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 variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.

BMJ (Clinical research ed.) - 30 Oct 1999

Gabolde M, Guilloud-Bataille M, Feingold J, Besmond C

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Carrier Proteins
Share to Cohort Studies
Share to Collectins
Share to Cystic Fibrosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forced Expiratory Volume

Share to Homozygote

Share to Respiration Disorders

Share to Vital Capacity

Source

Open in PubMed Open full text

Identifiers

PMID: 10541506
DOI: 10.1136/bmj.319.7218.1166
PMCID: PMC28266

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.PMID 10541506Read ↗

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotypeSemantic proximity Read ↗

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis.Semantic 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 deficiency and disease severity in non-cystic fibrosis bronchiectasis: a prospective studySemantic proximity Read ↗

Impaired pulmonary status in cystic fibrosis adults with two mutated MBL-2 alleles.Semantic proximity Read ↗

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

Modifier genes in cystic fibrosis lung disease.Semantic proximity Read ↗

The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.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 ↗

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

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

Mannose-binding lectin genotype and serum levels in patients with chronic and allergic pulmonary aspergillosis.Semantic proximity Read ↗

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