glutathione pulmonary hypertension Ythdf2 promotes by suppressing Hmox1-dependent anti-inflammatory and antioxidant function in alveolar macrophages Pathological Mechanisms and Potential Therapeutic

Pathological Mechanisms and Potential Therapeutic Targets of Pulmonary Arterial Hypertension: A Review Frontiers Mitochondria in hypoxic pulmonary hypertension, roles and the potential targets Hyperuricemia and Hypoxic Pulmonary Hypertension: Pathogenic Links, Clinical Evidence, and Emerging Therapeutic Insights Cardiovascular Drugs and Therapy Springer Nature Link The progression of pulmonary arterial hypertension induced by monocrotaline is characterized by lung nitrosative and oxidative stress, and impaired pulmonary artery reactivity ScienceDirect Mechanisms of disease: pulmonary arterial hypertension Nature Reviews Cardiology Oxidative Stress and Antioxidative Therapy in Pulmonary Arterial Hypertension

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