Bone morphogenetic protein receptor 2; Chronic thromboembolic pulmonary hypertension; Gene mutation
Indexed keywords
BERAPROST;
BONE MORPHOGENETIC PROTEIN 2;
SILDENAFIL;
WARFARIN;
ANTICOAGULANT AGENT;
ANTIHYPERTENSIVE AGENT;
BMPR2 PROTEIN, HUMAN;
BONE MORPHOGENETIC PROTEIN RECEPTOR 2;
Longterm follow-up of patients with pulmonary thromboembolism. Late prognosis and evolution of hemodynamic and respiratory data
Riedel M, Stanek V, Widimsky J, Prerovsky I (1982) Long-term follow-up of patients with pulmonary thromboembolism. Late prognosis and evolution of hemodynamic and respiratory data. Chest 81:151-158 (Pubitemid 12165545)
Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II
DOI 10.1164/rccm.200208-861OC
Runo JR, Vnencak-Jones CL, Prince M et al (2003) Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II. Am J Respir Crit Care Med 167:889-894 (Pubitemid 36801778)
BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives
Humbert M, Deng Z, Simonneau G et al (2002) BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives. Eur Respir J 20:518-523
BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease
DOI 10.1183/09031936.04.00018604
Roberts KE, McElroy JJ, Wong WP et al (2004) BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease. Eur Respir J 24:371-374 (Pubitemid 39232257)
Molecular genetics and clinical features of Chinese idiopathic and heritable pulmonary arterial hypertension patients
Liu D, Liu QQ, Eyries M et al (2012) Molecular genetics and clinical features of Chinese idiopathic and heritable pulmonary arterial hypertension patients. Eur Respir J 39:597-603
Incidence of chronic thromboembolic pulmonary hypertension after pulmonary embolism
Pengo V, Lensing AW, Prins MH et al (2004) Incidence of chronic thromboembolic pulmonary hypertension after pulmonary embolism. N Engl J Med 350:2257-2264
Dysfunctional Smad signaling contributes to abnormal smooth muscle cell proliferation in familial pulmonary arterial hypertension
DOI 10.1161/01.RES.0000166926.54293.68
Yang X, Long L, Southwood M et al (2005) Dysfunctional Smad signaling contributes to abnormal smooth muscle cell proliferation in familial pulmonary arterial hypertension. Circ Res 96:1053-1063 (Pubitemid 40791377)
Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension
Rajiv DM, Nung R, Carl A et al (2003) Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension. Hum Mol Genet 24:3277-3286