Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene
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- 1 September 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (3) , 737-744
- https://doi.org/10.1086/303059
Abstract
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This publication has 36 references indexed in Scilit:
- Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanismsHuman Molecular Genetics, 2000
- TGF-β SIGNAL TRANSDUCTIONAnnual Review of Biochemistry, 1998
- Antiproliferatiye effects of recombinant human bone morphogenetic protein-2 on human tumor colony-forming unitsAnti-Cancer Drugs, 1998
- Monoclonal endothelial cell proliferation is present in primary but not secondary pulmonary hypertension.Journal of Clinical Investigation, 1998
- cDNA Cloning and Genomic Organization of the Mouse BMP Type II ReceptorBiochemical and Biophysical Research Communications, 1997
- Appetite-Suppressant Drugs and the Risk of Primary Pulmonary HypertensionNew England Journal of Medicine, 1996
- Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2Nature Genetics, 1996
- Immunologic Disturbances in Primary Pulmonary HypertensionSeminars in Respiratory and Critical Care Medicine, 1994
- Basic local alignment search toolJournal of Molecular Biology, 1990
- The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic DomainsScience, 1988