(Q36727669)

English

Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis

scientific article published on 20 March 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

based on heuristic

inferred from title

author name string

María Carmen Cénit

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Ana Márquez

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Miguel Cordero-Coma

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Alejandro Fonollosa

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Victor Llorenç

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Joseba Artaraz

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

David Díaz Valle

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Ricardo Blanco

8

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Joaquín Cañal

9

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

David Salom

10

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

José Luis García Serrano

11

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Enrique de Ramón

12

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

María José del Rio

13

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Marina Begoña Gorroño-Echebarría

14

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

José Manuel Martín-Villa

15

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Blanca Molins

16

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Norberto Ortego-Centeno

17

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Javier Martín

18

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

publication date

20 March 2013

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Molecular Vision

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

19

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

638-643

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Genomics and the multifactorial nature of human autoimmune disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

A new look at immune privilege of the eye: dual role for the vision-related molecule retinoic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Autoimmune uveitis: the associated proinflammatory molecules and the search for immunoregulation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Current therapeutic approaches to autoimmune chronic uveitis in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Geoepidemiology: the environment and spondyloarthropathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Genotype analysis of polymorphisms in autoimmune susceptibility genes, CTLA-4 and PTPN22, in an acute anterior uveitis cohort.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Common genetic determinants of uveitis shared with other autoimmune disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

International Uveitis Study Group (IUSG): clinical classification of uveitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Identification of substrates of human protein-tyrosine phosphatase PTPN22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

The PTPN22 R620W polymorphism associates with RF positive rheumatoid arthritis in a dose-dependent manner but not with HLA-SE status

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

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=3611931

30 September 2017

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=3611931

30 September 2017

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=3611931

30 September 2017

Th1 and Th2 responses in pathogenesis and regulation of experimental autoimmune uveoretinitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Cooperative inhibition of T-cell antigen receptor signaling by a complex between a kinase and a phosphatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

Causes and frequency of blindness in patients with intraocular inflammatory disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

The natural history of uveitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

The association of the PTPN22 620W polymorphism with Behcet's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

30 September 2017

The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

5 September 2018

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

5 September 2018

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3611931

5 September 2018

PTPN22 gene polymorphism in Behçet's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23559857

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of HLA class II with pars planitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23559857

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-A29.2 subtype associated with birdshot retinochoroidopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23559857

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A locus on chromosome 9p predisposes to a specific disease manifestation, acute anterior uveitis, in ankylosing spondylitis, a genetically complex, multisystem, inflammatory disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23559857

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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