<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Toni LS</submitter><funding>NHLBI NIH HHS</funding><pagination>e0221519</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6716635</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(8)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To investigate the biologic relevance of cross-platform concordant changes in gene expression in intact human failing/hypertrophied ventricular myocardium undergoing reverse remodeling.&lt;h4>Background&lt;/h4>Information is lacking on genes and networks involved in remodeled human LVs, and in the associated investigative best practices.&lt;h4>Methods&lt;/h4>We measured mRNA expression in ventricular septal endomyocardial biopsies from 47 idiopathic dilated cardiomyopathy patients, at baseline and after 3-12 months of β-blocker treatment to effect left ventricular (LV) reverse remodeling as measured by ejection fraction (LVEF). Cross-platform gene expression change concordance was investigated in reverse remodeling Responders (R) and Nonresponders (NR) using 3 platforms (RT-qPCR, mi</pubmed_abstract><journal>PloS one</journal><pubmed_title>Sequential analysis of myocardial gene expression with phenotypic change: Use of cross-platform concordance to strengthen biologic relevance.</pubmed_title><pmcid>PMC6716635</pmcid><funding_grant_id>R01 HL071118</funding_grant_id><funding_grant_id>T32 HL007822</funding_grant_id><pubmed_authors>Minobe WA</pubmed_authors><pubmed_authors>Lowes BD</pubmed_authors><pubmed_authors>Toni LS</pubmed_authors><pubmed_authors>Schwisow JA</pubmed_authors><pubmed_authors>Rodriguez EM</pubmed_authors><pubmed_authors>Buttrick PM</pubmed_authors><pubmed_authors>Altman NL</pubmed_authors><pubmed_authors>Kao DP</pubmed_authors><pubmed_authors>Bristow MR</pubmed_authors><pubmed_authors>Carroll IA</pubmed_authors><pubmed_authors>Jones KL</pubmed_authors><pubmed_authors>Gilbert EM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequential analysis of myocardial gene expression with phenotypic change: Use of cross-platform concordance to strengthen biologic relevance.</name><description>&lt;h4>Objectives&lt;/h4>To investigate the biologic relevance of cross-platform concordant changes in gene expression in intact human failing/hypertrophied ventricular myocardium undergoing reverse remodeling.&lt;h4>Background&lt;/h4>Information is lacking on genes and networks involved in remodeled human LVs, and in the associated investigative best practices.&lt;h4>Methods&lt;/h4>We measured mRNA expression in ventricular septal endomyocardial biopsies from 47 idiopathic dilated cardiomyopathy patients, at baseline and after 3-12 months of β-blocker treatment to effect left ventricular (LV) reverse remodeling as measured by ejection fraction (LVEF). Cross-platform gene expression change concordance was investigated in reverse remodeling Responders (R) and Nonresponders (NR) using 3 platforms (RT-qPCR, mi</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-19T16:44:31.42Z</modification><creation>2019-09-24T07:05:47Z</creation></dates><accession>S-EPMC6716635</accession><cross_references><pubmed>31469842</pubmed><doi>10.1371/journal.pone.0221519</doi></cross_references></HashMap>