The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis (Q42949420)

From Wikidata

Jump to navigation Jump to search

scientific article published on January 2005

edit

Language	Label	Description	Also known as
English	The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis	scientific article published on January 2005

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

main subject

multiple sclerosis

0 references

author

Stacy J. Caillier

series ordinal

2

object named as

Stacy J Caillier

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

Lisa F Barcellos

series ordinal

6

object named as

Lisa F Barcellos

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

Jorge R. Oksenberg

series ordinal

7

object named as

Jorge R Oksenberg

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

Stephen L. Hauser

series ordinal

5

object named as

Stephen L Hauser

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

Ann B Begovich

series ordinal

1

object named as

Ann B Begovich

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

author name string

Heather C Alexander

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

Joanne M Penko

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

language of work or name

English

0 references

publication date

1 January 2005

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

volume

76

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

issue

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

page(s)

184-187

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

The genetics of complex autoimmune diseases: non-MHC susceptibility genes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Autoimmune disease: why and where it occurs.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Multiple sclerosis: a modifying influence of HLA class I genes in an HLA class II associated autoimmune disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

B cell repertoire diversity and clonal expansion in multiple sclerosis brain lesions

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Sequence requirements for association of protein-tyrosine phosphatase PEP with the Src homology 3 domain of inhibitory tyrosine protein kinase p50(csk)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Association of inhibitory tyrosine protein kinase p50csk with protein tyrosine phosphatase PEP in T cells and other hemopoietic cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

The future of genetic studies of complex human diseases

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

27 May 2018

Genotype‐based association test for general pedigrees: The genotype‐PDT

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

16 August 2018

Identification of autoantibodies associated with myelin damage in multiple sclerosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196423

retrieved

16 August 2018

Characterization of TCR-induced receptor-proximal signaling events negatively regulated by the protein tyrosine phosphatase PEP

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15580548

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic basis for clinical expression in multiple sclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15580548

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15580548

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15580548

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/427244

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

PMC publication ID

1196423

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

PubMed publication ID

15580548

1 reference

stated in

Europe PubMed Central

PMC publication ID

1196423

retrieved

11 November 2017

ResearchGate publication ID

8146446

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42949420&oldid=1974319835"