Browse by author
Lookup NU author(s): Dr Kate Potter, Professor John IsaacsORCiD
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The introduction of anti-tumour necrosis factor (TNF) agents has greatly improved the treatment of rheumatoid arthritis; however, a significant proportion of patients fall to respond to therapy. We hypothesized that genes within the TNF receptor superfamily member 1 B signalling pathway contribute towards the observed variation in patient response. This was tested by genotyping 73 single-nucleotide polymorphisms (SNPs) from six candidate genes (DUSP1, HRB, IKBKAP, MAP3K1, MAP3K14 and TANK) in a large UK cohort of rheumatoid arthritis patients (n=642). Two SNPs [rs96844(MAP3K1) and rs4792847 (MAP3K14)] showed evidence of association (P
Author(s): Bowes JD, Potter C, Gibbons LJ, Hyrich K, Plant D, Morgan AW, Wilson AG, Isaacs JD, Worthington J, Barton A, BRAGGSS
Publication type: Article
Publication status: Published
Journal: Pharmacogenetics and Genomics
Year: 2009
Volume: 19
Issue: 4
Pages: 319-323
ISSN (print): 1744-6872
ISSN (electronic): 1744-6880
Publisher: Lippincott Williams & Wilkins
URL: http://dx.doi.org/10.1097/FPC.0b013e328328d51f
DOI: 10.1097/FPC.0b013e328328d51f
Altmetrics provided by Altmetric