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1 kinase interacting kinase-1, downstream from extracellular signal-regulated kinase.
2 osphorylation of phospholipase C gamma-1 and extracellular signal-regulated kinase.
3 r and activator of transcription 5, Akt, and extracellular signal-regulated kinase.
4 s and sAC is required for the acute phase of extracellular signal regulated kinase 1/2 activation tri
5 cardiovascular disease, is known to activate extracellular signal regulated kinases 1 and 2 (ERK1/2).
8 phorylation switch of IRS1/2 orchestrated by extracellular signal-regulated kinase 1 and 2 (ERK1/2) a
9 sults in the nuclear translocation of active extracellular signal-regulated kinase 1 and 2 (ERK1/2),
10 f BRAF/NRAS mutations and hyperactivation of extracellular signal-regulated kinase 1 and 2 (ERK1/2),
11 e to PDGF-BB, and reduced phosphorylation of extracellular signal-regulated kinase 1 and 2, Elk-1, p3
12 cell activation, as well as inflammasome and extracellular signal-regulated kinase 1 and 2-mediated n
13 in treatment and INSM1 inhibition suppressed extracellular signal-regulated kinase 1/2 (ERK1/2) activ
14 d transient IkappaBalpha phosphorylation and extracellular signal-regulated kinase 1/2 (ERK1/2) activ
15 ct resulted from cell-specific regulation of extracellular signal-regulated kinase 1/2 (ERK1/2) activ
16 that NPNT stimulates the phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) and p
17 Recent work suggested that the activity of extracellular signal-regulated kinase 1/2 (ERK1/2) is in
18 n target of rapamycin complex 1 (mTORC1) and extracellular signal-regulated kinase 1/2 (ERK1/2) pathw
19 pathways, including the NF-kappaB, AKT, and extracellular signal-regulated kinase 1/2 (ERK1/2) pathw
20 N-gamma, and the JAK1, STAT1, NF-kappaB, and extracellular signal-regulated kinase 1/2 (ERK1/2) pathw
21 inositol monophosphate (IP(1)) accumulation, extracellular signal-regulated kinase 1/2 (ERK1/2) phosp
22 s found to be dependent on activation of the extracellular signal-regulated kinase 1/2 (ERK1/2) signa
24 e (PI3-K), protein kinase C-zeta (PKC-zeta), extracellular signal-regulated kinase 1/2 (ERK1/2), NF-k
25 rotein kinase (MAPK) signaling, encompassing extracellular signal-regulated kinase 1/2 (ERK1/2), p38
26 the eIF4E upstream kinase) or inhibitors of extracellular signal-regulated kinase 1/2 (ERK1/2), the
27 iptolide binds to and activates p38alpha and extracellular signal-regulated kinase 1/2 (ERK1/2), whic
28 asmin generation, but instead is mediated by extracellular signal-regulated kinase 1/2 (ERK1/2)-regul
29 only combined treatment of mitogen-activated extracellular signal-regulated kinase 1/2 (MEK1/2) and S
31 f both intracellular Ca(2+) mobilization and extracellular signal-regulated kinase 1/2 activation, wh
32 C cells and resulted in potent inhibition of extracellular signal-regulated kinase 1/2 activation.
34 -mediated signalling pathway, including p38, extracellular signal-regulated kinase 1/2 and c-Jun N-te
35 ulated PgLPS-mediated phosphorylation of the extracellular signal-regulated kinase 1/2 and c-Jun N-te
36 to a series of downstream events, including extracellular signal-regulated kinase 1/2 and c-Jun N-te
38 cKL + FGF23 increased the phosphorylation of extracellular signal-regulated kinase 1/2 and induced Fg
39 hosphates) in some signaling events, such as extracellular signal-regulated kinase 1/2 and label free
40 cted with the LRP1/NMDA-R system to activate extracellular signal-regulated kinase 1/2 and promote ce
41 and was coupled with decreased expression of extracellular signal-regulated kinase 1/2 kinase signali
42 assays, and ChIP revealed that DDR2 acts via extracellular signal-regulated kinase 1/2 mitogen-activa
43 pling, betaarr recruitment, endocytosis, and extracellular signal-regulated kinase 1/2 mitogen-activa
44 that Ach upregulated TGFbetaRII through Src-extracellular signal-regulated kinase 1/2 pathway to pot
45 i) coupling as measured by cAMP response and extracellular signal-regulated kinase 1/2 phosphorylatio
46 urally distinct MEKi trametinib and elevated extracellular signal-regulated kinase 1/2 phosphorylatio
47 s down-regulated, followed by an increase in extracellular signal-regulated kinase 1/2 phosphorylatio
48 ells, Ptges expression was regulated through extracellular signal-regulated kinase 1/2 phosphorylatio
49 ray of mechanistic studies revealed impaired extracellular signal-regulated kinase 1/2 signaling in H
50 n-1-SYK-epidermal growth factor receptor-AKT/extracellular signal-regulated kinase 1/2 signaling path
51 inhibiting cAMP accumulation and activating extracellular signal-regulated kinase 1/2 signaling whil
52 n high glucose condition interferes with Src-extracellular signal-regulated kinase 1/2 signaling, res
53 ading to activation of MAPK kinase (MEK) and extracellular signal-regulated kinase 1/2 signaling; how
54 was transactivated by Src family kinases and extracellular signal-regulated kinase 1/2 was activated
55 nase p38 was enhanced and phosphorylation of extracellular signal-regulated kinase 1/2 was decreased
56 ayed rapid increases in activated STAT1/3/5, extracellular signal-regulated kinase 1/2, AKT, CREB, an
57 es and were associated with an activation of extracellular signal-regulated kinase 1/2, and ribosomal
58 r and activator of transcription 5, AKT, and extracellular signal-regulated kinase 1/2, determining i
59 ory effects, increased inhibition of phospho-extracellular signal-regulated kinase 1/2, increased mit
60 nt phosphorylation of the downstream kinases extracellular signal-regulated kinase 1/2, mitogen-activ
61 ey signaling intermediates protein kinase B, extracellular signal-regulated kinase 1/2, NF-kappaB, an
62 ng MMP-9 secretion through the activation of extracellular signal-regulated kinase 1/2, p38, phosphoi
63 down resulted in decreased levels of phospho-extracellular signal-regulated kinase 1/2, phospho-c-Jun
65 STAT3, which is significantly enhanced by an extracellular signal-regulated kinase 1/2-dependent mTOR
66 ed activation of cardiac fibroblasts through extracellular signal-regulated kinase 1/2-dependent phos
67 emic retinopathy selectively activates GPR81-extracellular signal-regulated kinase 1/2-Norrin signali
68 els of phosphorylated IkappaBalpha, Akt, and extracellular signal-regulated kinase 1/2; nuclear trans
69 carcinoma (HCT116) cells treated with H2O2, extracellular signal-regulated kinases 1 and 2 (ERK1/2)
70 Here, we show that sustained activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2)
71 ses 1 and 2 (MNK1 and MNK2) are activated by extracellular signal-regulated kinases 1 and 2 (ERK1/2)
72 activation of phosphoinositide 3-kinase and extracellular signal-regulated kinases 1 and 2 by Gbetag
74 ated kinase 1 (MSK1), a downstream target of extracellular signal-regulated kinases 1 and 2, and an i
75 ion of p38 mitogen-activated protein kinase, extracellular signal-regulated kinases 1 and 2, and Jun
76 a resulted in reduced phosphorylation of the extracellular signal-regulated kinases 1 and 2, enhanced
77 ethyl-D-aspartate receptors or activation of extracellular signal-regulated kinases 1 and 2, or block
78 nic ability, and invasiveness by suppressing extracellular signal-regulated kinases 1/2 (ERK1/2) and
79 eported mediator in vibratory urticaria, and extracellular signal-regulated kinases 1/2 activation wa
80 treated with necrotic bone showed increased extracellular signal-regulated kinases 1/2 and Ikappa ki
82 ase C, and phosphoinositide 3-kinase but not extracellular signal-regulated kinases 1/2 pathways, alo
83 oduction and produced enduring activation of extracellular signal-regulated kinases 1/2 phosphorylati
86 ation of mammalian target of rapamycin, AKT, extracellular signal-regulated kinases 1/2, phosphatase
87 tion while reducing fibroblast growth factor/extracellular signaling-regulated kinase 1/2 activity in
89 2) (COT, MAP3K8) kinase activates the MEK1/2-extracellular-signal regulated kinase 1/2 MAP kinase sig
90 ng alpha-MSH production via CB1R-induced and extracellular-signal-regulated kinase 1/2 activation- an
93 beta-arrestin recruitment and DHA-dependent extracellular-signal regulated kinase-1/2 (ERK1/2) signa
96 ind the nonphosphorylated (inactive) form of extracellular signal-regulated kinase 2 (ERK2) or its do
97 f miR-494 as a result of the inactivation of extracellular signal-regulated kinase 2 (ERK2), in turn
98 cents, phosphorylation of the trkB substrate extracellular signal-regulated kinase 42/44 (ERK42/44) i
99 hanistic studies revealed that activation of extracellular signal-regulated kinase 5 (ERK5) via upreg
100 thrombosis by increasing activation of MAPK extracellular signal-regulated kinase 5 (ERK5), a protei
101 gen-activated protein kinase kinase 5)-ERK5 (extracellular signal-regulated kinase 5) signaling and c
102 nflammatory molecules and activation of ERK (extracellular signal-regulated kinase) 5/p38 pathways.
103 that TRAF1 is required for solar UV-induced extracellular signal-regulated kinase-5 (ERK5) phosphory
105 -function variant-mediated Ca(2+) influx and extracellular signal-regulated kinase activation in HEK
106 reactive oxygen species production, and p38/extracellular signal-regulated kinase activation in mast
107 growth factor receptor signalling, including extracellular signal-regulated kinase activation, to dri
109 sympathetic nerves increase endothelial ERK (extracellular signal-regulated kinase) activity via adre
110 ct of each variant on the activation of ERK (extracellular signal-regulated kinase), AKT (protein kin
111 oncomitant down-regulation of phosphorylated extracellular signal-regulated kinase and myeloid cell l
112 orters, mRNAs, signaling (phosphorylation of extracellular signal-regulated kinase and phospholamban)
113 receptor 2AT4 and induced phosphorylation of extracellular signal-regulated kinases and p38 mitogen-a
115 extracellular signal-regulated kinase kinase-extracellular signal-regulated kinase) and S6K-RPS6 (rib
116 -fold, inactivated the key signaling protein extracellular signal-regulated kinase, and increased apo
117 ormation, possibly through protein kinase B, extracellular signal-regulated kinase, and NF-kappaB pat
118 nsducer and activator of transcription 5 and extracellular signal-regulated kinase, and transforms pa
119 ed B cells-p65, increased phosphorylation of extracellular-signal-regulated kinase, and reduced the e
120 inositol 1,4,5-triphosphate/protein kinase C/extracellular signal-regulated kinase) are major mediato
121 nsducer and activator of transcription 3 and extracellular signal-regulated kinase, as well as format
122 Finally, combined inhibition of the Raf/MAPK/extracellular signal-regulated kinase axis and eIF4E imp
124 and three mitogen-activated protein kinases (extracellular signal-regulated kinase, c-Jun N-terminal
126 cal analysis of the MAP2K1 downstream target extracellular signal-regulated kinase demonstrated its p
127 1P receptor 3 (S1pr3) through Rho kinase and extracellular signal-regulated kinase-dependent pathway.
128 m after acute cocaine administration, via an extracellular-signal regulated kinase-dependent de novo
129 ingly, knockdown of the canonical downstream extracellular signal-regulated kinase did not reproduce
130 ed protein kinase C (PKC) in the cytosol and extracellular signal regulated kinase (ERK) in the cytos
132 alized at 24 h, while the phosphorylation of extracellular signal regulated kinase (ERK) was increase
133 actor (FGF) proteins that signal through the extracellular signal regulated kinase (ERK)/mitogen acti
136 y slightly reduced downstream phosphorylated extracellular signal-regulated kinase (ERK) (pERK) level
137 acid dibutylester and imiquimod showed that extracellular signal-regulated kinase (ERK) 1/2 cascade
139 APK target gene expression and assessment of extracellular signal-regulated kinase (ERK) 1/2 phosphor
140 y upregulated, but uncoupled from downstream extracellular signal-regulated kinase (ERK) 1/2 signalin
141 R1 by RO5166017 increased phosphorylation of extracellular signal-regulated kinase (ERK) 1/2, and pro
142 hrough the posttranscriptional activation of extracellular signal-regulated kinase (ERK) 5 signaling,
143 ly localized D2R long isoform (D2LR) elicits extracellular signal-regulated kinase (ERK) activation a
144 d the dynamics of protein kinase C (PKC) and extracellular signal-regulated kinase (ERK) activation d
145 ositide 3-kinase (PI3Kgamma) plays a role in extracellular signal-regulated kinase (ERK) activation f
146 ies have suggested that dysregulation in RAS-extracellular signal-regulated kinase (ERK) activation i
147 ctivation of S6K1 during extinction required extracellular signal-regulated kinase (ERK) activation i
149 duced two mechanistically distinct phases of extracellular signal-regulated kinase (ERK) activation,
150 ained intracellular calcium mobilisation and extracellular signal-regulated kinase (Erk) activation,
151 p4k4 silencing in ECs enhanced basal Ras and extracellular signal-regulated kinase (Erk) activities,
153 l cell clusters display waves of oscillatory extracellular signal-regulated kinase (ERK) activity, wh
154 iated with a sustained increase in cytosolic extracellular signal-regulated kinase (ERK) activity.
155 ) and E-prostanoid receptor (EP) 3, enhanced extracellular signal-regulated kinase (Erk) and c-fos ph
156 o mitogen-activated protein kinases (MAPKs), extracellular signal-regulated kinase (ERK) and c-Jun N-
157 3T cell line and assessing activation of the extracellular signal-regulated kinase (ERK) and JUN N-te
158 e potent in inhibition of phosphorylation of extracellular signal-regulated kinase (ERK) and of cell
159 well as downstream pathways including STAT5, extracellular signal-regulated kinase (Erk) and p38.
161 xin-1 deficient B cells to the activation of extracellular signal-regulated kinase (ERK) and signal t
162 rosarcoma cells naturally expressing mutated extracellular signal-regulated kinase (ERK) antigen, the
165 lu5-scaffolding protein Homer2 and activated extracellular signal-regulated kinase (ERK) in an adapti
166 es cell proliferation and phosphorylation of extracellular signal-regulated kinase (ERK) in NF1 (-/-)
167 es cell proliferation and phosphorylation of extracellular signal-regulated kinase (ERK) in NF1(-/-)
168 by combined treatment with rapamycin and an extracellular signal-regulated kinase (ERK) inhibitor.
170 D8931, identified multiple components of the extracellular signal-regulated kinase (ERK) mitogen-acti
173 s report a fascinating phenotype whereby the extracellular signal-regulated kinase (ERK) pathway regu
174 and potently inhibited the pro-proliferative extracellular signal-regulated kinase (ERK) pathway; to
175 lic, vascular endothelial growth factor, and extracellular signal-regulated kinase (ERK) pathways are
176 omal signaling by protein kinase C (PKC) and extracellular signal-regulated kinase (ERK) pathways med
177 and migration of human keratinocytes through extracellular signal-regulated kinase (ERK) phosphorylat
178 f the mitogen-activated protein (MAP) kinase extracellular signal-regulated kinase (ERK) prevents ste
179 sponsive and oncogenically activated protein extracellular signal-regulated kinase (ERK) promotes mot
181 ellular signal-regulated kinase kinase (MEK)/extracellular signal-regulated kinase (ERK) scaffold, ki
182 ow that miR-431 overexpression activates Ras/extracellular signal-regulated kinase (Erk) signaling an
183 d by Jun N-terminal protein kinase (JNK) and extracellular signal-regulated kinase (ERK) signaling at
185 ventral tegmental area via modulation of the extracellular signal-regulated kinase (ERK) signaling pa
186 and mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) signaling pa
187 tations in the genes involved in the RAF/MEK/extracellular signal-regulated kinase (ERK) signaling pa
188 protein 2 (SREBP2) through activation of the extracellular signal-regulated kinase (ERK) signaling pa
189 es via the c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signaling pa
190 uclear factor (NF) kappaB signaling, whereas extracellular signal-regulated kinase (ERK) signaling wa
191 uced endocytosis is associated with impaired extracellular signal-regulated kinase (ERK) signaling, d
193 activation by GPCRs and CAMs, giving rise to extracellular signal-regulated kinase (ERK) signaling.
194 ge interactions in driving cAMP, calcium, or extracellular signal-regulated kinase (ERK) signaling.
196 disruption of the transcriptional control of extracellular signal-regulated kinase (ERK) signalling.
197 Here, we adapt the first-generation KTR for extracellular signal-regulated kinase (ERK) to allow eas
198 of NF-kappaB, c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase (ERK), and Akt (oc
199 bated with inhibitors of MEK (trametinib) or extracellular signal-regulated kinase (ERK), and some ce
200 ased mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK), mTOR, and p
201 ulin signaling/glucose homeostasis (ie, Akt, extracellular signal-regulated kinase (ERK), P70S6K), as
202 n of mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK), PI3K/AKT, a
203 gnalling pathways such as those regulated by extracellular signal-regulated kinase (ERK), protein kin
204 ing leukocyte protein of 76 kDa (SLP76), and extracellular signal-regulated kinase (Erk), were enhanc
205 e required for host immune response, whereas extracellular signal-regulated kinase (ERK), which is es
206 we investigated the DA D1 receptor (D1R) and extracellular signal-regulated kinase (ERK)-cAMP-respons
207 amide, KGF-pretreated mice also had apparent extracellular signal-regulated kinase (ERK)-driven proli
208 AF binding potential, and therefore altering extracellular signal-regulated kinase (ERK)-mediated PKM
209 ndritic cells (DCs) is triggered by IL-6 and extracellular signal-regulated kinase (ERK)-mitogen-acti
210 ciated herpesvirus (KSHV) requires sustained extracellular signal-regulated kinase (ERK)-p90 ribosoma
212 (psMEK) short-circuits the highly conserved Extracellular Signal-Regulated Kinase (ERK)-signaling ca
219 , p21-activated protein kinases (PAK1/2) and extracellular signal-regulated kinase (ERK)/C-Jun N-term
220 n development and to differentially regulate extracellular signal-regulated kinase (ERK)/mitogen-acti
221 of epidermal growth factor receptor (EGFR), extracellular signal-regulated kinase (ERK)1/2 or a TFF2
222 ses, mitogen-activated protein kinase [i.e., extracellular signal-regulated kinase (ERK)], and p70S6
223 y inhibitors of the prolyl isomerase Pin1 or extracellular signal-regulated kinases (ERK) 1/2 or by p
226 induce specific responses through a common, extracellular-signal regulated kinase (ERK)-dependent ca
227 r of mitogen-activated protein kinase (MAPK)/extracellular-signal-regulated kinase (ERK) (MEK) 1/2, w
228 se protein, which binds and dephosphorylates extracellular-signal-regulated kinase (ERK), leading to
230 the mitogen-activated protein (MAP) kinase (extracellular signal-regulated kinase [ERK]) signaling c
231 ind that the proteinase ADAM17 activates the extracellular signal-regulated kinases (ERK1/2) pathway
234 ession by activating a pathway that involves extracellular-signal-regulated kinase, IL-6 and the tran
235 cells was associated with phosphorylation of extracellular signal-regulated kinases, implying externa
236 causally linked with excessive activation of extracellular signal-regulated kinases in striatal neuro
237 ted by MEK (mitogen-activated protein kinase/extracellular signal-regulated kinase) inhibition or c-J
239 nib and the mitogen-activated protein kinase/extracellular signal-regulated kinase inhibitor selumeti
240 ed BRAF and mitogen-activated protein kinase/extracellular signal-regulated kinase inhibitor treatmen
242 s and Pam3Cys led to phosphorylation of ERK (extracellular signal-regulated kinase), JNK, and p38 mit
243 as EGFR or mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK)/ERK i
244 that the Ras/Raf/mitogen-activated protein, extracellular signal-regulated kinase kinase (MEK)/extra
245 anomas frequently develop resistance to MAPK/extracellular signal-regulated kinase kinase inhibitors
246 y niches counteracts combined BRAF/MEK (MAPK/extracellular signal-regulated kinase kinase) inhibitor
247 6 on both MEK-ERK (mitogen-activated protein/extracellular signal-regulated kinase kinase-extracellul
249 kout, while mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) and non
250 vation of a mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) negativ
251 ppaB kinase (IKK), mitogen-activated protein extracellular signal-regulated kinase (MEK), and Jun N-t
252 MP1 protein levels through activation of the extracellular signal-regulated kinase mitogen-activated
253 and a synthetic lethal interaction with the extracellular signal-regulated kinase mitogen-activated
255 ncrease in phosphorylation and activation of extracellular signal-regulated kinase/mitogen-activated
256 inal kinase (JNK) and c-Jun signals, but not extracellular signal-regulated kinase or Akt pathway act
257 -containing phosphatase [p-SHP2] and phospho-extracellular signal-regulated kinase [p-ERK]) is associ
258 ACD-induced cytoskeletal collapse activated extracellular signal-regulated kinase, p38, and c-Jun am
259 levels for the phosphorylated forms of AKT, extracellular signal-regulated kinase, p38, STAT1, and S
260 ls a new functional role for cocaine-induced extracellular signal-regulated kinase pathway independen
261 to enhance the efficacy of BRAF-MAPK kinase-extracellular signal-regulated kinase pathway inhibition
263 ), such as high expression of phosphorylated extracellular signal-regulated kinase (pERK) and reduced
264 the neuronal activity marker phosphorylated extracellular signal-regulated kinase (pERK) identified
266 of K-Ras effectors, including phosphorylated extracellular signal-regulated kinase, phosphorylated pr
267 cillatory magnitudes via modulation of local extracellular signal-regulated kinase phosphorylation (p
268 stress (S-SDS) induces D1 receptor-mediated extracellular signal-regulated kinase phosphorylation an
270 ression in primary OA chondrocytes inhibited extracellular signal-regulated kinase phosphorylation in
271 vemurafenib (480 mg/d) completely abrogated extracellular signal-regulated kinase phosphorylation of
272 the amygdala [CeA]) PACAP immunoreactivity, extracellular signal-regulated kinase phosphorylation, a
273 FSTL1 blocks Wnt7a-mediated repression of extracellular signal-regulated kinase phosphorylation, e
274 s phospho-Ser10-histone H3 without modifying extracellular-signal regulated kinase phosphorylation in
275 /calmodulin-dependent protein kinase II, and extracellular signal-regulated kinase, play key roles in
276 reased phosphorylation level of both Src and extracellular signal regulated kinase proteins and with
277 ibrosarcoma/mitogen-activated protein kinase/extracellular signal-regulated kinase (Raf/MEK/ERK) path
279 hibition of mitogen-activated protein kinase/extracellular signal-regulated kinase signaling 6 hours
280 a role of this holoenzyme in suppression of extracellular signal-regulated kinase signaling and prot
281 ndocytosis to block endosomal PACAP receptor extracellular signal-regulated kinase signaling attenuat
283 nd enhance or diminish AKT Ser/Thr kinase or extracellular signal-regulated kinase signaling in a bia
284 se/AKT, and mitogen-activated protein kinase/extracellular signal-regulated kinase signaling in mutat
286 e of knockout mice, suggesting that impaired extracellular signal-regulated kinase signaling mediated
288 g family, pyrin domain-containing-3, and p38/extracellular signal-regulated kinase signaling pathways
292 inositol-3'-kinase/protein kinase B and KRAS/extracellular-signal-regulated kinase signaling pathways
293 B cells from tolerant recipients had reduced extracellular signal-regulated kinase signalling after B
294 eton by dephosphorylating eplin at two known extracellular signal-regulated kinase sites, serine 362
295 epithelial cells; elevates protein kinase A, extracellular signal-regulated kinases, SMAD and signal
296 atidylinositol 3-kinase-Akt, Ras-Raf-1, MEK1/extracellular signal-regulated kinase, sphingolipid, and
297 , A61603 activation of cardioprotective ERK (extracellular signal-regulated kinase) was markedly impa
298 Mechanistically, reactive oxygen species and extracellular signal-regulated kinase were found to medi
299 tivates the mitogen-activated protein kinase extracellular-signal-regulated kinase, which then direct
300 ular, disruption of mGlu5 phosphorylation by extracellular signal-regulated kinase within this brain