<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(9)</volume><submitter>Kang SM</submitter><pubmed_abstract>Hutchinson-Gilford Progeria Syndrome (HGPS) is an ultra-rare human premature aging disorder that precipitates death because of cardiac disease. Almost all cases of HGPS are caused by aberrant splicing of the &lt;i>LMNA&lt;/i> gene that results in the production of a mutant Lamin A protein termed progerin. In our previous study, treatment with Progerinin has been shown to reduce progerin expression and improve aging phenotypes in vitro and in vivo HGPS models. In this record, cardiac parameters (stroke volume (SV), ejection fraction (EF), fractional shortening (FS), etc.) were acquired in &lt;i>Lmna&lt;sup>WT/WT&lt;/sup>&lt;/i> and &lt;i>Lmna&lt;sup>G609G/WT&lt;/sup>&lt;/i> mice fed with either a vehicle diet or a Progerinin diet by echocardiography (from 38 weeks to 50 weeks at various ages), and then the cardiac funct</pubmed_abstract><journal>Cells</journal><pagination>1232</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10177486</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Progerinin, an Inhibitor of Progerin, Alleviates Cardiac Abnormalities in a Model Mouse of Hutchinson-Gilford Progeria Syndrome.</pubmed_title><pmcid>PMC10177486</pmcid><pubmed_authors>Kweon O</pubmed_authors><pubmed_authors>Seo S</pubmed_authors><pubmed_authors>Kim BH</pubmed_authors><pubmed_authors>Jo AH</pubmed_authors><pubmed_authors>Woo TG</pubmed_authors><pubmed_authors>Song EJ</pubmed_authors><pubmed_authors>Kang SM</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Oh GT</pubmed_authors><pubmed_authors>Park BJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Progerinin, an Inhibitor of Progerin, Alleviates Cardiac Abnormalities in a Model Mouse of Hutchinson-Gilford Progeria Syndrome.</name><description>Hutchinson-Gilford Progeria Syndrome (HGPS) is an ultra-rare human premature aging disorder that precipitates death because of cardiac disease. Almost all cases of HGPS are caused by aberrant splicing of the &lt;i>LMNA&lt;/i> gene that results in the production of a mutant Lamin A protein termed progerin. In our previous study, treatment with Progerinin has been shown to reduce progerin expression and improve aging phenotypes in vitro and in vivo HGPS models. In this record, cardiac parameters (stroke volume (SV), ejection fraction (EF), fractional shortening (FS), etc.) were acquired in &lt;i>Lmna&lt;sup>WT/WT&lt;/sup>&lt;/i> and &lt;i>Lmna&lt;sup>G609G/WT&lt;/sup>&lt;/i> mice fed with either a vehicle diet or a Progerinin diet by echocardiography (from 38 weeks to 50 weeks at various ages), and then the cardiac funct</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-21T22:42:55.584Z</modification><creation>2025-04-05T18:51:07.753Z</creation></dates><accession>S-EPMC10177486</accession><cross_references><pubmed>37174632</pubmed><doi>10.3390/cells12091232</doi></cross_references></HashMap>