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Proceedings of the National Academy of Sciences of the United States of America|September 9, 2014
Essential role of sympathetic endothelin A receptors for adverse cardiac remodelingLorenz H Lehmann, Julia S Rostosky, Sebastian J Buss, et al.
The Journal of Molecular Diagnostics : JMD|July 25, 2025
Technical Advance, FoundationOne CDx and FoundationOne Heme Detect Epstein-Barr Virus with High Sensitivity and SpecificityJulius Honecker, Dirk Paffenholz, Julian Jungmann, et al.
Nature Communications|October 28, 2025
Endothelial RNF20 suppresses endothelial-to-mesenchymal transition and safeguards physiological angiocrine signaling to prevent congenital heart diseaseYanliang Dou, Nalan Tetik-Elsherbiny, Rui Gao, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 21, 2019
A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytesIbrahim El-Battrawy, Sebastian Albers, Lukas Cyganek, et al.
American Journal of Human Genetics|July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathyTobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
Circulation. Cardiovascular Genetics|March 11, 2017
Identification of Cadherin 2 (<i>CDH2</i>) Mutations in Arrhythmogenic Right Ventricular CardiomyopathyBongani M Mayosi, Maryam Fish, Gasnat Shaboodien, et al.
The Journal of Clinical Investigation|May 16, 2012
Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signalingMoritz Felcht, Robert Luck, Alexander Schering, et al.
Journal of Medical Genetics|October 2, 2015
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndromeRonja Hollstein, David A Parry, Lisa Nalbach, et al.
Circulation Research|November 2, 2016
Phosphodiesterase 2 Protects Against Catecholamine-Induced Arrhythmia and Preserves Contractile Function After Myocardial InfarctionChristiane Vettel, Marta Lindner, Matthias Dewenter, et al.
Frontiers in Cell and Developmental Biology|November 19, 2019
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived CardiomyocytesIbrahim El-Battrawy, Jonas Müller, Zhihan Zhao, et al.
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