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Article

Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertension.

European journal of human genetics : EJHG - 1 Jan 2007

Haberl Ines, Frei Klemens, Ramsebner Reinhard, Doberer Daniel, Petkov Ventzislav, Albinni Sulaima, Lang Irene, Lucas Trevor, Mosgoeller Wilhelm

Abstract excerpt

Pulmonary arterial hypertension is a progressive disease, characterised by increased proliferation of pulmonary artery smooth muscle cells, vasoconstriction and remodelling of the vascular wall leading to right heart failure and death. The idiopathic form is rare (idiopathic arterial primary hypertension (IPAH); formerly PPH, MIM# 178600). Our group correlated a deficiency in vasoactive intestinal peptide (VIP;...

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Identifiers

PMID: 17003842
DOI: 10.1038/sj.ejhg.5201711

Genes

VIP

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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