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1 phorylation and activation of KSR-bound MEK (mitogen-activated protein kinase kinase).
2 locked by inhibitors of protein kinase C and mitogen-activated protein kinase kinase.
3 inhibitors of either farnesyl transferase or mitogen-activated protein kinase kinase.
4 n is a metalloprotease that cleaves upstream mitogen-activated protein kinase kinases.
5 ted and ddPCR confirmed somatic mutations in mitogen activated protein kinase kinase 1 (MAP2K1), the
6 lleles in Ras-like without CAAX 1 (RIT1) and mitogen-activated protein kinase kinase 1 (MAP2K1) and p
7 n has been linked to its ability to activate mitogen-activated protein kinase kinase 1 (MEK) and mito
9 Overexpression of V1, V2, or GIT1 activated mitogen-activated protein kinase kinase 1 (MEK1) and ext
10 gulated kinase (ERK)1/2 and Akt and both the mitogen-activated protein kinase kinase 1 (MEK1) and pho
12 AK-null cells, constitutively activated (CA) mitogen-activated protein kinase kinase 1 (MEK1) restore
13 s article, we demonstrate that LPA activates mitogen-activated protein kinase kinase 1 (MEKK1) in a G
14 Ectopic expression of constitutively active mitogen-activated protein kinase kinase 1 (MKK1) resulte
15 rrolo[3,4-c]carbazole-12-p ropanenitrile and mitogen-activated protein kinase kinase 1 2-(2-amino-3-m
16 ion of BRCA1-induced ERK1/2 activation using mitogen-activated protein kinase kinase 1 and 2 (MEK1/2)
17 The expression of constitutively activated mitogen-activated protein kinase kinase 1 enhanced caspa
19 y, and the effects of LT were independent of mitogen-activated protein kinase kinase 1 inhibition.
20 ression of the alpha7 integrin or use of the mitogen-activated protein kinase kinase 1 inhibitor U012
21 FR with AG1478 or small interfering RNA), or mitogen-activated protein kinase kinase 1 or 2 (MKK1/2 w
22 activating mutation in exon 2 of MEK1 (i.e., mitogen-activated protein kinase kinase 1 or MAP2K1) tha
24 othecin by expression of constitutive active mitogen-activated protein kinase kinase 1, an upstream k
25 that the hepatocyte growth factor activator, mitogen-activated protein kinase kinase 1, and phosphati
26 sed by pharmacologic and siRNA inhibitors of mitogen-activated protein kinase kinase 1/2 (MEK1/2) and
27 phynylthio)butadiene]-specific inhibitors of mitogen-activated protein kinase kinase 1/2 (MEK1/2) blo
28 ERK1/2), and the combination of SMI-4a and a mitogen-activated protein kinase kinase 1/2 (MEK1/2) inh
29 gonism of PGE2 release was achieved with the mitogen-activated protein kinase kinase 1/2 (MEK1/2) inh
30 between 7-hydroxystaurosporine (UCN-01) and mitogen-activated protein kinase kinase 1/2 (MEK1/2) inh
31 tion that 20S reduction has little effect on mitogen-activated protein kinase kinase 1/2 (MEK1/2) sig
32 , cardiac expression of phospho-Akt, phospho-mitogen-activated protein kinase kinase 1/2 and phospho-
34 anner, combined exposure to OSU-03012 with a mitogen-activated protein kinase kinase 1/2 inhibitor, p
36 ess signaling pathways demonstrated that the mitogen-activated protein kinase kinase 1/2 pathway acti
37 by cytokines and suppressed by inhibition of mitogen-activated protein kinase kinase 1/2, whereas STE
40 al-regulated kinases 1/2 phosphorylation was mitogen-activated protein kinase kinases 1/2 dependent b
42 nhibitor of the dual-specificity kinases MEK(mitogen-activated protein kinase kinase) -1 and MEK2 , i
44 Here, we demonstrate that acetylation of the mitogen-activated protein kinase kinase-1 (MEK1) stimula
47 idated six candidate proteins, including the mitogen-activated protein kinase kinase 2 (MEK2), that i
49 activation could be blocked by RNAi against mitogen-activated protein kinase kinase 3 and 6 (MKK3/6)
50 Even though 34F(2) has LeTx, there was no mitogen-activated protein kinase kinase 3 cleavage and p
51 orylation of p38 and its upstream regulators mitogen-activated protein kinase kinase 3/6 and apoptosi
52 stressed by osmotic shock (OSM) activate the mitogen-activated protein kinase kinase(3/6)-p38 signali
53 (MAP) kinase cascade consisting of GhMAP3K15-Mitogen-activated Protein Kinase Kinase 4 (GhMKK4)-Mitog
54 un NH(2)-terminal kinase activating kinase 1/mitogen-activated protein kinase kinase 4 (JNKK1/MKK4) a
55 ses HAESA (HAE) and HAESA-like 2 (HSL2), the Mitogen-Activated Protein Kinase Kinase 4 (MKK4) and MKK
56 ine-inducible, constitutively active, mutant mitogen-activated protein kinase kinase 4 (MKK4) into th
58 l death in vitro and in vivo by inactivating mitogen-activated protein kinase kinase 4 (MKK4), JNK, a
60 ic expression of JNK and its upstream kinase mitogen-activated protein kinase kinase 4 led to DNA dam
61 R256C mutation revealed attenuation of MKK4 (mitogen-activated protein kinase kinase 4) activation th
62 kinase/extracellular signal-related kinase 1/mitogen-activated protein kinase kinase 4), c-Jun N-term
63 MAP2K4 encodes a dual-specificity kinase (mitogen-activated protein kinase kinase 4, or MKK4) that
64 rough development in floral receptacles in a MITOGEN-ACTIVATED PROTEIN KINASE KINASE 4/5-dependent ma
65 m signaling showed a prominent activation of mitogen-activated protein kinase kinase 4/6 and c-Jun NH
66 /2, p38 stress-activated protein kinase, and mitogen-activated protein kinase kinases 4/7 shows littl
71 cific transgenic overexpression of activated mitogen-activated protein kinase kinase 6, a direct indu
72 mice with fibroblast-specific activation of mitogen-activated protein kinase kinase 6-p38 developed
73 proapoptotic protein JNK1 by upregulation of mitogen-activated protein kinase kinase 7 (MKK7) and dow
74 as associated with increases in the upstream mitogen-activated protein kinase kinase 7 (MKK7) and the
76 ivates downstream effectors that include the mitogen-activated protein kinase kinase 7 (MKK7)/c-Jun-N
77 lightly stimulated the JNK-activating kinase mitogen-activated protein kinase kinase 7, the latter wa
81 chain phosphorylation by PAK is mediated by mitogen-activated protein kinase kinase and extracellula
82 n was partially blocked by inhibition of the mitogen-activated protein kinase kinase and protein kina
84 in kinase B and a pathway involving DSOR1, a mitogen-activated protein kinase kinase, and an extracel
85 hatidyl inositol 3-kinase, protein kinase C, mitogen-activated protein kinase kinase, and p38-mitogen
86 ypoxic A431 cells, whereas inhibition of the mitogen-activated protein kinase kinase by PD98059 reduc
88 translocation to the cytosol (as assessed by mitogen-activated protein kinase kinase cleavage), K(+)
90 n kinase kinase kinase, or in MKK4/MAP2K4, a mitogen-activated protein kinase kinase directly downstr
91 K4/MAP2K4, mice lacking MKK7/MAP2K7, another mitogen-activated protein kinase kinase directly downstr
92 through Akt/protein kinase B (Akt/PKB), the mitogen-activated protein kinase kinase DSOR1, and extra
94 because blocking this pathway, but not MEK (mitogen-activated protein kinase kinase)/ERK (extracellu
95 (phosphatidylinositol 3-kinase)/Akt and MEK (mitogen-activated protein kinase kinase)/Erk pathways pr
96 e blocked both by pertussis toxin and by the mitogen-activated protein kinase kinase/ERK inhibitor [1
97 h the PPARgamma receptor but may involve the mitogen-activated protein kinase kinase/ERK pathway and
98 tion of the epidermal growth factor receptor-mitogen-activated protein kinase kinase-extracellular si
102 expression in a manner dependent on Mek/Erk (mitogen-activated protein kinase kinase/extracellular si
103 s induced by concomitant interruption of the mitogen-activated protein kinase kinase/extracellular si
104 mulated translation and signaled through the mitogen-activated protein kinase kinase/extracellular si
105 duction involving protein kinase A, src, and mitogen-activated protein kinase kinase/extracellular si
106 rst examples of T3SS effectors implicated in mitogen-activated protein kinase kinase/extracellular si
107 ation of transforming growth factor beta and Mitogen-activated protein kinase kinase/extracellular si
108 ating event [i.e., the activation of the Raf/mitogen-activated protein kinase kinase/extracellular si
109 /calmodulin-dependent kinase II) or MEK/ERK (mitogen-activated protein kinase kinase/extracellular si
110 n target of rapamycin (mTOR) pathway and the mitogen-activated protein kinase kinase/extracellular si
111 de content of human adipocytes by activating mitogen-activated protein kinase kinase/extracellular si
112 p-regulation of IL-8 in DU145 depends on the mitogen-activated protein kinase kinase/extracellular si
113 caused a robust and sustained activation of mitogen-activated protein kinase kinase/extracellular si
114 15-mediated growth advantage is abolished by mitogen-activated protein kinase kinase/extracellular si
116 effect was decreased by a M3R antagonist, a mitogen-activated protein kinase kinase/extracellular si
117 n of p53 at Ser-15 and the initiation of the mitogen-activated protein kinase kinase/extracellular-re
119 as an intracellular endopeptidase targeting mitogen-activated protein kinase kinases, growing eviden
120 d-type ARAF, this mutant was a highly active mitogen-activated protein kinase kinase in vitro and was
121 ein kinase kinase, indicating that potential mitogen-activated protein kinase kinase-independent Raf
122 rmacological inhibition of the Raf substrate mitogen-activated protein kinase kinase, indicating that
123 lockade of this rebound activation with MEK (mitogen-activated protein kinase kinase) inhibition enha
124 ensis-infected mice with the highly-specific mitogen activated protein kinase kinase inhibitor, CI-10
128 ration were inhibited after treatment with a mitogen-activated protein kinase kinase inhibitor, U0126
130 re given intrathalamic infusions of the MEK (mitogen-activated protein kinase-kinase) inhibitor 1,4-d
131 inhibited, respectively, by U0126, PD98059 (mitogen-activated protein kinase kinase inhibitors), SP6
132 -dependent protein kinase signaling, and two mitogen-activated protein kinase kinase inhibitors, U012
133 e cholangiocytes that was blocked by PKA and mitogen-activated protein kinase kinase inhibitors.
134 ASK1, also known as MAP3K5), a member of the mitogen-activated protein kinase kinase kinase (MAP3K) f
136 Mixed-lineage kinase-3 (MLK3) is a mammalian mitogen-activated protein kinase kinase kinase (MAP3K) t
140 nd repressing the downstream gene encoding a mitogen-activated protein kinase kinase kinase (MAPKKK)
142 tosis signal-regulating kinase 1 (ASK1) is a Mitogen-Activated Protein Kinase Kinase Kinase (MAPKKK,
143 IS8 gene revealed that it encodes a putative mitogen-activated protein kinase kinase kinase (MAPKKK;
144 effect of expressing a heterologous tobacco mitogen-activated protein kinase kinase kinase (Nicotian
147 by current methods, we discovered recurrent mitogen-activated protein kinase kinase kinase 1 (Map3k1
148 action is not fully understood, a functional mitogen-activated protein kinase kinase kinase 1 (MAP3K1
150 ylation of c-Jun caused by overexpression of mitogen-activated protein kinase kinase kinase 1 (Mekk1)
151 ondrial ribosomal protein S30 gene (MRPS30), mitogen-activated protein kinase kinase kinase 1 gene (M
152 appaB pathway, including the upstream kinase mitogen-activated protein kinase kinase kinase 14 (MAP3K
154 usly known and unknown to be associated with mitogen-activated protein kinase kinase kinase 2 (MEKK2)
155 401.3, c.1323C>G; NP_002392, p.Iso441Met) in mitogen-activated protein kinase kinase kinase 3 (MAP3K3
156 ich protein kinase C substrate (MARCKS), and mitogen-activated protein kinase kinase kinase 3 (MAP3K3
157 lar kinase expression library, we identified mitogen-activated protein kinase kinase kinase 8 (MAP3K8
159 er Osaka thyroid (COT) kinase, also known as mitogen-activated protein kinase kinase kinase 8 (MAP3K8
160 to stimulate cell proliferation involves the mitogen-activated protein kinase kinase kinase B-Raf, we
162 nesis by down-regulating the ortholog of the mitogen-activated protein kinase kinase kinase dual leuc
163 ancer osaka thyroid (COT) is a member of the mitogen-activated protein kinase kinase kinase family of
164 that Wallenda (Wnd), a protein kinase of the mitogen-activated protein kinase kinase kinase family, b
165 a activated kinase-1 (TAK1), a member of the mitogen-activated protein kinase kinase kinase family, h
166 eta-activated kinase (TAK1), a member of the mitogen-activated protein kinase kinase kinase family.
167 mixed lineage kinases (MLKs), members of the mitogen-activated protein kinase kinase kinase family.
169 n activation by inhibiting the expression of mitogen-activated protein kinase kinase kinase kinase 1
170 RPs for inflammation genes revealed that the mitogen-activated protein kinase kinase kinase kinase 4
171 e suggested a role for endothelial cell (EC) mitogen-activated protein kinase kinase kinase kinase 4
172 Previous studies revealed a paradox whereby mitogen-activated protein kinase kinase kinase kinase 4
173 Here we demonstrate that the Sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4
174 By quantitative proteomics, we identified mitogen-activated protein kinase kinase kinase kinase 4
176 nine nucleotide exchange factor Asef and the mitogen-activated protein kinase kinase kinase kinase ge
177 , our studies focused on the redox-sensitive mitogen-activated protein kinase kinase kinase known as
178 g a point mutation that renders inactive the mitogen-activated protein kinase kinase kinase MEKK4 exh
180 (Arabidopsis thaliana) gene MEKK1 encodes a mitogen-activated protein kinase kinase kinase that has
181 hase of APAP-induced JNK activation, but the mitogen-activated protein kinase kinase kinase that medi
182 ibers, including, most prominently, MEKK4, a mitogen-activated protein kinase kinase kinase that was
183 Mixed lineage kinase 3 (MLK3) functions as a mitogen-activated protein kinase kinase kinase to activa
185 eviously, we reported that both MAPKKKalpha (mitogen-activated protein kinase kinase kinase) and the
186 (2+) or cAMP on regrowth require the MAPKKK (mitogen-activated protein kinase kinase kinase) DLK-1.
188 tion was dependent on activation of RhoA and mitogen-activated protein kinase kinase kinase, MEKK1, l
189 also known as dual leucine zipper kinase), a mitogen-activated protein kinase kinase kinase, or in MK
190 optosis signal-regulating kinase 1 (ASK1), a mitogen-activated protein kinase kinase kinase, plays a
191 stimulates the association of Dab2 with the mitogen-activated protein kinase kinase kinase, TAK1.
192 Recent studies have shown that mutations in mitogen-activated protein kinase kinase kinase-4 (Mekk4)
196 finger homeodomain transcription factors and mitogen-activated protein kinase kinase kinases, respect
198 stic phenotype that was sensitive to RAF and mitogen-activated protein kinase kinase (MAP2K1) inhibit
200 's pro-survival effects were associated with mitogen activated protein kinase kinase (MAPKK)-->p42/p4
201 , proteolytically inactivates members of the mitogen-activated protein kinase kinase (MAPKK or MEK) f
202 se known targets include five members of the mitogen-activated protein kinase kinase (MAPKK) family o
203 een demonstrated to cleave and to inactivate mitogen-activated protein kinase kinases (MAPKKs) that p
204 st Saccharomyces cerevisae has four distinct mitogen-activated protein kinase kinases (MAPKKs), each
205 first trimester decidua via a Gq-Ca(2+)-cSrc-mitogen-activated protein kinase kinase-mediated pathway
207 nositol 3-kinase (PI 3-kinase) (wortmannin), mitogen-activated protein kinase kinase (MEK) (PD98059),
208 e protein kinase Calpha/betaI isozyme (PKC), mitogen-activated protein kinase kinase (MEK) 1 and 2, a
209 Enforced expression of constitutively active mitogen-activated protein kinase kinase (MEK) 1 or myris
210 microg/mL) inhibited the kinase activity of mitogen-activated protein kinase kinase (MEK) 1/2 and re
212 , we show that pharmacological inhibition of mitogen-activated protein kinase kinase (MEK) activates
213 t inhibition of PKD blocks mitotic Raf-1 and mitogen-activated protein kinase kinase (MEK) activation
214 racellular glutathione levels, which inhibit mitogen-activated protein kinase kinase (MEK) activity t
216 The kinase pathway comprising RAS, RAF, mitogen-activated protein kinase kinase (MEK) and extrac
217 of phosphatidylinositol 3-kinase (PI3K) and mitogen-activated protein kinase kinase (MEK) but are kn
218 KSR1 mutant bound constitutively to RAF and mitogen-activated protein kinase kinase (MEK) but could
219 utadiene (U0126) of an HGF downstream kinase mitogen-activated protein kinase kinase (MEK) induced th
221 h paradoxical MAPK activation; addition of a mitogen-activated protein kinase kinase (MEK) inhibitor
222 lated kinase (ERK) pathway as treatment with mitogen-activated protein kinase kinase (MEK) inhibitor
225 anced cutaneous melanoma were treated with a mitogen-activated protein kinase kinase (MEK) inhibitor
226 fibroblast growth factor receptor (FGFR) or mitogen-activated protein kinase kinase (MEK) inhibitor
227 of rapamycin (mTOR) inhibitors, but not the mitogen-activated protein kinase kinase (MEK) inhibitor,
228 typically considered an exquisitely specific mitogen-activated protein kinase kinase (MEK) inhibitor,
229 e received intraperitoneal injections of the Mitogen-activated protein kinase kinase (MEK) inhibitor,
230 spatial learning, which can be reversed by a mitogen-activated protein kinase kinase (MEK) inhibitor.
231 tant BRAF(V600E) tumours but, in contrast to mitogen-activated protein kinase kinase (MEK) inhibitors
232 rous retinal disturbances in patients taking mitogen-activated protein kinase kinase (MEK) inhibitors
233 ary Nras(G12D) AMLs with 2 potent allosteric mitogen-activated protein kinase kinase (MEK) inhibitors
234 o novel series of highly potent biaryl amine mitogen-activated protein kinase kinase (MEK) inhibitors
236 is known to be mediated by the canonical Raf-mitogen-activated protein kinase kinase (MEK) kinase cas
238 ing the cells with an inhibitor (PD98059) of mitogen-activated protein kinase kinase (MEK) or by tran
239 showing that inhibitors of BRAF-V600E and/or mitogen-activated protein kinase kinase (MEK) reach thei
242 any additional treatment, the inhibition of mitogen-activated protein kinase kinase (MEK) with U0126
243 inositide-3 kinase (PI3 kinase), Akt, Raf-1, mitogen-activated protein kinase kinase (MEK), and extra
244 ctivity and basal and stimulated Ras, Raf-1, mitogen-activated protein kinase kinase (MEK), and MAPK
245 geting the shared ERK1/2 upstream activator, mitogen-activated protein kinase kinase (MEK), and trans
247 eptors produced either enhanced or sustained mitogen-activated protein kinase kinase (MEK), Casitas B
248 nges in calcium, and phosphorylation of Akt, mitogen-activated protein kinase kinase (MEK), extracell
249 Ras-mediated signaling pathway involving the mitogen-activated protein kinase kinase (MEK), known to
250 paB, extracellular signal-regulated kinase > mitogen-activated protein kinase kinase (MEK), p38, and
251 I HDACs requires activity of the ERK kinase, mitogen-activated protein kinase kinase (MEK), revealing
252 small-molecule screen found an inhibitor of mitogen-activated protein kinase kinase (MEK), which act
254 pathways known to couple to translation, the mitogen-activated protein kinase kinase (MEK)-extracellu
255 therapeutic importance of the activated BRAF-mitogen-activated protein kinase kinase (MEK)-extracellu
261 a poor prognosis, but targeting the RAS/RAF/mitogen-activated protein kinase kinase (MEK)/extracellu
263 overexpressing RARalpha2 activated STAT3 and mitogen-activated protein kinase kinase (MEK)/extracellu
265 intrinsic chemoresistance by activating the mitogen-activated protein kinase kinase (MEK)/extracellu
266 emurafenib, which selectively inhibits B-RAF/mitogen-activated protein kinase kinase (MEK)/extracellu
267 k2(fl/fl-Cre)) and mice expressing activated mitogen-activated protein kinase kinase (Mek)1 in the he
268 usly, we showed that Cdk5 phosphorylation of mitogen-activated protein kinase kinase (MEK)1 inhibits
270 f mitogen-activated protein kinase activator mitogen-activated protein kinase kinase (MEK)1, and the
271 th factor receptor (ERBB1) via a Galpha(i)-, mitogen-activated protein kinase kinase (MEK)1/2-, and m
272 tivation of the PI3Kshort right arrowAKT and mitogen-activated protein kinase kinase (MEK)short right
273 rine neutrophils, leading to the cleavage of mitogen-activated protein kinase kinase/MEK/MAPKK 1-4 an
274 hosphorylation of B-cell linker protein, the mitogen-activated protein kinase kinase MEK1/2, and ERK,
275 98059 and UO126, selective inhibitors of the mitogen-activated protein kinase kinase MEK1/2, in a dos
276 Here we show that PI3K-C2beta regulates mitogen-activated protein kinase kinase (MEK1/2) and ext
277 niquely used for differential binding of two mitogen-activated protein kinase kinases, MEK5 and MKK7,
280 growth factor-beta-activated kinase 1 (TAK1)-mitogen-activated protein kinase kinase (MKK) 3/6-p38alp
281 ludes proteasome inactivation, activation of mitogen-activated protein kinase kinase (MKK)3/MKK6, act
284 new integrin ligation and requires both the mitogen-activated protein kinase kinase MKK4 and p21-act
285 ghly specific protease, exclusively cleaving mitogen-activated protein kinase kinases (MKKs) and rode
287 atic loss of phosphorylation of MKK3 and -6, mitogen-activated protein kinase kinases (MKKs) regulate
288 some inhibitor lactacystin, by inhibitors of mitogen-activated protein kinase kinase or protein kinas
290 n M1 CM that induces CXCL12 expression via a mitogen-activated protein kinase kinase-p38-signal trans
292 data revealed that the expression of several mitogen-activated protein kinase kinase-regulatory genes
293 particular, we report synergistic effects of mitogen-activated protein kinase kinase, ribosomal S6 ki
295 Wnt signals, a temporal control pathway, and mitogen-activated protein kinase kinase signaling contro
296 f bone marrow-derived dendritic cells with a mitogen activated protein kinase kinase-specific inhibit
297 a synthetic peptide substrate and endogenous mitogen-activated protein kinase kinase substrates and k
298 itor 2'-amino-3'-methoxyflavone (PD98059) of mitogen-activated protein kinase kinase, the upstream ki
300 s encoding ENHANCED DISEASE SUSCEPTIBILITY1, mitogen-activated protein kinase kinase, WRKY, PATHOGENE
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