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FOS — IRAK4
Text-mined interactions from Literome
Dolganiuc et al., Gastroenterology 2004
(Hepatitis C...) :
HCV core and NS3 induced interleukin (IL)-1 receptor associated kinase (
IRAK ) activity, phosphorylation of p38, extracellular regulated ( ERK ), and c-jun N-terminal ( JNK ) kinases and induced
AP-1 activation
Chandrasekar et al., J Biol Chem 2005
:
Src kinase inhibitors PP1 and PP2, phosphatidylinositol 3-kinase (PI3K) inhibitors wortmannin and LY294002, Akt inhibitor, the c-Jun N-terminal kinase (JNK) inhibitor SP600125, antisense JNK and dominant negative MyD88,
interleukin-1 receptor associated kinase ( IRAK)-1, IRAK4, and phosphatidylinositol 3-kinase expression all
attenuated IL-18 mediated
AP-1 binding and reporter activity, CXCL16 promoter-reporter activity, and CXCL16 expression
Merry et al., J Heart Lung Transplant 2010
(Lung Injury...) :
Lungs were assessed for vascular permeability, myeloperoxidase content, bronchoalveolar lavage inflammatory cell and cytokine/chemokine content, as well as nuclear translocation of nuclear factor kappaB (NFkappaB) and
activator protein-1 (AP-1) , and
interleukin-1 receptor associated kinase-1 ( IRAK-1 ) and stress activated protein kinase ( SAPK )
activation
Yang et al., J Ethnopharmacol 2013
:
In addition, the observed downregulation of
activator protein (AP)-1 and cAMP response element binding ( CREB ) was
due to the direct inhibition of
interleukin-1 receptor associated kinase ( IRAK)1 and IRAK4, which was also linked to the suppression of c-Jun N-terminal kinase (JNK) and p38