Differential drug response in pulmonary arterial hypertension: The potential for precision medicine
Abstract Pulmonary arterial hypertension (PAH) is a rare, complex, and deadly cardiopulmonary disease. It is characterized by changes in endothelial cell function and smooth muscle cell proliferation in the pulmonary arteries, causing persistent vasoconstriction, resulting in right heart hypertrophy...
| Автори: | , , , |
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| Формат: | Стаття |
| Мова: | English |
| Опубліковано: |
Wiley
2023-10-01
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| Серія: | Pulmonary Circulation |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1002/pul2.12304 |