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 Haplotype TGGAG in the ABCA3 Gene Increases the Risk of Respiratory Distress Syndrome in Preterm Infants in Southern China.

Pediatrics and neonatology - 1 Jun 2016

Tian Wenjun, Chen Xiuqi, Qin Huijuan, Wei Qiufen, Zhang Shuying, Tang Shangying, Liao Liangrong, Zhang Yanming, Chen Yujun

Abstract excerpt

BACKGROUND: Rare mutations in the ATP-binding cassette (ABC) transporter A3 (ABCA3) gene are associated with neonatal respiratory distress syndrome (RDS). The contribution of common single nucleotide polymorphisms (SNPs) to preterm RDS differs between ethnicities and remains unclear in Chinese infants. This study evaluated whether common SNPs and consequent haplotypes increase susceptibility to RDS in a...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to ATP-Binding Cassette Transporters

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Infant, Newborn

Share to Infant, Premature

Share to Real-Time Polymerase Chain Reaction

Share to Respiratory Distress Syndrome, Newborn

Source

Identifiers

PMID: 26522252
DOI: 10.1016/j.pedneo.2015.09.002

Genes

ABCA3
MAF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Haplotype TGGAG in the ABCA3 Gene Increases the Risk of Respiratory Distress Syndrome in Preterm Infants in Southern China.PMID 26522252Read ↗

Polymorphism analysis of the ABCA3 gene: association with neonatal respiratory distress syndrome in preterm infants.Semantic proximity Read ↗

Evaluation of the Copy Number Variants and Single-Nucleotide Polymorphisms of ABCA3 in Newborns with Respiratory Distress Syndrome-A Pilot Study.Semantic proximity Read ↗

Haplotype analysis of ABCA3: association with respiratory distress in very premature infants.Semantic proximity Read ↗

Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.Semantic proximity Read ↗

A novel synonymous ABCA3 variant identified in a Chinese family with lethal neonatal respiratory failureSemantic proximity Read ↗

ABCA3 c.838C>T (p.Arg280Cys, R280C) and c.697C>T (p.Gln233Ter, Q233X, Q233*) as Causative Variants for RDS: a Review of the Literature and Family Case StudySemantic proximity Read ↗

Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population.Semantic proximity Read ↗

[Pulmonary surfactant associated gene variants in mixed ethnic population of Han and Zhuang].Semantic proximity Read ↗

Cumulative evidence of the genetic association between SP-B C1580T polymorphisms and risk of neonatal respiratory distress syndrome.Semantic proximity Read ↗

Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency.Semantic proximity Read ↗

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.Semantic proximity Read ↗

Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population.Semantic proximity Read ↗

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