All Stories

  1. Novel Tryptophan Hydroxylase Inhibitor TPT-001 Reverses PAH, Vascular Remodeling, and Proliferative-Proinflammatory Gene Expression
  2. ATP13A3 variants promote pulmonary arterial hypertension by disrupting polyamine transport
  3. Human umbilical cord mesenchymal stem cell-derived treatment of severe pulmonary arterial hypertension
  4. Pulmonary Arterial Hypertension and Consecutive Right Heart Failure Lead to Liver Fibrosis
  5. Circulating Interleukin-7 in Human Pulmonary Arterial Hypertension
  6. Letter by Legchenko et al Regarding Article, “Transcriptomic Analysis of Right Ventricular Remodeling in Two Rat Models of Pulmonary Hypertension: Identification and Validation of Epithelial-to-Mesenchymal Transition in Human Right Ventricular Failure”
  7. Soluble Receptor for Advanced Glycation End Products (sRAGE) Is a Sensitive Biomarker in Human Pulmonary Arterial Hypertension
  8. Emerging therapies for right ventricular dysfunction and failure
  9. Protein truncating mutations in ATP13A3 promote pulmonary arterial hypertension
  10. Trans-Right–Ventricle and Transpulmonary MicroRNA Gradients in Human Pulmonary Arterial Hypertension*
  11. Red blood cell-derived semaphorin 7A promotes thrombo-inflammation in myocardial ischemia-reperfusion injury through platelet GPIb
  12. Protein truncating mutations in ATP13A3 promote pulmonary arterial hypertension in mice
  13. The Adult Sprague-Dawley Sugen-Hypoxia Rat Is Still “the One:” A Model of Group 1 Pulmonary Hypertension: Reply to Le Cras and Abman
  14. PPARγ is a gatekeeper for extracellular matrix and vascular cell homeostasis
  15. Emphysema Is—at the Most—Only a Mild Phenotype in the Sugen/Hypoxia Rat Model of Pulmonary Arterial Hypertension
  16. Hypoxia drives cardiac miRNAs and inflammation in the right and left ventricle
  17. Chronic TGF-β1 Signaling in Pulmonary Arterial Hypertension Induces Sustained Canonical Smad3 Pathways in Vascular Smooth Muscle Cells
  18. PPARγ agonist pioglitazone reverses pulmonary hypertension and prevents right heart failure via fatty acid oxidation
  19. Transforming Growth Factor β1– and Bone Morphogenetic Protein 2/PPARγ–regulated MicroRNAs in Pulmonary Arterial Hypertension
  20. PPARγ Links BMP2 and TGFβ1 Pathways in Vascular Smooth Muscle Cells, Regulating Cell Proliferation and Glucose Metabolism
  21. Galectin-3 and aldosterone as potential tandem biomarkers in pulmonary arterial hypertension