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Article

Absence of somatic MYD88 L265P mutations in patients with primary Sjogren's syndrome.

Genes and immunity - 1 Jan 2014

Voulgarelis M, Mavragani C P, Xu L, Treon S P, Moutsopoulos H M

Abstract excerpt

Sjogren's syndrome (SS) is a chronic autoimmune disorder with the highest risk for lymphoma development among all autoimmune diseases. In order to evaluate whether the presence of the recently described MYD88 L265P mutation in patients with Waldenström's macroglobulinemia (WM) is contributory to...

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Source

Identifiers

PMID: 24153350
DOI: 10.1038/gene.2013.54

Genes

MYD88

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24153350-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

Related research

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Absence of somatic MYD88 L265P mutations in patients with primary Sjogren's syndrome.PMID 24153350Read ↗

MYD88 L265P is a marker highly characteristic of, but not restricted to, Waldenström's macroglobulinemia.Semantic proximity Read ↗

MYD88 L265P in Waldenström macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction.Semantic proximity Read ↗

MYD88 mutation status does not impact overall survival in Waldenström macroglobulinemia.Semantic proximity Read ↗

[Lymphoproliferative disorders in Sjögren's syndrome].Semantic proximity Read ↗

Rare Circulating Cells in Familial Waldenström Macroglobulinemia Displaying the MYD88 L265P Mutation Are Enriched by Epstein-Barr Virus Immortalization.Semantic proximity Read ↗

L265P mutation of the MYD88 gene is frequent in Waldenström's macroglobulinemia and its absence in myeloma.Semantic proximity Read ↗

MYD88 (L265P) somatic mutation in marginal zone B-cell lymphoma.Semantic proximity Read ↗

MYD88 (L265P) mutation is an independent risk factor for progression in patients with IgM monoclonal gammopathy of undetermined significanceSemantic proximity Read ↗

Diagnostic Next-generation Sequencing Frequently Fails to Detect MYD88L265P in Waldenström MacroglobulinemiaSemantic proximity Read ↗

MYD88 L265P Somatic Mutation in IgM MGUSSemantic proximity Read ↗

An unusual case of cutaneous Waldenström macroglobulinemia with the MYD88 L265P mutation.Semantic proximity Read ↗

Detection of MYD88 L265P mutation by real-time allele-specific oligonucleotide polymerase chain reaction.Semantic proximity Read ↗

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