Role of RUNX in autoimmune diseases linking rheumatoid arthritis, psoriasis and lupus
Open Access
- 1 January 2004
- journal article
- review article
- Published by Springer Science and Business Media LLC in Arthritis Research & Therapy
- Vol. 6 (4), 169-173
- https://doi.org/10.1186/ar1203
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Association of the PD‐1.3A allele of the PDCD1 gene in patients with rheumatoid arthritis negative for rheumatoid factor and the shared epitopeArthritis & Rheumatism, 2004
- A RUNX trio with a taste for autoimmunityNature Genetics, 2003
- RUNX transcription factors as key targets of TGF-β superfamily signalingCurrent Opinion in Genetics & Development, 2003
- Cbfβ interacts with Runx2 and has a critical role in bone developmentNature Genetics, 2002
- Differential Requirements for Runx Proteins in CD4 Repression and Epigenetic Silencing during T Lymphocyte DevelopmentCell, 2002
- A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humansNature Genetics, 2002
- In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesisBlood, 2002
- Raised serum vascular endothelial growth factor levels are associated with destructive change in inflammatory arthritisArthritis & Rheumatism, 2001
- Structural Analyses of DNA Recognition by the AML1/Runx-1 Runt Domain and Its Allosteric Control by CBFβCell, 2001
- Complement receptor (CR1) deficiency in erythrocytes from patients with systemic lupus erythematosus.The Journal of Experimental Medicine, 1982