Article

Discovery of <em>ETS1</em> as a New Gene Predisposing to Dilated Cardiomyopathy

2025-07-09

Abstract excerpt

<h4>Background: </h4> /Objectives: Dilated cardiomyopathy (DCM), defined as dilation and contractile dysfunction of the left or both cardiac ventricles, remains the most common category of primary myocardial disease worldwide. It is the most prevalent cause of chronic heart failure and the most common indication for cardiac transplantation in young subjects. Accumulating evidence increasingly highlights the substa...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 0a7b1a51-5d1b-5a20-8160-a8942a764c3b
DOI: 10.20944/preprints202507.0810.v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Discovery of <em>ETS1</em> as a New Gene Predisposing to Dilated CardiomyopathyDOI 10.20944/preprints202507.0810.v1Read

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.Semantic proximity Read

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.Semantic proximity Read

A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy.Semantic proximity Read

MYBPC3 (c.194CT) mutation-mediated RyR2 dysfunction contributes to pathogenic phenotypes of DCM revealed by hiPSC modelingSemantic proximity Read

HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.Semantic proximity Read

Homozygosity Mapping and Exome Sequencing Reveal <i>GATAD1</i> Mutation in Autosomal Recessive Dilated CardiomyopathySemantic proximity Read

A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient.Semantic proximity Read

Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing.Semantic proximity Read

GATA5 loss-of-function mutation in familial dilated cardiomyopathy.Semantic proximity Read

KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.Semantic proximity Read

Next-Generation Sequencing Screening Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese PatientsSemantic proximity Read

Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid modelsSemantic proximity Read