Genetics and mediators in pulmonary arterial hypertension - Wikidata - awgldk - TriplyDB

Genetics and mediators in pulmonary arterial hypertension

Genetics and mediators in pulmonary arterial hypertension

http://www.wikidata.org/entity/Q36752306

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Pulmonary arterial hypertension: a comparison between children and adults Gene expression in BMPR2 mutation carriers with and without evidence of pulmonary arterial hypertension suggests pathways relevant to disease penetrance A rapid and sensitive bioassay for the simultaneous measurement of multiple bone morphogenetic proteins. Identification and quantification of BMP4, BMP6 and BMP9 in bovine and human serum.Shorter survival in familial versus idiopathic pulmonary arterial hypertension is associated with hemodynamic markers of impaired right ventricular function Pulmonary arterial hypertension associated with systemic sclerosis.Neonatal hyperoxia causes pulmonary vascular disease and shortens life span in aging mice What patients and their relatives think about testing for BMPR2 Penetrance of pulmonary arterial hypertension is modulated by the expression of normal BMPR2 allele Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy.Genetic ablation of the BMPR2 gene in pulmonary endothelium is sufficient to predispose to pulmonary arterial hypertension.Systemic sclerosis-associated pulmonary arterial hypertension.Pulmonary Arterial Hypertension: Pathophysiology and Treatment.

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Genetics and mediators in pulmonary arterial hypertension

http://www.wikidata.org/entity/Q36752306

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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name

Genetics and mediators in pulmonary arterial hypertension

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Genetics and mediators in pulmonary arterial hypertension

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Genetics and mediators in pulmonary arterial hypertension

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J.CCM.2006.11.007

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Clinics in Chest Medicine

P1476

Genetics and mediators in pulmonary arterial hypertension

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P2093

Eric D Austin

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James E Loyd

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P2860

Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

Bone morphogenetic proteins, genetics and the pathophysiology of primary pulmonary hypertension

Mechanisms of TGF-beta signaling from cell membrane to the nucleus

Smad-dependent and Smad-independent pathways in TGF-beta family signalling

Gene expression patterns in the lungs of patients with primary pulmonary hypertension: a gene microarray analysis

Serotonin transporter overexpression is responsible for pulmonary artery smooth muscle hyperplasia in primary pulmonary hypertension

Clinical classification of pulmonary hypertension.

Primary pulmonary hypertension. A national prospective study.

Anorectic drugs and pulmonary hypertension from the bedside to the bench.

P304

43-57, vii-viii

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scholarly article

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10.1016/J.CCM.2006.11.007

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1

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2007-03-01T00:00:00Z

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17338927

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3740514

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