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1 ses, namely Raf, MEK (MAP kinase kinase) and ERK (MAP kinase).
2 L-4 and IL-13 also caused phosphorylation of ERK MAP kinase.
3 ETS proteins that are also phosphorylated by ERK MAP kinase.
4 ggesting that LIN-1 is directly regulated by ERK MAP kinase.
5 he interaction of betaarrs with clathrin and ERK MAP kinase.
6 cated in Wnt signalling and in activation of Erk MAP kinase.
7 independent of the activation of the bulk of ERK MAP kinase.
8 be associated with an increase in activated ERK-MAP kinase.
9 sis of docking interactions in a full-length ERK/MAP kinase.
10 ch is a protein kinase directly activated by Erk MAP kinases.
11 d for LPA-induced stimulation of the p38 and ERK MAP kinases.
12 ced phosphorylation of Smad1/5/8 and p38/Jnk/Erk MAP kinases.
13 here it mainly facilitates the activation of ERK MAP kinases.
14 thway linking receptor tyrosine kinases with Erk MAP kinases.
15 e induction is preceded by the activation of ERK MAP kinases.
16 dispersion, transiently activate the p42/p44 ERK/MAP kinases.
17 to play a key role in signal transduction by ERK/MAP kinases.
18 tions despite constitutive activation of the Erk/MAP kinases.
19 ctivation of extracellular signal regulated (Erk) MAP kinases.
20 results suggest a signaling pathway in which Erk MAP kinase activates the c-fos enhancer by direct ph
21 previously undescribed signaling pathway of ERK/MAP kinases activating calpain to destabilize cell-s
22 utocrine mediator of growth factor-dependent ERK MAP kinase activation and cell cycle progression.
23 l Gab2 as a limiting signaling component for Erk MAP kinase activation and terminal differentiation o
24 tributes strongly to phorbol ester (TPA) and Erk MAP kinase activation of the c-fos enhancer and that
26 induced RhoA/ROCK activation, but not p42/44 ERK MAP kinase activation, suggesting that Lbc is an int
29 of apoptosis protein 2) gene expression, and ERK/MAP kinase activation are all inhibited in TNF-treat
31 nt overall EGFR tyrosine phosphorylation and ERK/MAP kinase activation; however, phosphorylation of T
32 -regulated kinase/mitogen-activated protein (ERK/MAP) kinase activation, both of which have been impl
33 f focal adhesion kinase (FAK) and consequent ERK MAP kinase activity leading to Smad3 linker region p
34 f SDF-1alpha on T cells, including prolonged ERK MAP kinase activity, increased intracellular calcium
38 of PI3K signaling also blocked increases in ERK/MAP kinase activity associated with memory retrieval
40 scribe a versatile intracellular reporter of ERK/MAP kinase activity: a cDNA construct, pGFP.MBP, enc
43 B or HMGB-1 increased phosphorylation of the ERK MAP kinase and the p65 subunit of NF-kappaB and incr
44 -1(4H)-benzopyran-4-one], demonstrating that ERK MAP kinases and Akt are both required for EPO-induce
45 hways leading to activation of p38, JNK, and ERK MAP kinases and to generate reactive oxygen species.
46 ity phosphatase and a specific antagonist of ERK MAP kinases and we demonstrate that in somites Mkp3
48 on by Notch requires active signals from the Erk/MAP kinase and PI-3 kinase pathways downstream of Ra
49 ane-bound proteins in the dmPFC that include ERK/MAP kinase and the NMDA receptor subunits, GluN1 and
50 -Ha-ras and c-myc have high levels of active Erk/MAP kinase and their anchorage independent growth is
51 -regulated kinase/mitogen-activated protein (ERK/MAP) kinase and calpain (EC 3.4.22.17) in these proc
52 on and survival, including activation of the ERK/MAP kinases, and immediate-early induction of c-Jun
54 onarily conserved docking site that mediates ERK MAP kinase binding to substrates in multiple protein
56 xpression of KSR inhibited the activation of ERK MAP kinase by insulin, phorbol ester, or activated a
58 ticular, PEA-15 regulates the actions of the ERK MAP kinase cascade by binding to ERK and altering it
62 e Rap1A, but activates H-Ras, R-Ras, and the Erk/MAP kinase cascade under Ca2+ and DAG modulation.
67 ites in the hTERT promoter or suppression of ERK MAP kinase-dependent phosphorylation of ER81 rendere
69 CHO-K1) cells, uPA-binding to uPAR activates ERK/MAP kinase, even though these cells do not express t
70 expression can be mediated by SMAD, p38, and ERK/MAP kinase (extracellular signal-regulated kinase/mi
73 es, indicating that LIN-45, MEK-2, and MPK-1 ERK MAP kinase function in a predominantly linear signal
74 veral signal transduction pathways including ERK/MAP kinase have been implicated in memory retrieval,
75 ted forms of Mek (MAP kinase/Erk kinase) and Erk (MAP kinase) have been previously shown capable of i
76 olding complex is required for signaling via ERK MAP kinase in an efficient and specific manner upon
78 The differential contribution of p38 and ERK MAP kinases in mediating MKP-1 induction by differen
81 rc, Ras, Raf-1, Mek (MAP kinase kinase), and Erk (MAP kinase) in baculovirus-infected Sf9 insect cell
84 a molecular and pharmacologic assessment of Erk/MAP kinase, Jnk/SAP kinase, PI 3-kinase, protein kin
85 strointestinal smooth muscle which activates ERK MAP kinases leading to phosphorylation of caldesmon.
90 enetic proteins (BMPs) and activation of the ERK/MAP kinase (MAPK) pathway by growth factors have bee
92 ent, highlighting the importance of the MKP3-ERK-MAP kinase mediated feedback loop for cell specifica
98 fect on the ability of VHR to inactivate the ERK MAP kinases or to hydrolyze artificial substrates.
99 itors of these kinases but not inhibitors of ERK/MAP kinase or protein kinase C reduced heregulin-med
100 proteins, responsible for activation of the ERK MAP kinase pathway and a critical regulator of both
101 eta signaling through TACE activation by the Erk MAP kinase pathway and a strategy for evasion of tum
103 EK kinase is essential for activation of the Erk MAP kinase pathway during innate immune responses.
106 study suggest that targeting the RAGE or the ERK MAP kinase pathway may provide new therapeutic strat
109 TCR-induced calcium flux, activation of the ERK MAP kinase pathway, activation of the NF-kappaB tran
110 tein kinase Ctheta (PKCtheta) turning on the Erk MAP kinase pathway, but the biochemical mechanism re
120 ore regulated by both the mitogen-stimulated ERK/MAP kinase pathway and a PDK1-dependent pathway.
124 a suggested that sustained activation of the ERK/MAP kinase pathway promoted the autocrine secretion
125 n of both STAT transcription factors and the ERK/MAP kinase pathway, suggesting a mechanism for the o
126 ng the intracellular signaling involving the Erk/MAP kinase pathway, T cells with specificity for MHC
129 e data confirm the importance of the p38 and ERK MAP kinase pathways in macrophage activation by bact
132 in basic protein contains a single consensus ERK/MAP kinase phosphorylation motif (PRTP, where the th
133 on was associated with activation of p38 and ERK MAP kinases, phosphorylation of histone H3, and incr
134 by sequence-specific down-regulation of the ERK-MAP kinase phosphosignaling cascade in KRAS-driven c
135 vates extracellular signal-regulated kinase (ERK)-MAP kinases, reduced MAF mRNA in cells representing
136 striatum-enriched regulators of the Ras/Rap/ERK MAP kinase signal transduction cascade, matrix-enric
137 have described an important link between the ERK MAP kinase signaling cascade and the translational m
139 membrane TGF-alpha through activation of the Erk MAP kinase signaling cascade without the need for ne
140 imal activation of the canonical Ras/Raf/MEK/ERK Map kinase signaling cascade, likely because of PAK
142 , ECT-2, functions through the conserved RAS/ERK MAP kinase signaling pathway in the C. elegans germl
144 6 protein family, operates downstream of FGF/Erk MAP kinase signaling to regulate pluripotency and ce
146 resses EGF receptor signaling and downstream Erk MAP kinase signaling, as well as autocrine EGF recep
151 protein that integrates G protein and H-Ras/ERK/MAP kinase signaling pathways, thereby making it wel
153 -regulated kinase/mitogen-activated protein (ERK/MAP) kinase signaling but not on the immediate early
155 of Rho- dependent stress fibre formation by ERK-MAP kinase signalling contributes to the increased m
158 ay causes the phosphorylation of TGIF at two Erk MAP kinase sites, leading to TGIF stabilization and
159 However, TGF-beta stimulation also activates Erk MAP kinases through an undefined mechanism, albeit t
160 s driven in part by cAMP, which acts through Erk MAP kinase to initiate a cascade leading to modulati
163 role of beta-arrestins in the regulation of ERK MAP kinases, we examined the effect of beta-arrestin
164 via activation of p38 MAP kinase rather than ERK MAP kinase, which has more frequently been linked to
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