<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/GSE298nnn/GSE298180/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE298180</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>METTL3-dependent m6A methylation in atherogenic endothelial inflammation [RNA]</name><description>Atherosclerosis is initiated by endothelial inflammation. Using RNA-seq and eCLIP, we identified METTL3 as a mechanosensitive m6A writer that upregulates NLRP1 and downregulates KLF4 through YTHDF readers. Knockdown of METTL3 abrogated these changes and protected against flow-induced atherogenesis in vitro and in vivo.</description><dates><publication>2026/06/26</publication></dates><accession>GSE298180</accession><cross_references><GSM>GSM9009587</GSM><GSM>GSM9009586</GSM><GSM>GSM9009585</GSM><GSM>GSM9009584</GSM><GSM>GSM9009589</GSM><GSM>GSM9009588</GSM><GSM>GSM9009583</GSM><GSM>GSM9009582</GSM><GSM>GSM9009581</GSM><GPL>16791</GPL><GSE>298180</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>