<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/GSE310nnn/GSE310464/</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=GSE310464</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Microprotein miP-FERMT3 modulates endothelial cell protein catabolism and induces p53-mediated cell cycle arrest and senescence</name><description>In this study, the function of a novel 69 amino acid microprotein (miP) encoded by a smORF within the coding sequence of the FERM Domain Containing Kindlin-3 transcript, i.e. miP-FERMT3, was investigated.</description><dates><publication>2026/07/01</publication></dates><accession>GSE310464</accession><cross_references><GSM>GSM9301749</GSM><GSM>GSM9301747</GSM><GSM>GSM9301758</GSM><GSM>GSM9301759</GSM><GSM>GSM9301748</GSM><GSM>GSM9301756</GSM><GSM>GSM9301757</GSM><GSM>GSM9301765</GSM><GSM>GSM9301754</GSM><GSM>GSM9301755</GSM><GSM>GSM9301766</GSM><GSM>GSM9301752</GSM><GSM>GSM9301763</GSM><GSM>GSM9301753</GSM><GSM>GSM9301764</GSM><GSM>GSM9301750</GSM><GSM>GSM9301761</GSM><GSM>GSM9301762</GSM><GSM>GSM9301751</GSM><GSM>GSM9301760</GSM><GPL>30173</GPL><GSE>310464</GSE><taxon>Homo sapiens</taxon><PMID>[42343301]</PMID></cross_references></HashMap>