(Q35637803)

English

Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population

scientific article published on 7 February 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

0 references

Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Catherine Boileau

0 references

author name string

J Wipff

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Y Allanore

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

A Kahan

3

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

O Meyer

4

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

L Mouthon

5

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

L Guillevin

6

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

C Pierlot

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

E Glikmans

8

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

T Bardin

9

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

C Boileau

10

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

F Cornélis

11

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

P Dieudé

12

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

language of work or name

0 references

publication date

7 February 2006

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Annals of the Rheumatic Diseases

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

65

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

1230-1232

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Altered B lymphocyte function induces systemic autoimmunity in systemic sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Is systemic sclerosis an antigen-driven T cell disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Protein tyrosine phosphorylation in T cell signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

12 July 2018

Lack of association between ankylosing spondylitis and a functional polymorphism of PTPN22 proposed as a general susceptibility marker for autoimmunity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

25 September 2018

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

25 September 2018

No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

25 September 2018

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1798267

25 September 2018

Scleroderma (systemic sclerosis): classification, subsets and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16464986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenic role of autoantibodies to nuclear autoantigens in systemic sclerosis (scleroderma)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16464986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/ARD.2005.048181

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

ResearchGate publication ID

0 references

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