Pulmonary arterial hypertension: insights from genetic studies. - Wikidata - awgldk - TriplyDB

Pulmonary arterial hypertension: insights from genetic studies.

Pulmonary arterial hypertension: insights from genetic studies.

http://www.wikidata.org/entity/Q35092474

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Epigenetic modulation as a therapeutic approach for pulmonary arterial hypertension Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension Abnormal trafficking of endogenously expressed BMPR2 mutant allelic products in patients with heritable pulmonary arterial hypertension Saudi Guidelines on the Diagnosis and Treatment of Pulmonary Hypertension: Genetics of pulmonary hypertension Pulmonary arterial hypertension in systemic lupus erythematosus: current status and future direction.A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.MicroRNAs: promising therapeutic targets for the treatment of pulmonary arterial hypertension.Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive.

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P2860

Pulmonary arterial hypertension: insights from genetic studies.

http://www.wikidata.org/entity/Q35092474

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Pulmonary arterial hypertension: insights from genetic studies.

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Pulmonary arterial hypertension: insights from genetic studies.

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Pulmonary arterial hypertension: insights from genetic studies.

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Pulmonary arterial hypertension: insights from genetic studies.

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Pulmonary arterial hypertension: insights from genetic studies.

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Pulmonary arterial hypertension: insights from genetic studies.

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PATS.201007-047MS

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Proceedings of the American Thoracic Society

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Pulmonary arterial hypertension: insights from genetic studies.

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James E Loyd

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P2860

Primary pulmonary hypertension. A national prospective study.

Gene expression in BMPR2 mutation carriers with and without evidence of pulmonary arterial hypertension suggests pathways relevant to disease penetrance

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

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

ACCF/AHA 2009 expert consensus document on pulmonary hypertension a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association developed in collaboration with the American Coll

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

A meta-analysis of trials of pulmonary hypertension: a clinical condition looking for drugs and research methodology.

Transcripts from a novel BMPR2 termination mutation escape nonsense mediated decay by downstream translation re-initiation: implications for treating pulmonary hypertension.

Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in females.

A meta-analysis of randomized controlled trials in pulmonary arterial hypertension

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154-157

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