<HashMap><database>GEO</database><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=GSE297196</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>m6A RIP-seq of beta-cell s from liver-specific insulin receptor knockout (LIRKO) mice</name><description>In type 2 diabetes, pancreatic beta-cells fail to compensate for the presence of insulin resistance in target tissues. Identifying and studying innovative molecular mechanisms that control the beta-cell adaptation to insulin resistance represent an interesting line of research and are necessary. N6-Methyladenosine (m6A) is the most abundant modification in mRNA and is found virtually in all mammals. Through m6A-profiling of Control and LIRKO islets we aimed to identify the m6A landscape of the successful beta-cell adaption to insulin resistance.</description><dates><publication>2026/05/14</publication></dates><accession>GSE297196</accession><cross_references><GSM>GSM8985458</GSM><GSM>GSM8985436</GSM><GSM>GSM8985437</GSM><GSM>GSM8985459</GSM><GSM>GSM8985438</GSM><GSM>GSM8985450</GSM><GSM>GSM8985451</GSM><GSM>GSM8985452</GSM><GSM>GSM8985430</GSM><GSM>GSM8985431</GSM><GSM>GSM8985453</GSM><GSM>GSM8985454</GSM><GSM>GSM8985432</GSM><GSM>GSM8985455</GSM><GSM>GSM8985433</GSM><GSM>GSM8985434</GSM><GSM>GSM8985456</GSM><GSM>GSM8985457</GSM><GSM>GSM8985435</GSM><GSM>GSM8985447</GSM><GSM>GSM8985448</GSM><GSM>GSM8985449</GSM><GSM>GSM8985427</GSM><GSM>GSM8985428</GSM><GSM>GSM8985429</GSM><GSM>GSM8985461</GSM><GSM>GSM8985462</GSM><GSM>GSM8985460</GSM><GPL>21103</GPL><GSE>297196</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>