Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic polymorphisms of angiotensin system genes in congenital diaphragmatic hernia associated with persistent pulmonary hypertension.

Journal of pediatric surgery - 1 Mar 2004

Solari Valeria, Puri Prem

Abstract excerpt

BACKGROUND/PURPOSE: The renin-angiotensin system plays an important role in pulmonary artery remodelling. Several polymorphisms of genes encoding for components of the renin angiotensin system such as the angiotensin converting enzyme (ACE), the angiotensinogen (AGT) gene, and the angiotensin II type 1 receptor (ATIR) have been associated with the development of pulmonary hypertension. The aim of this study was...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Angiotensin II
Share to Angiotensinogen
Share to Hernia, Diaphragmatic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hernias, Diaphragmatic, Congenital

Share to Hypertension, Pulmonary

Share to Peptidyl-Dipeptidase A

Share to Receptors, Angiotensin

Share to Renin-Angiotensin System

Source

Identifiers

PMID: 15017542
DOI: 10.1016/j.jpedsurg.2003.11.008

Genes

ACE
AGT

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic polymorphisms of angiotensin system genes in congenital diaphragmatic hernia associated with persistent pulmonary hypertension.PMID 15017542Read ↗

Role of angiotensin-converting enzyme gene polymorphism in persistent pulmonary hypertension of the newborn.Semantic proximity Read ↗

Genetics of diaphragmatic hernia.Semantic proximity Read ↗

Relationship between angiotensin-converting enzyme gene polymorphism and respiratory distress syndrome in premature neonates.Semantic proximity Read ↗

Angiotensin-converting enzyme DD genotype in patients with primary pulmonary hypertension: increased frequency and association with preserved haemodynamics.Semantic proximity Read ↗

5'UTR repeat polymorphisms of the BMPR2 gene in children with pulmonary hypertension associated with congenital heart disease.Semantic proximity Read ↗

Angiotensin-converting enzyme gene insertion deletion (ACE I/D) polymorphism in Saudi children with congenital heart disease.Semantic proximity Read ↗

Assessment of insertion/deletion polymorphism of the angiotensin-converting enzyme gene in abdominal aortic aneurysm and inguinal hernia.Semantic proximity Read ↗

Polymorphism in the angiotensin II type 1 receptor (AGTR1) is associated with age at diagnosis in pulmonary arterial hypertension.Semantic proximity Read ↗

Etiologic and Genetic Factors in Congenital Diaphragmatic HerniaSemantic proximity Read ↗

ACE gene polymorphism in premature neonates with respiratory distress syndrome.Semantic proximity Read ↗

The association of angiotensin-converting enzyme gene polymorphism with respiratory distress syndrome in premature neonates.Semantic proximity Read ↗

Deletion allele of angiotensin-converting enzyme is associated with increased risk and severity of bronchopulmonary dysplasia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.