Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases (Q46368513)

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English	Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases	scientific article

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Europe PubMed Central

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15759012

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

title

Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases (English)

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Europe PubMed Central

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15759012

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

main subject

juvenile rheumatoid arthritis

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author

Erik Thorsby

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9

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Thorsby E

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Europe PubMed Central

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15759012

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21 December 2017

Tore K. Kvien

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3

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Kvien TK

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Europe PubMed Central

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15759012

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21 December 2017

Kirsten Muri Boberg

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Boberg KM

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15759012

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21 December 2017

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Viken MK

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1

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15759012

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http://europepmc.org/abstract/MED/15759012

Amundsen SS

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2

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15759012

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Gilboe IM

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5

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15759012

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Lilleby V

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6

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15759012

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21 December 2017

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Sollid LM

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7

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15759012

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21 December 2017

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Førre OT

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8

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15759012

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Smerdel A

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10

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15759012

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

Lie BA

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11

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15759012

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http://europepmc.org/abstract/MED/15759012

publication date

1 May 2005

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published in

Genes and Immunity

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

volume

6

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

issue

3

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15759012

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

page(s)

271-273

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21 December 2017

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http://europepmc.org/abstract/MED/15759012

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Clustering of autoimmune disease in parents of siblings from the Type 1 diabetes Warren repository

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21 January 2018

Comparative genetics of type 1 diabetes and autoimmune disease: common loci, common pathways?

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A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families

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21 January 2018

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

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

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

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The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

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

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The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritis

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Management of infantile gastroenteritis

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Primary sclerosing cholangitis: a review of its clinical features, cholangiography, and hepatic histology

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The common variants/multiple disease hypothesis of common complex genetic disorders

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

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Identifiers

DOI

10.1038/SJ.GENE.6364178

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Europe PubMed Central

PubMed publication ID

15759012

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15759012

PubMed publication ID

15759012

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15759012

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15759012

 

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