<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/GSE299nnn/GSE299673/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Mus musculus</species><gds_type>Methylation profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE299673</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Reduced Representation Bisulfite Sequencing of Mouse Hearts Following Cardiomyocyte-Specific DNMT3A Overexpression</name><description>Aging is associated with extensive epigenetic remodeling in cardiomyocytes, including increased DNA methylation. To investigate the causal role of DNA hypermethylation in age-related cardiac dysfunction, we overexpressed DNA methyltransferase 3A (DNMT3A) specifically in cardiomyocytes of young adult mice using a cardiac-specific AAV vector. Reduced representation bisulfite sequencing (RRBS) was performed on isolated cardiomyocyte nuclei from DNMT3A-overexpressing (Dnmt3a OE) and control (GFP) hearts. This dataset provides genome-wide DNA methylation profiles for both groups, enabling analysis of DNMT3A-driven methylome remodeling in the heart.</description><dates><publication>2026/06/12</publication></dates><accession>GSE299673</accession><cross_references><GSM>GSM9043484</GSM><GSM>GSM9043483</GSM><GSM>GSM9043486</GSM><GSM>GSM9043485</GSM><GSM>GSM9043488</GSM><GSM>GSM9043487</GSM><GSM>GSM9043489</GSM><GSM>GSM9043491</GSM><GSM>GSM9043490</GSM><GSM>GSM9043492</GSM><GPL>34290</GPL><GSE>299673</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>