<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/GSE297nnn/GSE297074/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE297074</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>m6A Regulator ALKBH5 Binbing RNA Identified by eCLIP in Human beta-cell line EndoC-bH1</name><description>N6-methyladenosine (m6A) is the most abundant chemical modification in mRNA. However, the role of m6A and the precise mechanisms involved in the beta-cell adaptation to metabolic demand are unexplored. Here, we performed enhanced crosslinking and immunoprecipitation (eCLIP) assays to identify m6A sites regulated by ALKBH5 in EndoC-bh1 human beta-cells.</description><dates><publication>2026/05/13</publication></dates><accession>GSE297074</accession><cross_references><GSM>GSM8983400</GSM><GSM>GSM8983399</GSM><GSM>GSM8983398</GSM><GSM>GSM8983397</GSM><GSM>GSM8983404</GSM><GSM>GSM8983403</GSM><GSM>GSM8983402</GSM><GSM>GSM8983401</GSM><GPL>16791</GPL><GSE>297074</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>