<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/GSE181nnn/GSE181327/</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><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=GSE181327</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Epigenomic and transcriptomic features induced by silencing of ZNF280C in colon cancer cells and knock-out of Zfp280c in mice [RNA-Seq]</name><description>Znic finger proteins play crucial roles in development and disease, including tumorigenesis. Here, we identifed ZNF280C as a novel oncogenic driver in colorectal cancer, and systematically studied the molecular mechanisms underlying ZNF280C-mediated malignant transformation and progression.</description><dates><publication>2022/05/20</publication></dates><accession>GSE181327</accession><cross_references><GSM>GSM5494786</GSM><GSM>GSM5494787</GSM><GSM>GSM5494784</GSM><GSM>GSM5494785</GSM><GSM>GSM5494788</GSM><GSM>GSM5494789</GSM><GSM>GSM5494790</GSM><GSM>GSM5494793</GSM><GSM>GSM5494783</GSM><GSM>GSM5494794</GSM><GSM>GSM5494791</GSM><GSM>GSM5494792</GSM><GPL>23479</GPL><GPL>23227</GPL><SRA>SRP330880</SRA><GSE>181327</GSE><taxon> Mus musculus</taxon><taxon>Homo sapiens</taxon><PMID>[35605119]</PMID></cross_references></HashMap>