<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/GSE318nnn/GSE318951/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE318951</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of neonatal mouse ventricular myocytes (NMVMs) under hypoxia and recombinant Serglycin stimulation</name><description>To investigate the direct regulatory effects of Serglycin (SRGN) on cardiomyocytes under ischemic conditions, we performed bulk RNA-sequencing on primary neonatal mouse ventricular myocytes (NMVMs). The study includes three experimental groups: Control (Con), Hypoxia, and Hypoxia + recombinant SRGN (rSRGN). NMVMs in the Hypoxia and Hypoxia+rSRGN groups were subjected to oxygen-glucose deprivation (glucose-free and serum-free DMEM) in an anaerobic environment (AnaeroPack-MIC, Mitsubishi A-07) for 6 hours. This dataset identifies the transcriptional alterations driven by SRGN in cardiomyocytes during hypoxic stress.</description><dates><publication>2026/06/25</publication></dates><accession>GSE318951</accession><cross_references><GSM>GSM9506805</GSM><GSM>GSM9506803</GSM><GSM>GSM9506804</GSM><GSM>GSM9506797</GSM><GSM>GSM9506798</GSM><GSM>GSM9506801</GSM><GSM>GSM9506802</GSM><GSM>GSM9506799</GSM><GSM>GSM9506800</GSM><GPL>24247</GPL><GSE>318951</GSE><taxon>Mus musculus</taxon><PMID>[42327787]</PMID></cross_references></HashMap>