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

Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.

Genes and immunity - 1 Jan 2012

Janzi M, Melén E, Kull I, Wickman M, Hammarström L

Abstract excerpt

TACI (transmembrane activator and calcium modulator and cyclophilin ligand interactor) mutations seem to be associated with autoimmunity and common variable immunodeficiency in humans. Because of its role in immune responses, we investigated the association between TACI mutations and infection proneness/asthma symptoms in children. A total of 2372 children were genotyped for TACI mutations (I87N, C104R, S144X,...

Read the complete abstract on PubMed

Topics

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

Share to Immunoglobulin A
Share to Asthma
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Immunoglobulin G

Share to Prognosis

Share to Sweden

Share to Transmembrane Activator and CAML Interactor Protein

Source

Identifiers

PMID: 21850030
DOI: 10.1038/gene.2011.55

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.PMID 21850030Read ↗

Immunological characteristics and two novel mutations in TACI in a cohort of 28 pediatric patients with common variable immunodeficiency.Semantic proximity Read ↗

TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies.Semantic proximity Read ↗

A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.Semantic proximity Read ↗

TACI mutations and disease susceptibility in patients with common variable immunodeficiency.Semantic proximity Read ↗

Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes.Semantic proximity Read ↗

TACI mutation in common variable immunodeficiency and IgA deficiency.Semantic proximity Read ↗

The Coexistence of Asthma and Common Variable Immunodeficiency in a Patient with TNFRSF13B Gene Mutation.Semantic proximity Read ↗

TACI is mutant in common variable immunodeficiency and IgA deficiency.Semantic proximity Read ↗

Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.Semantic proximity Read ↗

Transmembrane activator and calcium-modulator and cyclophilin ligand interactor mutations in common variable immunodeficiency.Semantic proximity Read ↗

Heterozygous alterations of TNFRSF13B/TACI in tonsillar hypertrophy and sarcoidosis.Semantic proximity Read ↗

Phenotypic and clinical heterogeneity associated with monoallelic TNFRSF13B-A181E mutations in common variable immunodeficiency.Semantic proximity Read ↗

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