<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/GSE243nnn/GSE243847/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE243847</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Differently expressed genes between the GP and NC groups</name><description>To further investigate the molecular mechanism underlying these changes in metabolites in relation to tumor progression, we conducted RNA-seq analysis. This analysis identified a total of 180 differentially expressed genes (DEGs; 132 upregulated and 48 downregulated) between the GP and NC groups. Subsequently, pathway analysis assigned these DEGs to 68 pathways, of which 38 showed significant enrichment in KEGG pathways (P &lt; 0.05).</description><dates><publication>2026/09/10</publication></dates><accession>GSE243847</accession><cross_references><GSM>GSM7796653</GSM><GSM>GSM7796654</GSM><GSM>GSM7796662</GSM><GSM>GSM7796660</GSM><GSM>GSM7796661</GSM><GSM>GSM7796659</GSM><GSM>GSM7796657</GSM><GSM>GSM7796658</GSM><GSM>GSM7796655</GSM><GSM>GSM7796656</GSM><GPL>24676</GPL><GSE>243847</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>