1,026 results on '"Rabinovitch, Marlene"'
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2. Abstract 4134148: Reduced BMPR2 in Monocytes De-represses HERV-K and Sustains Inflammation in Pulmonary Arterial Hypertension
3. A computational growth and remodeling framework for adaptive and maladaptive pulmonary arterial hemodynamics
4. Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity
5. Life-saving effect of pulmonary surfactant in premature babies
6. Role of endothelial cells in pulmonary fibrosis via SREBP2 activation
7. Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension
8. Respiratory viruses and postoperative hemodynamics in patients with unrestrictive congenital cardiac communications: a prospective cohort study
9. Frataxin deficiency promotes endothelial senescence in pulmonary hypertension
10. Frataxin deficiency disrupts mitochondrial respiration and pulmonary endothelial cell function
11. Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program
12. MicroRNA‐483 amelioration of experimental pulmonary hypertension
13. Abstract 17218: CES1 Deficiency is Associated With Metabolic Reprograming and Endothelial Dysfunction in Pulmonary Arterial Hypertension
14. Hot topics in the mechanisms of pulmonary arterial hypertension disease: cancer‐like pathobiology, the role of the adventitia, systemic involvement, and right ventricular failure
15. Dysregulated Smooth Muscle Cell BMPR2–ARRB2 Axis Causes Pulmonary Hypertension
16. Dominant Role for Regulatory T Cells in Protecting Females Against Pulmonary Hypertension
17. KLF4 recruits SWI/SNF to increase chromatin accessibility and reprogram the endothelial enhancer landscape under laminar shear stress
18. Severe Pulmonary Arterial Hypertension Is Characterized by Increased Neutrophil Elastase and Relative Elafin Deficiency
19. Computational simulation-derived hemodynamic and biomechanical properties of the pulmonary arterial tree early in the course of ventricular septal defects
20. Are Senolytic Agents Guilty of Overkill or Inappropriate Age Discrimination?
21. Long-term miR-29b suppression reduces aneurysm formation in a Marfan mouse model.
22. Amphetamines promote mitochondrial dysfunction and DNA damage in pulmonary hypertension
23. Abstract 10270: High Shear Stress Decreases ERG Causing Endothelial to Mesenchymal Transition and Pulmonary Arterial Hypertension
24. Abstract 9727: Reduced Bmpr2 Causes a Decrease in Foxf1 That Links Unrepaired DNA Damage to Persistent Pulmonary Hypertension
25. Abstract 9501: Single-Cell Transcriptomic Analysis and Patient-Specific iPSCs Reveal Dysfunctional Coronary Arterial Endothelial Cells in Hypoplastic Left Heart Syndrome
26. Intrinsic Endocardial Defects Contribute to Hypoplastic Left Heart Syndrome
27. High Shear Stress Reduces ERG Causing Endothelial-Mesenchymal Transition and Pulmonary Arterial Hypertension
28. Single-Cell Imaging Maps Inflammatory Cell Subsets to Pulmonary Arterial Hypertension Vasculopathy
29. Landscape of cohesin-mediated chromatin loops in the human genome
30. BMPR2 Preserves Mitochondrial Function and DNA during Reoxygenation to Promote Endothelial Cell Survival and Reverse Pulmonary Hypertension
31. PPARγ Interaction with UBR5/ATMIN Promotes DNA Repair to Maintain Endothelial Homeostasis
32. Molecular Determinants of Lung Development
33. Evolution of hemodynamic forces in the pulmonary tree with progressively worsening pulmonary arterial hypertension in pediatric patients
34. Patient-Specific iPSC-Derived Endothelial Cells Uncover Pathways that Protect against Pulmonary Hypertension in BMPR2 Mutation Carriers
35. Relation of Cytokine Profile to Clinical and Hemodynamic Features in Young Patients With Congenital Heart Disease and Pulmonary Hypertension
36. Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension
37. Conditional and Targeted Overexpression of Vascular Chymase Causes Hypertension in Transgenic Mice
38. Abstract 15092: The Yin-yang of Bmpr2 and Ces1 in the Pulmonary Endothelium Aad Its Role in Pulmonary Arterial Hypertension
39. Abstract 12937: Single-cell Transcriptomic Analysis Reveals Developmentally Impaired Endocardial Population in Hypoplastic Left Heart Syndrome
40. Patient-Specific Induced Pluripotent Stem Cells Implicate Intrinsic Impaired Contractility in Hypoplastic Left Heart Syndrome
41. Regulation of Tenascin-C, a Vascular Smooth Muscle Cell Survival Factor That Interacts with the α vβ 3 Integrin to Promote Epidermal Growth Factor Receptor Phosphorylation and Growth
42. A Computational Growth and Remodeling Framework for Adaptive and Maladaptive Pulmonary Arterial Hemodynamics
43. Pathology, Pathobiology and Pathophysiology of Pulmonary Arterial Hypertension
44. Phenotypically Silent Bone Morphogenetic Protein Receptor 2 Mutations Predispose Rats to Inflammation-Induced Pulmonary Arterial Hypertension by Enhancing the Risk for Neointimal Transformation
45. Inflammatory Basis of Pulmonary Arterial Hypertension: Implications for Perioperative and Critical Care Medicine
46. Discovery of Distinct Immune Phenotypes Using Machine Learning in Pulmonary Arterial Hypertension
47. Smooth Muscle Contact Drives Endothelial Regeneration by BMPR2-Notch1–Mediated Metabolic and Epigenetic Changes
48. The α 2A-Adrenergic Receptor ( ADRA2A) Modulates Susceptibility to Raynaud's Syndrome
49. Pulmonary Hypertension and the Extracellular Matrix
50. Single-Cell Imaging Maps Inflammatory Cell Subsets to Pulmonary Arterial Hypertension Vasculopathy
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