib, a Tyrosine Kinase Inhibitor (THI), on the entry of cisplatin in proximal tubular cells and on cisplatin-induced DNA damage. RNA sequencing was performed in whole kidneys of mice (control groupe, n=4, 20mg/kg cisplatin-treated mice, n=4, 20mg/kg cisplatin + 150mg/kg imatinib-treated mice, n=4), which were collected 3 days after cisplatin intraperitoneal injection. In the cisplatin + imatinib group, imatinib was injected the day before cisplatin injection, and every day until the mice were euthanized.</description><dates><publication>2026/08/17</publication></dates><accession>GSE343588</accession><cross_references><GSM>GSM9957843</GSM><GSM>GSM9957844</GSM><GSM>GSM9957845</GSM><GSM>GSM9957846</GSM><GSM>GSM9957840</GSM><GSM>GSM9957841</GSM><GSM>GSM9957842</GSM><GSM>GSM9957847</GSM><GSM>GSM9957848</GSM><GSM>GSM9957849</GSM><GSM>GSM9957838</GSM><GSM>GSM9957839</GSM><GPL>30172</GPL><GSE>343588</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>