<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/GSE301nnn/GSE301840/</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=GSE301840</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Life-saving left ventricular assist devices promote a transcriptomic signature favoring cardiac fatty acid metabolism, repair and anti-inflammation</name><description>In this study, we performed single-nuclei RNA sequencing on heart samples from 6 end-stage heart failure patients (3 ischemic cardiomyopathy and 3 non-ischemic cardiomyopathy). Each of these patients was treated with a left ventricular assist device (LVAD). Analysis of the longitudinal effect of LVAD at the transcriptomic level revealed a common signature profile related to the glucocorticoid receptor, independent of etiologies. Specifically, four genes promoting cardiac fatty acid metabolism, repair, and anti-inflammatory action were highlighted: FKBP5, ZBTB16, FOXO3, and PDK4.</description><dates><publication>2026/05/15</publication></dates><accession>GSE301840</accession><cross_references><GSM>GSM9090706</GSM><GSM>GSM9090707</GSM><GSM>GSM9090704</GSM><GSM>GSM9090705</GSM><GSM>GSM9090702</GSM><GSM>GSM9090703</GSM><GSM>GSM9090700</GSM><GSM>GSM9090701</GSM><GSM>GSM9090698</GSM><GSM>GSM9090699</GSM><GSM>GSM9090708</GSM><GSM>GSM9090709</GSM><GPL>24676</GPL><GSE>301840</GSE><taxon>Homo sapiens</taxon><PMID>[42019320]</PMID></cross_references></HashMap>