<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>71(4)</volume><submitter>Handoh T</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Dilated cardiomyopathy (DCM) is one of the leading causes of heart failure. To date, 48 genes are known to be associated with DCM. Telethonin, encoded by the &lt;i>TCAP&lt;/i> gene, is a Z-disk protein that composes cytoskeletal structures and facilitates various signaling pathways in cardiomyocytes. At least, six &lt;i>TCAP&lt;/i> variants have been found in patients with DCM. We sought to investigate the role of &lt;i>TCAP&lt;/i> in cardiac function using &lt;i>TCAP&lt;/i>-knockdown (KD) iPS cell (iPSC)-induced cardiomyocytes (CMs).&lt;h4>Methods &amp; results&lt;/h4>To investigate the role of &lt;i>TCAP&lt;/i> in cardiomyocytes, the &lt;i>TCAP&lt;/i> gene was knocked down in human iPS cells established from a healthy subject (201B7) using the CRISPR-Cas9 genome editing. The expressions of &lt;i>TCAP&lt;/i> mRNA and tel</pubmed_abstract><journal>Juntendo medical journal</journal><pagination>247-255</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12441175</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Knockdown of Telethonin Reduces Contractions and Provokes Aberrant Ca&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;-waves in Human iPS Cell-induced Cardiomyocytes.</pubmed_title><pmcid>PMC12441175</pmcid><pubmed_authors>Hori A</pubmed_authors><pubmed_authors>Ai T</pubmed_authors><pubmed_authors>Inaba H</pubmed_authors><pubmed_authors>Yamamoto H</pubmed_authors><pubmed_authors>Horiuchi Y</pubmed_authors><pubmed_authors>Tabe Y</pubmed_authors><pubmed_authors>Handoh T</pubmed_authors><pubmed_authors>Turker I</pubmed_authors><pubmed_authors>Miida T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Knockdown of Telethonin Reduces Contractions and Provokes Aberrant Ca&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;-waves in Human iPS Cell-induced Cardiomyocytes.</name><description>&lt;h4>Objectives&lt;/h4>Dilated cardiomyopathy (DCM) is one of the leading causes of heart failure. To date, 48 genes are known to be associated with DCM. Telethonin, encoded by the &lt;i>TCAP&lt;/i> gene, is a Z-disk protein that composes cytoskeletal structures and facilitates various signaling pathways in cardiomyocytes. At least, six &lt;i>TCAP&lt;/i> variants have been found in patients with DCM. We sought to investigate the role of &lt;i>TCAP&lt;/i> in cardiac function using &lt;i>TCAP&lt;/i>-knockdown (KD) iPS cell (iPSC)-induced cardiomyocytes (CMs).&lt;h4>Methods &amp; results&lt;/h4>To investigate the role of &lt;i>TCAP&lt;/i> in cardiomyocytes, the &lt;i>TCAP&lt;/i> gene was knocked down in human iPS cells established from a healthy subject (201B7) using the CRISPR-Cas9 genome editing. The expressions of &lt;i>TCAP&lt;/i> mRNA and tel</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-04-27T03:17:14.125Z</modification><creation>2026-04-27T03:11:10.475Z</creation></dates><accession>S-EPMC12441175</accession><cross_references><pubmed>40969822</pubmed><doi>10.14789/ejmj.JMJ24-0025-OA</doi></cross_references></HashMap>