BMPR2 mutations and endothelial dysfunction in pulmonary arterial hypertension (2017 Grover Conference Series)-Reference-Cited by-同舟云学术

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BMPR2 mutations and endothelial dysfunction in pulmonary arterial hypertension (2017 Grover Conference Series)

Published:2018-04 Issue:2 Volume:8 Page:1-12
ISSN:2045-8940
Container-title:Pulmonary Circulation
language:en
Short-container-title:Pulm. circ.

Author:

Frump Andrea¹,Prewitt Allison²,Caestecker Mark P.³

Affiliation:

1. Division of PulmonaryCritical Care, Sleep and Occupational MedicineIndiana University School of MedicineIndianapolisINUSA

2. MedpaceCincinnatiOHUSA

3. Division of Nephrology and HypertensionDepartment of MedicineVanderbilt University Medical centerNashvilleTNUSA

Funder

American Heart Association

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1177/2045894018765840

Reference88 articles.

1. Primary pulmonary hypertension;Runo JR;Lancet,2003

2. Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor‐II gene;Deng Z;Am J Hum Genet,2000

3. Heterozygous germline mutations in BMPR2, encoding a TGF‐beta receptor, cause familial primary pulmonary hypertension;Lane KB;Nat Genet,2000

4. BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta‐analysis;Evans JD;Lancet Respir Med,2016

5. Pulmonary arterial hypertension: a current perspective on established and emerging molecular genetic defects;Machado RD;Hum Mutat,2015

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4. The role of endothelial cells in pulmonary hypertension: old concepts and new science;Current Opinion in Physiology;2023-08

5. Unraveling the epigenetic landscape of pulmonary arterial hypertension: implications for personalized medicine development;Journal of Translational Medicine;2023-07-17

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