Andreas Perrot
Berlin, BE, Germany
Last Updated: 09/26/2026
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Found 23 publications
Human Genetics of Ventricular Septal Defect.
Journal: Advances in experimental medicine and biology
Published: June 17, 2024
Human Genetics of Defects of Situs.
Journal: Advances in experimental medicine and biology
Published: June 17, 2024
Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle.
Journal: Advances in experimental medicine and biology
Published: June 17, 2024
Nonsense mediated decay factor UPF3B is associated with cMyBP-C haploinsufficiency in hypertrophic cardiomyopathy patients.
Journal: Journal of molecular and cellular cardiology
Published: May 15, 2023
AQUA Mutant Protein Quantification of Endomyocardial Biopsy-Sized Samples From a Patient With Hypertrophic Cardiomyopathy.
Journal: Frontiers in cardiovascular medicine
Published: November 16, 2021
Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart.
Journal: Disease models & mechanisms
Published: April 28, 2020
Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy.
Journal: Revista portuguesa de cardiologia
Published: December 05, 2018
TIP30 counteracts cardiac hypertrophy and failure by inhibiting translational elongation.
Journal: EMBO molecular medicine
Published: November 01, 2018
Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy.
Journal: Frontiers in physiology
Published: January 23, 2018
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Journal: Journal of muscle research and cell motility
Published: June 22, 2017
Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes.
Journal: Journal of molecular and cellular cardiology
Published: April 09, 2017
Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.
Journal: European heart journal
Published: April 01, 2015
Last Updated: 09/26/2026