We have a suspicion that you are an automated web bot software, not a real user. To keep our site fast for other users, we have slowed down this page. The slowdown will gradually disappear. If you think this is a mistake, please contact us at genome-www@soe.ucsc.edu. Also note that all data for hgGeneGraph can be obtained through our public MySQL server and all our software source code is available and can be installed locally onto your own computer. If you are unsure how to use these resources, do not hesitate to contact us.
UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

◀ Back to RELA

PIGR — RELA

Text-mined interactions from Literome

Ackermann et al., Immunology 2004 : In studies using human intestinal epithelial cells ( HT29 ), multiple inhibitors of the transcription factor nuclear factor-kappaB (NF-kappaB) , including a dominant negative IkappaBalpha-serine mutant, inhibited both IL-4- and IFN dependent increases in pIgR expression
Hinojosa et al., J Infect Dis 2009 (Inflammation...) : During pneumonia, aged mice had reduced levels of pIgR and PAFr and less NFkB activation , despite greater bacterial burden
Bruno et al., Immunol Invest 2010 : Induction of pIgR expression in HT-29 cells required NF-kappaB signaling but not MAPK signaling, in contrast to the requirement for both NF-kappaB and MAPK signaling for induction of pro-inflammatory genes
Bruno et al., Mucosal Immunol 2011 : Here, we examined the contributions of the RelA dependent classical and RelB dependent alternative pathways of NF-?B to pIgR regulation in the HT-29 human IEC line following stimulation with tumor necrosis factor (TNF), lipopolysaccharide ( LPS ; Toll-like receptor 4 (TLR4) ligand ), and polyinosinic : polycytidylic acid ( pIC ; TLR3 ligand )