<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/GSE280nnn/GSE280871/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Danio rerio</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=GSE280871</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Identifying transcription factors distinguishing regenerating cardiomyocytes in the zebrafish heart using single cell transcriptomics</name><description>Zebrafish hearts present a remarkable regenerative capacity upon injury, constituting a valuable source of information for cardiomyocyte (CM) cycle re-entry/proliferation. Understanding which factors contribute for zebrafish heart regeneration is crucial for developing regeneration-inducing strategies as mammalian hearts are limited in regenerative capacity. Exploring further our recently published optimized approach for increasing the single cell RNA sequencing (scRNA-seq) resolution specifically CMs, we have systematically evaluated transcription factors (TFs) defining regenerating zebrafish CMs. Here, after the scRNA-seq analysis, we observed a CM cycling cluster exclusively present in zebrafish injured hearts, which allowed us to identify potential TFs.</description><dates><publication>2026/09/01</publication></dates><accession>GSE280871</accession><cross_references><GSM>GSM8606770</GSM><GSM>GSM8606769</GSM><GSM>GSM8606768</GSM><GPL>24995</GPL><GSE>280871</GSE><taxon>Danio rerio</taxon></cross_references></HashMap>