<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/GSE330nnn/GSE330909/</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=GSE330909</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>TGFβ-Dependent Epithelial–Mesenchymal Plasticity in Immortalized Human Atrial Epicardial Cells: An mRNA Profiling Study</name><description>The adult mammalian heart exhibits limited regenerative capacity, and a stable adult human in vitro model for investigating epicardial activation remain limited. Here, we isolated human epicardium-derived cells from the adult heart auricle. Successful immortalization led to the generation of a stable immortalized epicardium-derived cell (iEPDC) population, allowing the investigation of intercellular dynamics upon EMT activation. TGFβ signalling was modulated using SB431542 or TGFβ3.</description><dates><publication>2026/07/23</publication></dates><accession>GSE330909</accession><cross_references><GSM>GSM9735519</GSM><GSM>GSM9735528</GSM><GSM>GSM9735517</GSM><GSM>GSM9735529</GSM><GSM>GSM9735518</GSM><GSM>GSM9735526</GSM><GSM>GSM9735527</GSM><GSM>GSM9735516</GSM><GSM>GSM9735524</GSM><GSM>GSM9735525</GSM><GSM>GSM9735522</GSM><GSM>GSM9735523</GSM><GSM>GSM9735520</GSM><GSM>GSM9735521</GSM><GSM>GSM9735530</GSM><GPL>34284</GPL><GSE>330909</GSE><taxon>Homo sapiens</taxon><PMID>[42505420]</PMID></cross_references></HashMap>