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1. TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

2. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

3. Development of the Cardiac Conduction System

6. Mechanotransduction in Heart Development

16. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

18. Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms

19. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand

22. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice

24. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

25. HAND2 targets define a network of transcriptional regulators that compartmentalize the early limb bud mesenchyme.

26. TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy

27. Cardiomyocyte and endothelial cells play distinct roles in the tumor necrosis factor (TNF)-dependent atrial responses and increased atrial fibrillation vulnerability induced by endurance exercise training in mice

28. Contributors

29. Molecular therapies for bradyarrhythmias

31. Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker Enhancer

33. Cardiac Conduction System

36. Role of Genetic Variation in Transcriptional Regulatory Elements in Heart Rhythm.

38. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation

44. Ventricular function and biomarkers in relation to repair and pulmonary valve replacement for tetralogy of Fallot

45. Ventricular function and biomarkers in relation to repair and pulmonary valve replacement for tetralogy of Fallot

46. TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy

47. Ventricular function and biomarkers in relation to repair and pulmonary valve replacement for tetralogy of Fallot

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