<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/GSE325nnn/GSE325258/</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=GSE325258</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Residual p53 in HPV positive cervical cancer cells has gain of function properties</name><description>Human papillomavirus (HPV)-positive cervical cancer cells retain residual p53 despite E6-mediated degradation. To investigate whether this residual p53 has gain-of-function properties, CRISPR/Cas9 was used to generate p53 knockout HeLa clones and compare them with a WT control clone. RNA-seq profiling identified transcriptomic changes associated with loss of residual p53.</description><dates><publication>2026/05/13</publication></dates><accession>GSE325258</accession><cross_references><GSM>GSM9598554</GSM><GSM>GSM9598555</GSM><GSM>GSM9598552</GSM><GSM>GSM9598553</GSM><GSM>GSM9598550</GSM><GSM>GSM9598551</GSM><GPL>24676</GPL><GSE>325258</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>