<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/GSE332nnn/GSE332752/</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=GSE332752</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptome of mouse colon under radiation injury and syringin treatment</name><description>This study performed transcriptome RNA sequencing on 15 mouse colon samples, including 5 blank control samples, 5 abdominal ionizing radiation (IR)-induced intestinal injury samples, and 5 syringin-treated injury samples. The aim was to identify gene expression changes and key regulatory pathways involved in radiation-induced intestinal damage and the protective mechanism of syringin. Differentially expressed genes (DEGs) were analyzed to explore mechanisms related to ferroptosis, the hnRNPA3-ESRRG-AIFM2-FSP1 regulatory axis, and gut-brain axis communication. These data provide a valuable transcriptomic resource for understanding radiation-induced intestinal injury and the transcriptomic responses to syringin in mouse colon tissue.</description><dates><publication>2026/09/03</publication></dates><accession>GSE332752</accession><cross_references><GSM>GSM9752948</GSM><GSM>GSM9752937</GSM><GSM>GSM9752936</GSM><GSM>GSM9752947</GSM><GSM>GSM9752939</GSM><GSM>GSM9752938</GSM><GSM>GSM9752940</GSM><GSM>GSM9752942</GSM><GSM>GSM9752941</GSM><GSM>GSM9752944</GSM><GSM>GSM9752943</GSM><GSM>GSM9752935</GSM><GSM>GSM9752946</GSM><GSM>GSM9752945</GSM><GSM>GSM9752934</GSM><GPL>24247</GPL><GSE>332752</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>