1,010 results on '"Christoffels, Vincent"'
Search Results
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
4. Modeling the atrioventricular conduction axis using human pluripotent stem cell-derived cardiac assembloids
5. TBX3 is dynamically expressed in pancreatic organogenesis and fine-tunes regeneration
6. Mechanotransduction in Heart Development
7. Correction to: Fetal Tricuspid Valve Agenesis/Atresia: Testing Predictions of the Embryonic Etiology
8. Mechanotransduction in Heart Development
9. Regulatory element usage in healthy and failing human heart tissue
10. Neuregulin-1 enhances cell-cycle activity, delays cardiac fibrosis, and improves cardiac performance in rat pups with right ventricular pressure load
11. Equal force generation potential of trabecular and compact wall ventricular cardiomyocytes
12. Fetal Tricuspid Valve Agenesis/Atresia: Testing Predictions of the Embryonic Etiology
13. TBX2 specifies and maintains inner hair and supporting cell fate in the Organ of Corti
14. The Impact of Natriuretic Peptides on Heart Development, Homeostasis, and Disease
15. T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system
16. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
17. Sodium Glucose Cotransporter-2 Inhibitor Empagliflozin Reduces Infarct Size Independently of Sodium Glucose Cotransporter-2
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
20. Role of Genetic Variation in Transcriptional Regulatory Elements in Heart Rhythm
21. Combined genomic and proteomic approaches reveal DNA binding sites and interaction partners of TBX2 in the developing lung
22. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
23. Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction
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
30. Genetic Dissection of a Super Enhancer Controlling the Nppa-Nppb Cluster in the Heart
31. Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker Enhancer
32. Regulation of Vertebrate Conduction System Development
33. Cardiac Conduction System
34. Excessive trabeculations in noncompaction do not have the embryonic identity
35. TBX2-positive cells represent a multi-potent mesenchymal progenitor pool in the developing lung
36. Role of Genetic Variation in Transcriptional Regulatory Elements in Heart Rhythm.
37. Identification of Functional Variant Enhancers Associated With Atrial Fibrillation
38. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation
39. Development of the cardiac conduction system
40. Transcriptional regulation of the cardiac conduction system
41. Developmental Origin of the Cardiac Conduction System: Insight from Lineage Tracing
42. Structure and function of the Nppa–Nppb cluster locus during heart development and disease
43. Genetics of sinoatrial node function and heart rate disorders
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
48. An interactive three-dimensional digital atlas and quantitative database of human development
49. Conserved NPPB+ Border Zone Switches From MEF2- to AP-1–Driven Gene Program
50. Variation in a Left Ventricle–Specific Hand1 Enhancer Impairs GATA Transcription Factor Binding and Disrupts Conduction System Development and Function
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.