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  1. Cardiomyocyte maturation alters molecular stress response capacities and determines cell survival upon mitochondrial dysfunction
  2. Cardiomyocyte hyperplasia and immaturity but not hypertrophy are characteristic features of patients with RASopathies
  3. Inhibition of mitochondrial respiration has fundamentally different effects on proliferation, cell survival and stress response in immature versus differentiated cardiomyocyte cell lines
  4. Dietary protein restriction throughout intrauterine and postnatal life results in potentially beneficial myocardial tissue remodeling in the adult mouse heart
  5. Impact of Intrauterine Growth Restriction on the Capillarisation of the Early Postnatal Rat Heart
  6. P448Dietary protein restriction throughout intrauterine development and postnatal life alters myocardial tissue composition but not left ventricular function in the adult mouse heart
  7. Molecular regulation of fetal growth and prenatal heart development
  8. Stress response of the hypoplastic mouse heart
  9. Preserved Heart Function after Left Ventricular Pressure Overload in Adult Mice Subjected to Neonatal Cardiac Hypoplasia
  10. Transcriptional profiling of regenerating embryonic mouse hearts
  11. Embryonic cardiomyocytes can orchestrate various cell protective mechanisms to survive mitochondrial stress
  12. Activation of Peroxisome Proliferator–Activated Receptor-δ as Novel Therapeutic Strategy to Prevent In-Stent Restenosis and Stent ThrombosisHighlights
  13. Prenatal mTORC1 Inhibition causes Fetal Growth Restriction and Impairs Heart Development
  14. Neonatal Cardiac Hypoplasia Alters Postnatal Growth and Stress Response in the Murine Heart
  15. Impaired myocardial development resulting in neonatal cardiac hypoplasia alters postnatal growth and stress response in the heart
  16. P313Embryonic cardiomyocytes can orchestrate various cell protective mechanisms to survive metabolic stress
  17. Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
  18. Heart Development: Mitochondria in Command of Cardiomyocyte Differentiation
  19. Growth plasticity of the embryonic and fetal heart
  20. Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia
  21. Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development
  22. Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction
  23. Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene
  24. The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
  25. Corrigendum: Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
  26. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
  27. Identification of the human ortholog of the t-complex-encoded protein TCTE3 and evaluation as a candidate gene for primary ciliary dyskinesia
  28. 3-D Imaging of Biomedical Samples