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

Association of the <italic>Glutathione S-Transferase M1</italic>-Null Genotype with Bronchopulmonary Dysplasia in Preterm Infants: A Brazilian Study.

Medical principles and practice : international journal of the Kuwait University, Health Science Centre - 1 Jan 2026

Nuevo Luana Vilches Cagnim, Piatto Vânia Belintani, Spessoto Luís Cesar Fava

Abstract excerpt

<p>Objectives: This study aimed to investigate whether the frequency of the Glutathione S-transferase M1 (GSTM1-null genotype) is associated with the development and/or severity of bronchopulmonary dysplasia (BPD) in premature newborns (PTNBs). MATERIALS AND METHODS: In this case-control study, 60 PTNBs with BPD and 42 PTNBs without BPD, of both sexes, were evaluated. DNA was extracted from peripheral blood...

Read the complete abstract on PubMed

Topics

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

Share to Brazil
Share to Bronchopulmonary Dysplasia

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Glutathione Transferase

Share to Infant, Newborn

Share to Infant, Premature

Source

Open in PubMed Open full text

Identifiers

PMID: 40716431
DOI: 10.1159/000547621
PMCID: PMC12503701

Genes

GSTM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of the <italic>Glutathione S-Transferase M1</italic>-Null Genotype with Bronchopulmonary Dysplasia in Preterm Infants: A Brazilian Study.PMID 40716431Read ↗

Molecular Approach of Oxidative Stress and Bronchopulmonary Dysplasia: Relationship of GSTM1 and GSTT1 Genes.Semantic proximity Read ↗

GSTM1 and GSTT1 gene polymorphisms as major risk factors for bronchopulmonary dysplasia in a Chinese Han population.Semantic proximity Read ↗

GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.Semantic proximity Read ↗

Oxidative Stress and Necrotizing Enterocolitis in Preterm Newborns: The Role of GSTM1 and GSTT1 Null Genotypes.Semantic proximity Read ↗

Association of glutathione-S-transferase-P1 (GST-P1) polymorphisms with bronchopulmonary dysplasia.Semantic proximity Read ↗

[Premature infants bronchopulmonary dysplasia: past and present].Semantic proximity Read ↗

Risk factors of bronchopulmonary dysplasia in premature infants under 32 weeks of gestation: A retrospective case-control studySemantic proximity Read ↗

[Assessing the impact of risk factors and polymorphisms GST genes on the development of bronchopulmonary dysplasia in premature infants].Semantic proximity Read ↗

Dysplasia: A reviewSemantic proximity Read ↗

TNF-238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population.Semantic proximity Read ↗

Surfactant protein B gene polymorphisms is associated with risk of bronchopulmonary dysplasia in Chinese Han population.Semantic proximity Read ↗

Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role.Semantic proximity Read ↗

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