{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Xu M"],"funding":["Priority Academic Program Development of Jiangsu Higher Education Institutions","National Natural Science Foundation of China","Second Affiliated Hospital of Soochow University"],"pagination":["855645"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8980722"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13"],"pubmed_abstract":["<h4>Background</h4>Ulcerative colitis (UC) is an inflammatory disease of the intestinal mucosa, and its incidence is steadily increasing worldwide. Intestinal immune dysfunction has been identified as a central event in UC pathogenesis. However, the underlying mechanisms that regulate dysfunctional immune cells and inflammatory phenotype remain to be fully elucidated.<h4>Methods</h4>Transcriptome profiling of intestinal mucosa biopsies were downloaded from the GEO database. Robust Rank Aggregation (RRA) analysis was performed to identify statistically changed genes and differentially expressed genes (DEGs). Gene Set Enrichment Analysis (GSEA), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to explore potential biological mechanisms. CIBERSORT was used to e"],"journal":["Frontiers in immunology"],"pubmed_title":["Identification of Immune-Related Gene Signature and Prediction of CeRNA Network in Active Ulcerative Colitis."],"pmcid":["PMC8980722"],"funding_grant_id":["81820108023, 2018YFC1705505"],"pubmed_authors":["Lv J","Chen N","Chin YE","Xu M","Peng W","Zhu J","Zi R","Zeng Y","Jiang M","Wang Y","Kong Y","Yue J"],"additional_accession":[]},"is_claimable":false,"name":"Identification of Immune-Related Gene Signature and Prediction of CeRNA Network in Active Ulcerative Colitis.","description":"<h4>Background</h4>Ulcerative colitis (UC) is an inflammatory disease of the intestinal mucosa, and its incidence is steadily increasing worldwide. Intestinal immune dysfunction has been identified as a central event in UC pathogenesis. However, the underlying mechanisms that regulate dysfunctional immune cells and inflammatory phenotype remain to be fully elucidated.<h4>Methods</h4>Transcriptome profiling of intestinal mucosa biopsies were downloaded from the GEO database. Robust Rank Aggregation (RRA) analysis was performed to identify statistically changed genes and differentially expressed genes (DEGs). Gene Set Enrichment Analysis (GSEA), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to explore potential biological mechanisms. CIBERSORT was used to e","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2026-04-08T17:24:14.548Z","creation":"2025-04-04T23:04:27.042Z"},"accession":"S-EPMC8980722","cross_references":{"pubmed":["35392084"],"doi":["10.3389/fimmu.2022.855645"]}}