Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation. - Wikidata - wikimedia - TriplyDB

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

http://www.wikidata.org/entity/Q44096475

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Functional changes in pulmonary arterial endothelial cells associated with BMPR2 mutations Pathobiology of pulmonary arterial hypertension and right ventricular failure The genetics of pulmonary arterial hypertension Recent progress in understanding pediatric pulmonary hypertension Pulmonary arterial hypertension: an update A brief overview of mouse models of pulmonary arterial hypertension: problems and prospects.BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis Pediatric pulmonary arterial hypertension.Kidney dysfunction in patients with pulmonary arterial hypertension Development of pulmonary arterial hypertension in women: interplay of sex hormones and pulmonary vascular disease.Shorter survival in familial versus idiopathic pulmonary arterial hypertension is associated with hemodynamic markers of impaired right ventricular function Heritable forms of pulmonary arterial hypertension.Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertension.A novel BMPR2 mutation associated with pulmonary arterial hypertension in an octogenarian.BMPR2 mutation alters the lung macrophage endothelin-1 cascade in a mouse model and patients with heritable pulmonary artery hypertension.Chronic allergic inflammation causes vascular remodeling and pulmonary hypertension in BMPR2 hypomorph and wild-type mice Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn.Modification of hemodynamic and immune responses to exposure with a weak antigen by the expression of a hypomorphic BMPR2 gene Genetic counselling for pulmonary arterial hypertension: a matter of variable variability Pulmonary arterial hypertension: insights from genetic studies.Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations.The genetics of pulmonary arterial hypertension in the post-BMPR2 era.Associated pulmonary arterial hypertension in connective tissue diseases.A host-guest relationship in bone morphogenetic protein receptor-II defines specificity in ligand-receptor recognition.Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension.A Functional Variant rs6435156C > T in BMPR2 is Associated With Increased Risk of Chronic Obstructive Pulmonary Disease (COPD) in Southern Chinese Population Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects.2014 Guidelines of Taiwan Society of Cardiology (TSOC) for the Management of Pulmonary Arterial Hypertension.Bone morphogenetic protein signalling in heritable versus idiopathic pulmonary hypertension.Future perspectives for the treatment of pulmonary arterial hypertension.Genetics and genomics of pulmonary arterial hypertension.Genetics of pulmonary arterial hypertension.Correction of nonsense BMPR2 and SMAD9 mutations by ataluren in pulmonary arterial hypertension.Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension.Update in pulmonary hypertension 2008.Genotype-phenotype effects of Bmpr2 mutations on disease severity in mouse models of pulmonary hypertension.Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.Gene therapy for pulmonary hypertension: prospects and challenges.Pulmonary veno-occlusive disease: advances in clinical management and treatments.HIV infection and pulmonary arterial hypertension.

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P2860

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

http://www.wikidata.org/entity/Q44096475

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2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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name

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

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Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

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type

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Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

@en

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

@nl

prefLabel

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

@en

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

@nl

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American Journal of Respiratory and Critical Care Medicine

P1476

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation

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P2093

Azzedine Yaici

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Barbara Girerd

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Benjamin Sztrymf

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Florence Coulet

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P2860

Clinical classification of pulmonary hypertension.

Primary pulmonary hypertension. A national prospective study.

Pulmonary arterial hypertension in France: results from a national registry.

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension.

Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene.

Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.

Long-term response to calcium channel blockers in idiopathic pulmonary arterial hypertension.

Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension

Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family.

Cellular and molecular pathobiology of pulmonary arterial hypertension.

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