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

Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children.

Pediatric pulmonology - 1 May 2020

Dogru Deniz, Polat Sanem E, Tan Çağman, Tezcan İlhan, Yalçın Sıddıka S, Utine Eda, Oğuz Berna, Yaz İsmail, Emiralioğlu Nagehan, Hızal Mina, Yalçın Ebru, Özçelik Uğur, Çağdaş Deniz, Kiper Nural

Abstract excerpt

BACKGROUND: Mannose-binding lectin (MBL) is a complement protein involved in the innate immune system, and is associated with some chronic respiratory diseases including noncystic fibrosis (non-CF) bronchiectasis in adults. The aim of this study was to investigate the frequency of MBL2 gene polymorphisms in children with non-CF bronchiectasis, and the effect of MBL deficiency on disease severity. METHODS: Fifty...

Read the complete abstract on PubMed

Topics

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

Share to Bronchiectasis
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Mannose-Binding Lectin

Share to Metabolism, Inborn Errors

Share to Respiratory Function Tests

Share to Severity of Illness Index

Source

Identifiers

PMID: 32119194
DOI: 10.1002/ppul.24711

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

Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children.PMID 32119194Read ↗

Mannose-binding lectin deficiency and disease severity in non-cystic fibrosis bronchiectasis: a prospective studySemantic proximity Read ↗

Impact of mannose-binding lectin insufficiency on the course of cystic fibrosis: A review and meta-analysis.Semantic proximity Read ↗

Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesia.Semantic proximity Read ↗

Complex two-gene modulation of lung disease severity in children with cystic fibrosis.Semantic proximity Read ↗

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

Genetic mannose binding lectin deficiency is associated with airway microbiota diversity and reduced exacerbation frequency in COPD.Semantic proximity Read ↗

Study of the effect of DNA polymorphisms in the mannose-binding lectin gene (MBL2) on disease severity in Slovak cystic fibrosis patients.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 genotype and serum levels in patients with chronic and allergic pulmonary aspergillosis.Semantic proximity Read ↗

Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency.Semantic proximity Read ↗

Mannose-binding lectin deficiency and respiratory tract infection.Semantic proximity Read ↗

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

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