A gene for primary pulmonary hypertension
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Localisation of the gene for familial primary pulmonary hypertension to chromosome 2q31-32;Nichols;Nat Genet,1997
2. Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene;Deng;Am J Hum Genet,2000
3. Heterozygous germline mutations in BMPR2, encoding a TGF-(β receptor, cause familial primary pulmonary hypertension;Nat Genet,2000
4. BMP2-induced apoptosis is mediated by activation of the TAK1-p38 kinase pathway that is negatively regulated by Smad6;Kimura;J Biol Chem,2000
5. Antiproliferative effects of recombinant human bone morphogenetic protein-2 on human tumor colony-forming units;Soda;Anticancer Drugs,1998
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1. The Metabolic Theory of Pulmonary Arterial Hypertension;Circulation Research;2014-06-20
2. Involvement of the bone morphogenetic protein system in endothelin- and aldosterone-induced cell proliferation of pulmonary arterial smooth muscle cells isolated from human patients with pulmonary arterial hypertension;Hypertension Research;2010-02-26
3. Multiple Endocrine Regulation by Bone Morphogenetic Protein System;Endocrine Journal;2010
4. Pulmonary Hypertension and Lung Transplantation;Current Hypertension Reviews;2008-02-01
5. Characterization of the Bone Morphogenetic Protein (BMP) System in Human Pulmonary Arterial Smooth Muscle Cells Isolated from a Sporadic Case of Primary Pulmonary Hypertension: Roles of BMP Type IB Receptor (Activin Receptor-Like Kinase-6) in the Mitotic Action;Endocrinology;2004-09-01
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