Future Breakthroughs in the Genetics of Pulmonary Arterial Hypertension
Author:
Affiliation:
1. Department of MedicineUniversity of Cambridge School of Clinical MedicineAddenbrooke's and Papworth HospitalsCambridgeUnited Kingdom
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1086/674305
Reference11 articles.
1. Heterozygous germ‐line mutations in BMPR2, encoding a TGF‐receptor, cause familial primary pulmonary hypertension;International PPHC;Nat Genet,2000
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. Mutations of the TGF‐β type II receptor BMPR2 in pulmonary arterial hypertension;Machado RD;Hum Mutat,2006
4. The lysosomal inhibitor, chloroquine, increases cell surface BMPR‐II levels and restores BMP9 signalling in endothelial cells harbouring BMPR‐II mutations;Dunmore BJ;Hum Mol Genet,2013
5. Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation;Long L;Circ Res,2013
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Vasodilator responsiveness in idiopathic pulmonary arterial hypertension: identifying a distinct phenotype with distinct physiology and distinct prognosis;Pulmonary Circulation;2017-06
2. Pregnancy as a Possible Trigger for Heritable Pulmonary Arterial Hypertension;Pulmonary Circulation;2016-09
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