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ObjectiveThe p38 MAPK is important in the pathogenic immune response in rheumatoid arthritis (RA). The p38 molecule can be activated through phosphorylation on Thr180–Tyr182 by upstream MAPK kinases and via an alternative pathway through phosphorylation on Tyr323. We undertook this study to quantify the phosphorylation of Tyr323 p38 and of Thr180–Tyr182 p38 on T cells from healthy controls and patients...
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