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 PRKAR2A

IGFBP1 — PRKAR2A

Text-mined interactions from Literome

Frost et al., Endocrinology 2000 : Conversely, a PKA inhibitor ( H-89 ) inhibited the ability of cAMP, but not IL-1beta to stimulate IGFBP-1 synthesis
Whitehouse et al., J Endocrinol 2002 : We have now investigated the responses to PKA activation and inhibition of PP1/2A and used PTP inhibitors to examine the relationship between the morphological changes and enhanced steroid production
Woo et al., Eur J Neurosci 2002 (Synaptic Transmission) : Our data show that genetic inhibition of PKA impairs L-LTP by reducing PKA mediated suppression of PP1/2A
Yeagley et al., Mol Endocrinol 2005 : PKA and Dex also synergistically induced a minimal 3 x glucocorticoid response element promoter, but inhibited Dex induction of the mouse mammary tumor virus and IGF binding protein 1 promoters, even though PKA alone did not regulate these promoters
Suwanichkul et al., J Biol Chem 1993 (Carcinoma, Hepatocellular...) : In addition, cotransfection of the catalytic subunit of cAMP dependent protein kinase A (PKA) with the native 1205-bp IGFBP-1 promoter construct stimulated IGFBP-1 promoter activity 3.9-fold, but the TAGCA mutation decreased by 73 % the ability of PKA to stimulate IGFBP-1 promoter activity above control levels