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

MBL2 gene polymorphisms increase the risk of adverse neurological outcome in preterm infants: a preliminary prospective study.

Pediatric research - 1 Nov 2014

Auriti Cinzia, Prencipe Giusi, Caravale Barbara, Coletti Maria Franca, Ronchetti Maria Paola, Piersigilli Fiammetta, Azzari Chiara, Di Ciommo Vincenzo M

Abstract excerpt

BACKGROUND: As described in animal models, the lectin-complement pathway is central to the propagation of ischemia-reperfusion injuries in many tissues, including the brain. Similarly, it might affect the genesis of brain damage in preterm infants. MBL2 gene single-nucleotide polymorphisms (SNPs), regulating mannose-binding lectin (MBL) serum levels, could predict the risk of adverse neurological outcome in these...

Read the complete abstract on PubMed

Topics

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

Share to Gestational Age
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Premature

Share to Longitudinal Studies

Share to Mannose-Binding Lectin

Share to Nervous System Diseases

Share to Neurologic Examination

Share to Risk Assessment

Source

Identifiers

PMID: 25119337
DOI: 10.1038/pr.2014.118

Genes

MBL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MBL2 gene polymorphisms increase the risk of adverse neurological outcome in preterm infants: a preliminary prospective study.PMID 25119337Read ↗

Mannose-binding lectin gene polymorphism and early neonatal outcome in preterm infants.Semantic proximity Read ↗

Evidence for an association between mannose-binding lectin 2 (MBL2) gene polymorphisms and pre-term birth.Semantic proximity Read ↗

Mannose-binding lectin genotypes are associated with shorter gestational age. An evolutionary advantage of low MBL production genotypes?Semantic proximity Read ↗

Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study.Semantic proximity Read ↗

Mannose-binding lectin haplotypes may be associated with cerebral palsy only after perinatal viral exposure.Semantic proximity Read ↗

Second-trimester plasma mannose-binding lectin levels and risk of preterm birth.Semantic proximity Read ↗

Association of polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants.Semantic proximity Read ↗

Association between mannose-binding lectin gene polymorphisms and necrotizing enterocolitis in preterm infants.Semantic proximity Read ↗

Mannose-binding lectin genotypes and pre-eclampsia: a case-control study.Semantic proximity Read ↗

Influence of MBL2 and NOS3 polymorphisms on spontaneous preterm birth in North East Brazil: genetics and preterm birth.Semantic proximity Read ↗

MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.Semantic proximity Read ↗

Mannose-binding lectin in term newborns and their mothers: genotypic and phenotypic relationship.Semantic proximity Read ↗

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