<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/GSE337nnn/GSE337112/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE337112</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>MeRIP-seq profiling of m⁶A modifications in Alkbh5-KO and control bone marrow-derived macrophages following M1 polarization</name><description>We performed MeRIP-seq combined with RNA-seq to identify downstream targets of the m⁶A demethylase ALKBH5 in macrophages. Bone marrow-derived macrophages from myeloid-specific Alkbh5 knockout and Alkbh5-fl/fl littermate control mice were polarized to the M1 phenotype with LPS and IFN-γ. m⁶A-enriched RNA was immunoprecipitated using an anti-m⁶A antibody and sequenced on an Illumina NovaSeq 6000 platform. Altered m⁶A peaks in Alkbh5-KO cells were predominantly located within coding sequences, 3′ untranslated regions, and regions near stop codons. Integrative analysis with RNA-seq identified genes with both altered m⁶A methylation and differential expression, revealing the m⁶A epitranscriptomic landscape regulated by ALKBH5 in M1-polarized macrophages.</description><dates><publication>2026/09/03</publication></dates><accession>GSE337112</accession><cross_references><GSM>GSM9848347</GSM><GSM>GSM9848336</GSM><GSM>GSM9848337</GSM><GSM>GSM9848345</GSM><GSM>GSM9848346</GSM><GSM>GSM9848338</GSM><GSM>GSM9848339</GSM><GSM>GSM9848340</GSM><GSM>GSM9848343</GSM><GSM>GSM9848344</GSM><GSM>GSM9848341</GSM><GSM>GSM9848342</GSM><GPL>24247</GPL><GSE>337112</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>