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

Common variable immunodeficiency and natural killer cell lymphopenia caused by Ets-binding site mutation in the IL-2 receptor γ (IL2RG) gene promoter.

The Journal of allergy and clinical immunology - 1 Mar 2016

Chandra Anita, Zhang Fang, Gilmour Kimberly C, Webster David, Plagnol Vincent, Kumararatne Dinakantha S, Burns Siobhan O, Nejentsev Sergey, Thrasher Adrian J

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 Binding Sites
Share to Common Variable Immunodeficiency
Share to Interleukin Receptor Common gamma Subunit

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Killer Cells, Natural

Share to Lymphopenia

Share to Promoter Regions, Genetic

Share to Protein Binding

Share to Proto-Oncogene Proteins c-ets

Source

Open in PubMed Open full text

Identifiers

PMID: 26525228
DOI: 10.1016/j.jaci.2015.08.049
PMCID: PMC4774944

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

Common variable immunodeficiency and natural killer cell lymphopenia caused by Ets-binding site mutation in the IL-2 receptor γ (IL2RG) gene promoter.PMID 26525228Read ↗

Analysis of Mutations in the IL2RG Gene in 2 Asian Infants With X-linked Severe Combined Immunodeficiency.Semantic proximity Read ↗

Case Report: Interleukin-2 Receptor Common Gamma Chain Defect Presented as a Hyper-IgE Syndrome.Semantic proximity Read ↗

Atypical immune phenotype in severe combined immunodeficiency patients with novel mutations in IL2RG and JAK3.Semantic proximity Read ↗

Novel mutation of IL2RG gene in a Korean boy with X-linked severe combined immunodeficiency.Semantic proximity Read ↗

The IL-2RG R328X nonsense mutation allows partial STAT-5 phosphorylation and defines a critical region involved in the leaky-SCID phenotype.Semantic proximity Read ↗

IL2RG-related immunodeficiencies: from SCID to atypical presentations.Semantic proximity Read ↗

Both integrated and differential regulation of components of the IL-2/IL-2 receptor system.Semantic proximity Read ↗

A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.Semantic proximity Read ↗

T+ NK+ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.Semantic proximity Read ↗

Somatic Reversion of a Novel IL2RG Mutation Resulting in Atypical X-Linked Combined Immunodeficiency.Semantic proximity Read ↗

Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency.Semantic proximity Read ↗

A novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene, in hyper-IgE syndrome.Semantic proximity Read ↗

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