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

Low ficolin-2 levels in common variable immunodeficiency patients with bronchiectasis.

Clinical and experimental immunology - 1 Feb 2015

Metzger M-L, Michelfelder I, Goldacker S, Melkaoui K, Litzman J, Guzman D, Grimbacher B, Salzer U

Abstract excerpt

Common variable immunodeficiency (CVID) encompasses a heterogeneous group of antibody deficiencies characterized by susceptibility to recurrent infections and sequelae, including bronchiectasis. We investigated the relevance of the lectin complement pathway in CVID patients by analysing ficolin-2...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers
Share to Bronchiectasis
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Common Variable Immunodeficiency

Share to Ficolins

Share to Glycoproteins

Share to Lectins

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 25251245
DOI: 10.1111/cei.12459
PMCID: PMC4298403

Genes

FCN2
FCN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25251245-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Low ficolin-2 levels in common variable immunodeficiency patients with bronchiectasis.PMID 25251245Read ↗

Immunodeficiency Associated with <i>FCN3</i> Mutation and Ficolin-3 DeficiencySemantic proximity Read ↗

Association of Ficolin-2 Serum Levels and FCN2 Genetic Variants with Indian Visceral Leishmaniasis.Semantic proximity Read ↗

Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2Semantic proximity Read ↗

A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profileSemantic proximity Read ↗

Ficolin-2 defends against virulent Mycobacteria tuberculosis infection in vivo, and its insufficiency is associated with infection in humans.Semantic proximity Read ↗

L-ficolin (ficolin-2) insufficiency is associated with combined allergic and infectious respiratory disease in children.Semantic proximity Read ↗

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

Ficolin-3 in rheumatic fever and rheumatic heart disease.Semantic proximity Read ↗

Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.Semantic proximity Read ↗

Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency.Semantic proximity Read ↗

Common Variable Immunodeficiency Caused by FANC Mutations.Semantic proximity Read ↗

Reliable and rapid characterization of functional FCN2 gene variants reveals diverse geographical patterns.Semantic proximity Read ↗

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