<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Txt>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326856/suppl/filelist.txt</Txt><Raw>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326856/suppl/GSE326856_RAW.tar</Raw><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326856/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Rattus norvegicus</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=GSE326856</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell RNA-seq profiles of intestinal mucosa in IBS-D rats to explore the mechanism of immune barrier regulation in pathogenesis</name><description>We have employed a single cell sequencing approach using 10x Genomics scRNAseq to study isolated endothelial cells, immune cells and stromal cells from the intestinal mucosa of the control group and diarrhea-predominant irritable bowel syndrome (IBS-D) rats. This study systematically deciphered the transcriptional landscape of the colonic mucosa in a rat model of IBS-D at single-cell resolution, revealing compositional shifts, transcriptional signatures, and potential regulatory networks among various cellular subpopulations, including epithelial, immune, and stromal cells.</description><dates><publication>2026/07/08</publication></dates><accession>GSE326856</accession><cross_references><GSM>GSM9641327</GSM><GSM>GSM9641326</GSM><GSM>GSM9641325</GSM><GSM>GSM9641324</GSM><GPL>25947</GPL><GSE>326856</GSE><taxon>Rattus norvegicus</taxon></cross_references></HashMap>