(Q37390253)

20 August 2017

Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome (English)

1 reference

20 August 2017

Corinne Miceli-Richard

3

Corinne Miceli-Richard

0 references

Say Viengchareun

Say Viengchareun

4

0 references

Jorg Tost

Jorg Tost

17

0 references

Éric Hachulla

Eric Hachulla

14

0 references

Xavier Mariette

19

Xavier Mariette

1 reference

20 August 2017

18

Lindsey A Criswell

1 reference

20 August 2017

Christopher J Lessard

11

Christopher J Lessard

1 reference

20 August 2017

10

Judith Melki

1 reference

20 August 2017

Gaetane Nocturne

1

1 reference

20 August 2017

Saida Boudaoud

2

1 reference

20 August 2017

Corinne Miceli-Richard

3

1 reference

20 August 2017

Thierry Lazure

5

1 reference

20 August 2017

Joanne Nititham

6

1 reference

20 August 2017

Kimberly E Taylor

7

1 reference

20 August 2017

Averil Ma

8

1 reference

20 August 2017

Florence Busato

9

1 reference

20 August 2017

Kathy L Sivils

12

1 reference

20 August 2017

Jean-Jacques Dubost

13

1 reference

20 August 2017

Jacques Eric Gottenberg

15

1 reference

20 August 2017

Marc Lombès

16

1 reference

20 August 2017

language of work or name

English

0 references

publication date

24 October 2013

1 reference

20 August 2017

1 reference

20 August 2017

122

1 reference

20 August 2017

25

1 reference

20 August 2017

4068-4076

1 reference

Congenital B cell lymphocytosis explained by novel germline CARD11 mutations

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

A20: linking a complex regulator of ubiquitylation to immunity and human disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

A20 inactivation in ocular adnexal MALT lymphoma.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Promise and pitfalls of the Immunochip

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

MALT lymphoma: many roads lead to nuclear factor-κb activation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

TNFAIP3/A20 functions as a novel tumor suppressor gene in several subtypes of non-Hodgkin lymphomas

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Frequent inactivation of A20 in B-cell lymphomas

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

The NF-{kappa}B negative regulator TNFAIP3 (A20) is inactivated by somatic mutations and genomic deletions in marginal zone lymphomas.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Principal components analysis corrects for stratification in genome-wide association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

The risk of lymphoma development in autoimmune diseases: a meta-analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Classification criteria for Sjögren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Failure to regulate TNF-induced NF-kappaB and cell death responses in A20-deficient mice

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

STAT4is a genetic risk factor for systemic sclerosis having additive effects withIRF5on disease susceptibility and related pulmonary fibrosis

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3862283

10.1182/BLOOD-2013-05-503383

3 December 2018

Identifiers

DOI

1 reference

20 August 2017

1 reference

20 August 2017

1 reference