<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/GSE295nnn/GSE295694/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Non-coding RNA profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE295694</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Small RNA sequencing of adipose tissue derived extracellular vesicles from chow- or HFD-fed male mice</name><description>We identified EVs as novel regulatory factors that mediate adipose tissue–brain communication and are crucial for the central control of whole-body energy homeostasis. Our findings reveal that AT-EVs and their cargo microRNAs (miRNAs) are crucial regulators of central leptin sensitivity. To identify the specific subtypes of miRNAs that responsible for central leptin-sensitizing, we examined the sRNA profiles of EVs extracted from adipose tissue of healthy chow-fed and high-fat diet mice by RNA deep sequencing.</description><dates><publication>2026/04/10</publication></dates><accession>GSE295694</accession><cross_references><GSM>GSM8955308</GSM><GSM>GSM8955307</GSM><GSM>GSM8955304</GSM><GSM>GSM8955303</GSM><GSM>GSM8955306</GSM><GSM>GSM8955305</GSM><GSM>GSM8955302</GSM><GPL>17021</GPL><GSE>295694</GSE><taxon>Mus musculus</taxon><PMID>[41223857]</PMID></cross_references></HashMap>