<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/GSE318nnn/GSE318188/</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>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318188</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>GDF15 impacts chronic kidney disease and associated cachexia through distinct mechanisms</name><description>Chronic kidney disease (CKD) is frequently accompanied by cachexia and substantial metabolic alterations, including anorexia, muscle/fat wasting, and inflammation, which collectively contribute topoor clinical outcomes.However, the underlying molecular mechanisms remain poorly understood. This study demonstrates that growth differentiation factor 15 (GDF15) plays a pivotal role in CKD-associated cachexia and molecular changes.</description><dates><publication>2026/09/10</publication></dates><accession>GSE318188</accession><cross_references><GSM>GSM9488803</GSM><GSM>GSM9488802</GSM><GSM>GSM9488801</GSM><GSM>GSM9488800</GSM><GSM>GSM10042233</GSM><GSM>GSM10042234</GSM><GSM>GSM10042235</GSM><GSM>GSM10042236</GSM><GSM>GSM10042237</GSM><GSM>GSM10042238</GSM><GSM>GSM10042239</GSM><GSM>GSM9488795</GSM><GSM>GSM9488811</GSM><GSM>GSM9488810</GSM><GSM>GSM9488799</GSM><GSM>GSM9488798</GSM><GSM>GSM9488797</GSM><GSM>GSM9488796</GSM><GSM>GSM10042244</GSM><GSM>GSM9488809</GSM><GSM>GSM9488808</GSM><GSM>GSM9488807</GSM><GSM>GSM10042240</GSM><GSM>GSM10042241</GSM><GSM>GSM9488806</GSM><GSM>GSM10042242</GSM><GSM>GSM9488805</GSM><GSM>GSM9488804</GSM><GSM>GSM10042243</GSM><GPL>34290</GPL><GSE>318188</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>