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

Novel Mutation in the Class II Transactivator Associated with Immunodeficiency and Autoimmunity.

Journal of clinical immunology - 1 Aug 2015

Ahmed Aisha, Reith Walter, Puck Jennifer M, Cheng Laurence E

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 CD4-Positive T-Lymphocytes
Share to Codon, Nonsense
Share to Consanguinity
Share to Granulocyte Colony-Stimulating Factor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to HLA-DR Antigens

Share to Immunoglobulins, Intravenous

Share to Pneumocystis carinii

Share to Trans-Activators

Source

Open in PubMed Open full text

Identifiers

PMID: 26271388
DOI: 10.1007/s10875-015-0183-z
PMCID: PMC5512707

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel Mutation in the Class II Transactivator Associated with Immunodeficiency and Autoimmunity.PMID 26271388Read ↗

A novel mutation in ORAI1 presenting with combined immunodeficiency and residual T-cell function.Semantic proximity Read ↗

Novel heterozygous mutation of RTEL1 in interstitial pneumonia with autoimmune feature.Semantic proximity Read ↗

Mutation in the TACI gene and autoimmune neutropenia: A case report.Semantic proximity Read ↗

Two novel mutations in ZAP70 gene that result in human immunodeficiency.Semantic proximity Read ↗

MHC class II-deficient combined immunodeficiency: a disease of gene regulation.Semantic proximity Read ↗

Expanding the spectrum of recombination-activating gene 1 deficiency: a family with early-onset autoimmunity.Semantic proximity Read ↗

Immunodeficiency Associated with a Nonsense Mutation of IKBKBSemantic proximity Read ↗

Immunodeficiency and genetic defects of pattern-recognition receptors.Semantic proximity Read ↗

Three in vivo promoter phenotypes in MHC class II deficient combined immunodeficiency.Semantic proximity Read ↗

Novel IFNGR1 Mutation in a Child with Mycobacterium avium Infection.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: TAP2. Disease: HLA class I deficiency.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: TAP2. Disease: HLA class I deficiency.Semantic proximity Read ↗

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