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

The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993.

Journal of immunology (Baltimore, Md. : 1950) - 1 Apr 2012

Vetrie David, Vořechovský Igor, Sideras Paschalis, Holland Jill, Davies Angela, Flinter Frances, Hammarström Lennart, Kinnon Christine, Levinsky Roland, Bobrow Martin, Smith C I Edvard, Bentley David R

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 Agammaglobulinaemia Tyrosine Kinase
Share to Agammaglobulinemia
Share to Consensus Sequence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

Share to History, 20th Century

Share to Proto-Oncogenes

Share to src-Family Kinases

Share to X Chromosome Inactivation

Source

Identifiers

PMID: 22442492

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

The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993.PMID 22442492Read ↗

[Gene diagnosis of X-linked agammaglobulinemia].Semantic proximity Read ↗

X-Linked AgammaglobulinemiaSemantic proximity Read ↗

Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia.Semantic proximity Read ↗

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivationSemantic proximity Read ↗

Mapping of the agammaglobulinemia tyrosine kinase gene on the mouse X chromosome with interspecific crosses.Semantic proximity Read ↗

X-linked agammaglobulinemia and other immunoglobulin deficiencies.Semantic proximity Read ↗

X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.Semantic proximity Read ↗

[Detection of Bruton's tyrosine kinase gene mutations and clinical analysis of 6 patients with X-linked agammaglobulinemia].Semantic proximity Read ↗

Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia.Semantic proximity Read ↗

Mapping of Zyx coding for zyxin in the rat and its exclusion as a candidate gene for lymphopenia.Semantic proximity Read ↗

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.Semantic proximity Read ↗

BTK gene mutation in two non-identical twins with X-linked agammaglobulinemia associated with polyarticular juvenile idiopathic arthritis.Semantic proximity Read ↗

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