Germline variation of TNFAIP3 in primary Sjögren's syndrome-associated lymphoma

Background and objectiveA germline and coding polymorphism (rs2230926) of TNFAIP3 (A20), a central gatekeeper of nuclear factor-kappa B (NF-kB) activation, was recently found associated with primary Sjögren's syndrome (pSS)-associated lymphoma in a French cohort. We aimed to replicate this asso...

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Veröffentlicht in:	Annals of the rheumatic diseases 2016-04, Vol.75 (4), p.780-783
Hauptverfasser:	Nocturne, Gaetane, Tarn, Jessica, Boudaoud, Saida, Locke, James, Miceli-Richard, Corinne, Hachulla, Eric, Dubost, Jean-Jacques, Bowman, Simon, Gottenberg, Jacques-Eric, Criswell, Lindsey A, Lessard, Christopher J, Sivils, Kathy L, Carapito, Raphael, Bahram, Siamak, Seror, Raphaèle, Ng, Wan-Fai, Mariette, Xavier
Format:	Artikel
Sprache:	eng
Schlagworte:	Blood & organ donations Case-Control Studies Cohort Studies DNA-Binding Proteins - genetics France Germ-Line Mutation - genetics Hodgkin Disease - genetics Humans Hypotheses Intracellular Signaling Peptides and Proteins - genetics Logistic Models Lymphoma Lymphoma - complications Lymphoma - genetics Lymphoma, B-Cell - genetics Meta-analysis Multivariate Analysis Mycosis Fungoides - genetics Nuclear Proteins - genetics Polymorphism, Single Nucleotide Sjogren's Syndrome - complications Sjogren's Syndrome - genetics Skin Neoplasms - genetics Tumor Necrosis Factor alpha-Induced Protein 3 United Kingdom White People - genetics
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