<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bencun M</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Klaus Tschira Foundation</funding><pagination>391</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8962266</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>Cardiovascular disease is still the leading cause of morbidity and mortality worldwide. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have become a valuable widespread in vitro model to study cardiac disease. Herein, we employ the hiPSC-CM model to identify novel miRNA-mRNA interaction partners during cardiac differentiation and β-adrenergic stress. Whole transcriptome and small RNA sequencing data were combined to identify novel miRNA-mRNA interactions. Briefly, mRNA and miRNA expression profiles were integrated with miRNA target predictions to identify significant statistical dependencies between a miRNA and its candidate target set. We show by experimental validation that our approach discriminates true from false miRNA target predictions. Thereby, we identified</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>New Tricks with Old Dogs: Computational Identification and Experimental Validation of New miRNA-mRNA Regulation in hiPSC-CMs.</pubmed_title><pmcid>PMC8962266</pmcid><funding_grant_id>00.219.2013</funding_grant_id><funding_grant_id>1501/8-2</funding_grant_id><pubmed_authors>Dieterich C</pubmed_authors><pubmed_authors>Britto-Borges T</pubmed_authors><pubmed_authors>Eschenbach J</pubmed_authors><pubmed_authors>Bencun M</pubmed_authors></additional><is_claimable>false</is_claimable><name>New Tricks with Old Dogs: Computational Identification and Experimental Validation of New miRNA-mRNA Regulation in hiPSC-CMs.</name><description>Cardiovascular disease is still the leading cause of morbidity and mortality worldwide. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have become a valuable widespread in vitro model to study cardiac disease. Herein, we employ the hiPSC-CM model to identify novel miRNA-mRNA interaction partners during cardiac differentiation and β-adrenergic stress. Whole transcriptome and small RNA sequencing data were combined to identify novel miRNA-mRNA interactions. Briefly, mRNA and miRNA expression profiles were integrated with miRNA target predictions to identify significant statistical dependencies between a miRNA and its candidate target set. We show by experimental validation that our approach discriminates true from false miRNA target predictions. Thereby, we identified</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-04-08T17:52:25.027Z</modification><creation>2025-04-04T23:15:30.323Z</creation></dates><accession>S-EPMC8962266</accession><cross_references><pubmed>35203600</pubmed><doi>10.3390/biomedicines10020391</doi></cross_references></HashMap>