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SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2

Circulation research, 2021-04, Vol.128 (9), p.1323-1326

2021

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MDM2-Mediated Ubiquitination of Angiotensin-Converting Enzyme 2 Contributes to the Development of Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2020-09, Vol.142 (12), p.1190-1204

2020

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mTOR Signaling in Pulmonary Vascular Disease: Pathogenic Role and Therapeutic Target

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2144

2021

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Cellular and Molecular Basis of Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2009-06, Vol.54 (1), p.S20-S31

2009

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Mechanisms of hybrid oligomer formation in the pathogenesis of combined Alzheimer's and Parkinson's diseases

PloS one, 2008-09, Vol.3 (9), p.e3135

2008

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PFKFB3-mediated endothelial glycolysis promotes pulmonary hypertension

Proceedings of the National Academy of Sciences - PNAS, 2019-07, Vol.116 (27), p.13394-13403

2019

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Differentially expressed plasma microRNAs and the potential regulatory function of Let-7b in chronic thromboembolic pulmonary hypertension

PloS one, 2014-06, Vol.9 (6), p.e101055-e101055

2014

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Risk factors and basic mechanisms of chronic thromboembolic pulmonary hypertension: a current understanding

The European respiratory journal, 2013-02, Vol.41 (2), p.462-468

2013

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Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung

PloS one, 2016-03, Vol.11 (3), p.e0150480-e0150480

2016

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Halofuginone, a promising drug for treatment of pulmonary hypertension

British journal of pharmacology, 2021-09, Vol.178 (17), p.3373-3394

2021

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Endothelial Notch1 in Pulmonary Hypertension: Friend or Foe?

Circulation research, 2019-01, Vol.124 (2), p.176-179

2019

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Inflammation, Growth Factors, and Pulmonary Vascular Remodeling

Journal of the American College of Cardiology, 2009-06, Vol.54 (1), p.S10-S19

2009

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Targeting ATP-Sensitive K + Channels to Treat Pulmonary Hypertension

American journal of respiratory cell and molecular biology, 2022-05, Vol.66 (5), p.476-478

2022

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Endothelial HIF-2α contributes to severe pulmonary hypertension due to endothelial-to-mesenchymal transition

American journal of physiology. Lung cellular and molecular physiology, 2018-02, Vol.314 (2), p.L256-L275

2018

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Nicotinamide Phosphoribosyltransferase Promotes Pulmonary Vascular Remodeling and Is a Therapeutic Target in Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2017-04, Vol.135 (16), p.1532-1546

2017

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Upregulation of Piezo1 (Piezo Type Mechanosensitive Ion Channel Component 1) Enhances the Intracellular Free Calcium in Pulmonary Arterial Smooth Muscle Cells From Idiopathic Pulmonary Arterial Hypertension Patients

Hypertension (Dallas, Tex. 1979), 2021-06, Vol.77 (6), p.1974-1989

2021

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Endothelial dysfunction in pulmonary arterial hypertension: an evolving landscape (2017 Grover Conference Series)

Pulmonary circulation, 2018-01, Vol.8 (1), p.1-17

2018

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NEDD9, a Hypoxia-upregulated Mediator for Pathogenic Platelet-endothelial Cell Interaction in Pulmonary Hypertension

American journal of respiratory and critical care medicine, 2021-06, Vol.203 (12), p.1455-1458

2021

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Persistent eNOS activation secondary to caveolin-1 deficiency induces pulmonary hypertension in mice and humans through PKG nitration

The Journal of clinical investigation, 2009-07, Vol.119 (7), p.2009-2018

2009

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Upregulated expression of STIM2, TRPC6, and Orai2 contributes to the transition of pulmonary arterial smooth muscle cells from a contractile to proliferative phenotype

American Journal of Physiology: Cell Physiology, 2015-04, Vol.308 (8), p.C581-C593

2015

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Revisiting the Role of KCNA5 in Pulmonary Arterial Hypertension

American journal of respiratory cell and molecular biology, 2023-08, Vol.69 (2), p.123-125

2023

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Pathophysiology and pathogenic mechanisms of pulmonary hypertension: role of membrane receptors, ion channels, and Ca2+ signaling

Physiological reviews, 2023-07, Vol.103 (3), p.1827-1897

2023

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Tetramethylpyrazine: A promising drug for the treatment of pulmonary hypertension

British journal of pharmacology, 2020-06, Vol.177 (12), p.2743-2764

2020

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KCNK3 Channel: A New Player in the Field of Pulmonary Vascular Disease

Circulation research, 2019-09, Vol.125 (7), p.696-698

2019

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SGLT inhibitors attenuate NO-dependent vascular relaxation in the pulmonary artery but not in the coronary artery

American journal of physiology. Lung cellular and molecular physiology, 2015-11, Vol.309 (9), p.L1027-L1036

2015

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SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2

MDM2-Mediated Ubiquitination of Angiotensin-Converting Enzyme 2 Contributes to the Development of Pulmonary Arterial Hypertension

mTOR Signaling in Pulmonary Vascular Disease: Pathogenic Role and Therapeutic Target

Cellular and Molecular Basis of Pulmonary Arterial Hypertension

Mechanisms of hybrid oligomer formation in the pathogenesis of combined Alzheimer's and Parkinson's diseases

PFKFB3-mediated endothelial glycolysis promotes pulmonary hypertension

Differentially expressed plasma microRNAs and the potential regulatory function of Let-7b in chronic thromboembolic pulmonary hypertension

Risk factors and basic mechanisms of chronic thromboembolic pulmonary hypertension: a current understanding

Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung

Halofuginone, a promising drug for treatment of pulmonary hypertension

Endothelial Notch1 in Pulmonary Hypertension: Friend or Foe?

Inflammation, Growth Factors, and Pulmonary Vascular Remodeling

Targeting ATP-Sensitive K + Channels to Treat Pulmonary Hypertension

Endothelial HIF-2α contributes to severe pulmonary hypertension due to endothelial-to-mesenchymal transition

Nicotinamide Phosphoribosyltransferase Promotes Pulmonary Vascular Remodeling and Is a Therapeutic Target in Pulmonary Arterial Hypertension

Upregulation of Piezo1 (Piezo Type Mechanosensitive Ion Channel Component 1) Enhances the Intracellular Free Calcium in Pulmonary Arterial Smooth Muscle Cells From Idiopathic Pulmonary Arterial Hypertension Patients

Endothelial dysfunction in pulmonary arterial hypertension: an evolving landscape (2017 Grover Conference Series)

NEDD9, a Hypoxia-upregulated Mediator for Pathogenic Platelet-endothelial Cell Interaction in Pulmonary Hypertension

Persistent eNOS activation secondary to caveolin-1 deficiency induces pulmonary hypertension in mice and humans through PKG nitration

Upregulated expression of STIM2, TRPC6, and Orai2 contributes to the transition of pulmonary arterial smooth muscle cells from a contractile to proliferative phenotype

Revisiting the Role of KCNA5 in Pulmonary Arterial Hypertension

Pathophysiology and pathogenic mechanisms of pulmonary hypertension: role of membrane receptors, ion channels, and Ca2+ signaling

Tetramethylpyrazine: A promising drug for the treatment of pulmonary hypertension

KCNK3 Channel: A New Player in the Field of Pulmonary Vascular Disease

SGLT inhibitors attenuate NO-dependent vascular relaxation in the pulmonary artery but not in the coronary artery

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