About
Contact & Profiles
A5030575776
Research Areas
- Pulmonary Hypertension Research and Treatments
- Medical Imaging and Pathology Studies
- Vascular Anomalies and Treatments
Stanford University
2020
Pulmonary arterial hypertension (PAH) is a fatal disease characterized by profound vascular remodeling in which pulmonary arteries narrow because of medial thickening and occlusion neointimal lesions, resulting elevated resistance right heart failure. Therapies targeting the neointima would represent significant advance PAH treatment; however, our understanding cellular events driving formation, molecular pathways that control them, remains limited. We comprehensively map stepwise robust,...
10.1161/circulationaha.120.045750
article
EN
Circulation
2020-08-14
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