Hanna Eberl
Wuerzburg, BY, Germany
Last Updated: 09/26/2026
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Found 8 publications
Peroxisomal catalase and plasmalogen biosynthesis protect from oxidative stress in Barth syndrome cardiomyopathy.
Journal: Basic research in cardiology
Published: November 25, 2025
RBM20 variants disrupt Ca2+ handling and metabolism in dilated and non-compaction cardiomyopathy stem cell models.
Journal: Signal transduction and targeted therapy
Published: July 01, 2025
Enhancing KLF15 activity in cardiomyocytes: a novel approach to prevent pathological reprogramming and fibrosis via nuclease-deficient dCas9VPR.
Journal: Signal transduction and targeted therapy
Published: December 10, 2024
Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation.
Journal: Stem cell research
Published: February 26, 2024
Generation of an RBM20-mutation-associated left-ventricular non-compaction cardiomyopathy iPSC line (UMGi255-A) into a DCM genetic background to investigate monogenetic cardiomyopathies.
Journal: Stem cell research
Published: July 27, 2023
Activation of the integrated stress response rewires cardiac metabolism in Barth syndrome.
Journal: Basic research in cardiology
Published: February 14, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026