◀ Back to EPHB2

EPHB2 — ESR2

Text-mined interactions from Literome

Singh et al., J Neurosci 2000 (MAP Kinase Signaling System) : Interestingly, the transcriptionally inactive stereoisomer 17alpha-estradiol did elicit a strong induction of ERK phosphorylation, which, together with the inability of the ER-alpha- and ER-beta-selective ligands to elicit ERK phosphorylation, and of ICI 182,780 to block the actions of estradiol in ERKO cultures, supports the hypothesis that a novel, estradiol-sensitive and ICI-insensitive estrogen receptor may mediate 17beta-estradiol induced activation of ERK in the brain
de Jager et al., J Biol Chem 2001 : Egr-1 mRNA and protein were rapidly and strongly induced by estrogen in an estrogen receptor dependent manner via the extracellular signal regulated kinase, ERK1/2
Lim et al., Int J Mol Med 2004 (MAP Kinase Signaling System) : Western blot shows that the activation of JNK signaling pathway, but not p38 and ERK , is dependent on ERbeta through estrogen treatment and APP-C105 is also mediated through estrogen in activating MAPK signaling pathway
Vallejo et al., Mol Endocrinol 2005 : Here we report that the proliferative response of UIII rat uterine stromal cells to a short treatment with progestins requires active progesterone receptor (PR) and estrogen receptor beta (ERbeta) as well as a rapid and transient activation of Erk1-2 and Akt signaling
Liu et al., Toxicol Appl Pharmacol 2008 (Breast Neoplasms) : It is concluded that Cd, like estradiol, can cause rapid activation of ERK1/2 and AKT and that these signaling events are mediated by possible interaction with membrane ER alpha and GPR30, but not ER beta
Vicent et al., Mol Endocrinol 2010 : Rapid activation of Erk by progestins via an interaction of the progesterone receptor (PR) with the estrogen receptor is critical for transcriptional activation of the mouse mammary tumor virus ( MMTV ) promoter and other progesterone target genes
Jain et al., Nanomedicine (Lond) 2012 (MAP Kinase Signaling System) : Our findings demonstrate that in vitro cadmium containing QDs induce cellular proliferation, estrogen receptor a activation , and biphasic phosphorylation of AKT and ERK1/2 , comparable with 17ß-estradiol
Watson et al., Steroids 2012 (MAP Kinase Signaling System...) : Estrogen- and xenoestrogen induced ERK signaling in pituitary tumor cells involves estrogen receptor-a interactions with G protein-ai and caveolin I
Hashimoto et al., Evidence-based complementary and alternative medicine : eCAM 2012 : These results suggest that ginsenoside Rb1 protects PC12 cells from caspase-3 dependent apoptosis through stimulation of estrogen receptor with consequent activation of ERK1/2 and Akt and inhibition of SAPK/JNK and p38