Investigation of theSLC22A4 gene (associated with rheumatoid arthritis in a Japanese population) in a United Kingdom population of rheumatoid arthritis patients-Reference-Cited by-同舟云学术

Investigation of theSLC22A4 gene (associated with rheumatoid arthritis in a Japanese population) in a United Kingdom population of rheumatoid arthritis patients

Published:2005 Issue:3 Volume:52 Page:752-758
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis Rheum

Author:

Barton Anne,Eyre Stephen,Bowes John,Ho Pauline,John Sally,Worthington Jane

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

Reference11 articles.

1. Genetic approaches to the investigation of rheumatoid arthritis

2. An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

3. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

4. A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

5. Functional variants of OCTN cation transporter genes are associated with Crohn disease

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