Genetic basis of pulmonary arterial hypertension
- 1 June 2004
- journal article
- review article
- Published by Elsevier BV in Journal of the American College of Cardiology
- Vol. 43 (12), S33-S39
- https://doi.org/10.1016/j.jacc.2004.02.028
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Autoantibodies against B23, a nucleolar phosphoprotein, occur in scleroderma and are associated with pulmonary hypertensionArthritis Care & Research, 2003
- Population Screening in the Age of Genomic MedicineNew England Journal of Medicine, 2003
- BMP signaling is required for septation of the outflow tract of the mammalian heartDevelopment, 2003
- Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseasesArthritis & Rheumatism, 2002
- Divergence and convergence of TGF‐β/BMP signalingJournal of Cellular Physiology, 2001
- Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta familyJournal of Medical Genetics, 2000
- Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II GeneAmerican Journal of Human Genetics, 2000
- Prophylactic thyroidectomy, based on direct genetic testing, in patients at risk for the multiple endocrine neoplasia type 2 syndromes*Experimental and Clinical Endocrinology & Diabetes, 1998
- Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32Nature Genetics, 1997
- Appetite-Suppressant Drugs and the Risk of Primary Pulmonary HypertensionNew England Journal of Medicine, 1996