Pulmonary arterial hypertension: insights from genetic studies (Q35092474)

6 August 2017

title

Pulmonary arterial hypertension: insights from genetic studies (English)

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6 August 2017

main subject

arterial hypertension

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James E Loyd

1

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6 August 2017

publication date

1 May 2011

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Proceedings of the American Thoracic Society

6 August 2017

published in

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6 August 2017

volume

8

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6 August 2017

issue

2

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6 August 2017

page(s)

154-157

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Systematic review of trials using vasodilators in pulmonary arterial hypertension: why a new approach is needed

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

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Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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Penetrance of pulmonary arterial hypertension is modulated by the expression of normal BMPR2 allele

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

Primary pulmonary hypertension. A national prospective study

8 July 2018

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Survival in patients with idiopathic, familial, and anorexigen-associated pulmonary arterial hypertension in the modern management era.

8 July 2018

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Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension

27 September 2018

1 reference

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Pulmonary arterial hypertension: baseline characteristics from the REVEAL Registry.

27 September 2018

1 reference

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

27 September 2018

1 reference

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BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3131832

Familial primary pulmonary hypertension: clinical patterns

27 September 2018

1 reference

12 December 2020

Primary pulmonary hypertension in children may have a different genetic background than in adults

1 reference

12 December 2020

Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension

1 reference

12 December 2020

Synergistic heterozygosity for TGFbeta1 SNPs and BMPR2 mutations modulates the age at diagnosis and penetrance of familial pulmonary arterial hypertension

1 reference

12 December 2020

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32

1 reference

12 December 2020

Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32

1 reference

12 December 2020

10.1513/PATS.201007-047MS

Identifiers

DOI

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6 August 2017

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6 August 2017

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