<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/GSE290nnn/GSE290000/</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><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE290000</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>CD36/FABP5/PPARδ signaling axis defines spontaneously proliferating cardiomyocytes in neonatal stages</name><description>Spontaneously cycling cardiomyocytes (CMs) represent a rare and unique population in the neonatal heart with the potential to drive cardiac regeneration in adulthood. While previous studies have observed their existence, the mechanisms regulating their cell cycle activity remain poorly understood. Here, we aim to identify the signaling axis that defines the spontaneously proliferating CMs in the neonatal stage.</description><dates><publication>2026/02/19</publication></dates><accession>GSE290000</accession><cross_references><GSM>GSM8803335</GSM><GSM>GSM8803334</GSM><GSM>GSM8803337</GSM><GSM>GSM8803336</GSM><GSM>GSM8803338</GSM><GSM>GSM8803331</GSM><GSM>GSM8803330</GSM><GSM>GSM8803333</GSM><GSM>GSM8803332</GSM><GPL>24247</GPL><GSE>290000</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>