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 polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants.

Genes and immunity - 1 Dec 2007

Hilgendorff A, Heidinger K, Pfeiffer A, Bohnert A, König I R, Ziegler A, Merz C, Frey G, Chakraborty T, Gortner L, Bein G

Abstract excerpt

Deficiency in the collectin mannose-binding lectin (MBL) increases the risk for pulmonary and systemic infections and its complications in children and adults. The aim of this prospective cohort study was to determine the genetic association of sequence variations within the MBL gene with systemic infections and pulmonary short- and long-term complications in preterm infants below 32 weeks gestational age (GA)....

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 Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Infant, Premature

Share to Mannose-Binding Lectin

Share to Promoter Regions, Genetic

Share to Respiratory Distress Syndrome, Newborn

Share to Respiratory Tract Infections

Source

Identifiers

PMID: 17898783
DOI: 10.1038/sj.gene.6364432

Genes

MBL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants.PMID 17898783Read ↗

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

Mannose-binding lectin genotype is associated with respiratory disease in young children: A multicenter cohort study.Semantic proximity Read ↗

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

Importance of mannose-binding lectin2 polymorphism (rs1800450) in infections in children.Semantic proximity Read ↗

Low mannose-binding lectin (MBL) levels in neonates with pneumonia and sepsis.Semantic proximity Read ↗

Biochemistry and genetics of mannan-binding lectin (MBL)Semantic proximity Read ↗

Mannose-binding lectin gene polymorphisms in infants with bronchiolitis and post-bronchiolitis wheezing.Semantic proximity Read ↗

Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms.Semantic proximity Read ↗

Clinical associations of complement-activating collectins, collectin-10, collectin-11 and mannose-binding lectin in preterm neonates.Semantic proximity Read ↗

Serum mannose-binding lectin (MBL) gene polymorphism and low MBL levels are associated with neonatal sepsis and pneumonia.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 and mannose-binding protein-associated serine protease 2 levels and infection in very-low-birth-weight infants.Semantic proximity Read ↗

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