<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang R</submitter><funding>National Natural Science Foundation of China</funding><pagination>2629</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9454849</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(17)</volume><pubmed_abstract>Atrial fibrillation (AF) is a form of sustained cardiac arrhythmia and microRNAs (miRs) play crucial roles in the pathophysiology of AF. To identify novel miR-mRNA pairs, we performed RNA-seq from atrial biopsies of persistent AF patients and non-AF patients with normal sinus rhythm (SR). Differentially expressed miRs (11 down and 9 up) and mRNAs (95 up and 82 down) were identified and hierarchically clustered in a heat map. Subsequently, GO, KEGG, and GSEA analyses were run to identify deregulated pathways. Then, miR targets were predicted in the miRDB database, and a regulatory network of negatively correlated miR-mRNA pairs was constructed using Cytoscape. To select potential candidate genes from GSEA analysis, the top-50 enriched genes in GSEA were overlaid with predicted targets of di</pubmed_abstract><journal>Cells</journal><pubmed_title>Integrated Analysis of the microRNA-mRNA Network Predicts Potential Regulators of Atrial Fibrillation in Humans.</pubmed_title><pmcid>PMC9454849</pmcid><funding_grant_id>81970282</funding_grant_id><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Han W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Bektik E</pubmed_authors><pubmed_authors>Meng X</pubmed_authors><pubmed_authors>Sakon P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integrated Analysis of the microRNA-mRNA Network Predicts Potential Regulators of Atrial Fibrillation in Humans.</name><description>Atrial fibrillation (AF) is a form of sustained cardiac arrhythmia and microRNAs (miRs) play crucial roles in the pathophysiology of AF. To identify novel miR-mRNA pairs, we performed RNA-seq from atrial biopsies of persistent AF patients and non-AF patients with normal sinus rhythm (SR). Differentially expressed miRs (11 down and 9 up) and mRNAs (95 up and 82 down) were identified and hierarchically clustered in a heat map. Subsequently, GO, KEGG, and GSEA analyses were run to identify deregulated pathways. Then, miR targets were predicted in the miRDB database, and a regulatory network of negatively correlated miR-mRNA pairs was constructed using Cytoscape. To select potential candidate genes from GSEA analysis, the top-50 enriched genes in GSEA were overlaid with predicted targets of di</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-04T03:24:32.611Z</modification><creation>2025-04-04T03:24:32.611Z</creation></dates><accession>S-EPMC9454849</accession><cross_references><pubmed>36078037</pubmed><doi>10.3390/cells11172629</doi></cross_references></HashMap>