<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/GSE334nnn/GSE334689/</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> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE334689</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>m6Am-seq profiling of macrophage-specific Pcif1 knockout mice during experimental colitis</name><description>Inflammatory bowel disease (IBD) is characterized by chronic intestinal inflammation accompanied by alterations in immune cell function and enteric nervous system homeostasis. To investigate the role of PCIF1-mediated N6,2′-O-dimethyladenosine (m6Am) RNA methylation in macrophages during colitis, we generated macrophage-specific Pcif1 knockout mice and performed transcriptome-wide RNA sequencing (RNA-seq) and m6Am profiling (m6Am-seq). These datasets were generated to characterize m6Am-regulated gene expression programs and identify molecular pathways associated with extracellular matrix remodeling, macrophage function, and enteric neuronal regulation during intestinal inflammation.</description><dates><publication>2026/08/07</publication></dates><accession>GSE334689</accession><cross_references><GSM>GSM9793361</GSM><GSM>GSM9793360</GSM><GSM>GSM9793363</GSM><GSM>GSM9793362</GSM><GSM>GSM9793365</GSM><GSM>GSM9793364</GSM><GSM>GSM9793358</GSM><GSM>GSM9793359</GSM><GPL>21273</GPL><GSE>334689</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>