<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/GSE297nnn/GSE297670/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE297670</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Splice-altering TP53 missense mutations: Drivers of functional loss and therapeutic targets via RNA modulation</name><description>Using bacterial artificial chromosome DNA-mediated targeting, we developed knock-in TP53 mutant cell models including c.182A>G, c.318C>G, c.356C>G and c.362C>A. These missense mutations can function as frameshift or hypomorphic mutations due to aberrant splicing, significantly compromising TP53 mRNA integrity.</description><dates><publication>2026/05/31</publication></dates><accession>GSE297670</accession><cross_references><GSM>GSM8996382</GSM><GSM>GSM8996393</GSM><GSM>GSM8996394</GSM><GSM>GSM8996383</GSM><GSM>GSM8996391</GSM><GSM>GSM8996380</GSM><GSM>GSM8996381</GSM><GSM>GSM8996392</GSM><GSM>GSM8996390</GSM><GSM>GSM8996379</GSM><GSM>GSM8996388</GSM><GSM>GSM8996377</GSM><GSM>GSM8996378</GSM><GSM>GSM8996389</GSM><GSM>GSM8996386</GSM><GSM>GSM8996387</GSM><GSM>GSM8996384</GSM><GSM>GSM8996385</GSM><GPL>28038</GPL><GSE>297670</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>