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

The role of plasminogen activator inhibitor-1 and angiotensin-converting enzyme gene polymorphisms in bronchopulmonary dysplasia.

Genetic testing and molecular biomarkers - 1 Oct 2010

Ince Deniz Anuk, Atac Fatma Belgin, Ozkiraz Servet, Dilmen Ugur, Gulcan Hande, Tarcan Aylin, Ozbek Namik

Abstract excerpt

BACKGROUND: Bronchopulmonary dysplasia (BPD) is a multifactorial disease of preterm infants that is characterized by airway injury, inflammation, and parencymal remodeling. Activation of the coagulation cascade leads to intraalveolar fibrin deposition in many inflammatory pulmonary disorders. Inc...

Read the complete abstract on PubMed

Topics

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

Share to Bronchopulmonary Dysplasia
Share to Infant, Newborn
Share to Infant, Premature

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Peptidyl-Dipeptidase A

Share to Plasminogen Activator Inhibitor 1

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Source

Open in PubMed Open full text

Identifiers

PMID: 20818980
DOI: 10.1089/gtmb.2010.0072
PMCID: PMC2957238

Genes

ACE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20818980-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of plasminogen activator inhibitor-1 and angiotensin-converting enzyme gene polymorphisms in bronchopulmonary dysplasia.PMID 20818980Read ↗

Lack of association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (915G/T) gene polymorphisms and bronchopulmonary dysplasia: a single-center study.Semantic proximity Read ↗

Dysplasia: A reviewSemantic proximity Read ↗

Role of Single Nucleotide Fibronectin Polymorphisms in Pathogenesis of Bronchopulmonary DysplasiaSemantic proximity Read ↗

Polymorphisms of fibronectin-1 (rs3796123; rs1968510; rs10202709; rs6725958; and rs35343655) Are Not Associated With Bronchopulmonary Dysplasia in Preterm Infants.Semantic proximity Read ↗

Pulmonary Hemorrhage in Premature Infants: Pathophysiology, Risk Factors and Clinical ManagementSemantic proximity Read ↗

Genetics of coagulation factors in acute lung injury.Semantic proximity Read ↗

Understanding the role of placental pathophysiology in the development of bronchopulmonary dysplasiaSemantic proximity Read ↗

Acute lung injury and the coagulation pathway: Potential role of gene polymorphisms in the protein C and fibrinolytic pathways.Semantic proximity Read ↗

Polymorphisms of fibronectin-1 (rs3796123; rs1968510; rs10202709; rs6725958; and rs35343655) are not associated with bronchopulmonary dysplasia in preterm infants.Semantic proximity Read ↗

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

Bronchopulmonary dysplasia and inflammatory biomarkers in the premature neonate.Semantic proximity Read ↗

Association of a FGFR-4 gene polymorphism with bronchopulmonary dysplasia and neonatal respiratory distress.Semantic proximity Read ↗

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