<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/GSE339nnn/GSE339246/</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=GSE339246</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq profiling of U-2 OS osteosarcoma cells expressing scrambled control or Timeless shRNA</name><description>Timeless and its fission yeast ortholog Swi1 are evolutionarily conserved components of the replication fork protection complex that ensures faithful DNA replication and genome stability. To elucidate the transcriptome-wide impact of Timeless depletion, we treated U-2 OS cells with lentiviruses expressing scrambled control or Timeless-targeting shRNA.</description><dates><publication>2026/08/19</publication></dates><accession>GSE339246</accession><cross_references><GSM>GSM9891801</GSM><GSM>GSM9891800</GSM><GSM>GSM9891802</GSM><GSM>GSM9891797</GSM><GSM>GSM9891799</GSM><GSM>GSM9891798</GSM><GPL>34284</GPL><GSE>339246</GSE><taxon>Homo sapiens</taxon><PMID>[42650843]</PMID></cross_references></HashMap>