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1 osine and dual-specific phosphatases, sodium orthovanadate.
2 y ligands such as MgATP, MgADP, or inorganic orthovanadate.
3 ts in its apparent affinity for ATP, H+, and orthovanadate.
4 UV-C, gamma radiation, TNF-alpha, and sodium orthovanadate.
5 ), with optimal effects seen at 25 microg/ml orthovanadate.
6 aration containing vanadyl ribonucleoside or orthovanadate.
7 were reversed by pertussis toxin and sodium orthovanadate.
8 in surface AMPAR clusters was unaffected by orthovanadate.
9 eptor (AMPAR) subunits, an effect blocked by orthovanadate.
10 opiperazines and the ATPase inhibitor sodium orthovanadate.
11 more sensitive to beryllium fluoride than to orthovanadate.
12 state at NBD2 by the gamma-phosphate analog orthovanadate.
13 ited by TNF, and this was reversed by sodium orthovanadate.
14 presence of the phosphatase inhibitor sodium orthovanadate.
15 ase inhibitors phenylarsine oxide and sodium orthovanadate.
16 n cells pretreated with the PTPase inhibitor orthovanadate.
17 e in either apoptosis or survival induced by orthovanadate.
18 otein-tyrosine phosphatase inhibitor, sodium orthovanadate.
20 D98,059 (20 microM) or phosphatase inhibitor orthovanadate (30 microM) completely blocked the potenti
22 n of phosphatase inhibitors (5 mmol/l sodium orthovanadate, 50 mmol/l sodium fluoride, or 5 mmol/l ED
23 ysis with the tyrosine phosphatase inhibitor orthovanadate (500 microM) prevented the actions of both
24 r cells treated with interleukin-6 (IL-6) or orthovanadate (a general activator of STATs) were fracti
25 er preincubation of oocytes with 1 mM sodium orthovanadate (a protein tyrosine phosphatase inhibitor)
26 red insulin's effect on MAPK activity, while orthovanadate (a tyrosine phosphatase inhibitor), inhibi
29 hat the inhibitory form is usually monomeric orthovanadate, a particularly good inhibitor of phosphat
30 nt HCD57 murine cell line with 70 micromol/L orthovanadate, a tyrosine phosphatase inhibitor, resulte
31 The tyrosine phosphatase inhibitor sodium orthovanadate ablated the inhibitory effects of roscovit
33 ally, we show that the phosphatase inhibitor orthovanadate acts as does CHI to render cells susceptib
35 rthermore, the well studied PTPase inhibitor orthovanadate also induced protein tyrosine phosphorylat
36 (Sp)-cAMP, cells were pretreated with sodium orthovanadate, an inhibitor of phosphotyrosine phosphata
37 Culture of normal erythroid progenitors with orthovanadate, an inhibitor of protein tyrosine phosphat
39 tion, and two general PTP inhibitors, sodium orthovanadate and bpV(pic), dramatically rescued the cel
40 otein-tyrosine-phosphatase inhibitors sodium orthovanadate and dephostatin prevented PPARgamma ligand
42 that was abolished in the presence of sodium orthovanadate and inhibited significantly by the sulfhyd
43 ibited by the tyrosine phosphatase inhibitor orthovanadate and is particularly sensitive to inhibitio
45 otein tyrosine phosphatase (PTP) inhibitors, orthovanadate and phenylarsine oxide, selectively block
48 inhibitors of tyrosine phosphatases (sodium orthovanadate and sodium molybdate) but not by inhibitor
49 ith a tyrosine phosphatase inhibitor (sodium orthovanadate) and T-cell activation signals (phorbol 12
50 rotein kinase (MAPK) was poorly activated by orthovanadate, and inhibition of MAPK with PD98059 block
52 vely high Km for ATP (1.9 mM), inhibition by orthovanadate, and the ability to specifically bind an a
53 ptimal at pH 7; 2) potently inhibited by F-, orthovanadate, and Zn2+ > Co2+ > Mn2+ but unaffected by
57 Finally, in dissociated hippocampal neurons, orthovanadate blocked the ability of DHPG to reduce the
62 (B44) and a tyrosine phosphatase inhibitor (orthovanadate), changes in both CCK- and TPA-stimulated
63 te is due to formation of a pentacoordinated orthovanadate complex at the phosphorylation site, corre
66 -1 cells with either cycloheximide or sodium orthovanadate had little effect on the early peak of ERK
67 eral other ABC proteins and was inhibited by orthovanadate in a profile diagnostic of ABC transporter
69 cal for the survival of erythroid cells, and orthovanadate in the absence of EPO both maintained expr
70 ells with the tyrosine phosphatase inhibitor orthovanadate in the presence of insulin or okadaic acid
71 promotion of pro-MMP-2 activation by sodium orthovanadate in the presence of suboptimal concentratio
72 posure to the tyrosine phosphatase inhibitor orthovanadate increases tyrosine phosphorylation of beta
73 otein tyrosine phosphatase inhibitor, sodium orthovanadate, increases eNOS tyrosine phosphorylation.
76 plete inhibition of ATPase activity, whereas orthovanadate inhibited exclusively the PC-stimulated AT
78 rotein tyrosine phosphatase inhibitor sodium orthovanadate inhibits fertilization suggest that protei
79 dimer is most prominent upon the addition of orthovanadate (K(i) = 0.70 +/- 0.20 microM) and PhAH, in
82 ts or T-cells with the phosphatase inhibitor orthovanadate markedly abolished MIP1beta-induced chemot
84 rt that the addition of BeF(3)(-) and sodium orthovanadate (Na(3)VO(4)) to medium containing digitoni
86 n via the patch pipette of 200 microM sodium orthovanadate (Na3VO4), which inhibits tyrosine phosphat
88 SHP1 overrecruitment, treatment with sodium orthovanadate or a novel inhibitor with micromolar activ
89 sing either the phosphatase inhibitor sodium orthovanadate or antisense oligonucleotides prevents the
91 hibition of phosphoprotein phosphatases with orthovanadate or fluoride yielded a global protein phosp
92 otactic activity in HAEC treated with sodium orthovanadate or MKP-1 antisense oligonucleotides is due
94 presence of a phosphatase inhibitor, sodium orthovanadate, or antisense oligonucleotides, suggesting
95 tyrosine phosphatase (PTPase) inhibition by orthovanadate (OVA) showed that this Src activity is hig
98 of the tyrosine phosphatase inhibitor sodium orthovanadate prior to ethanol restored tyrosine phospho
99 splayed a 40-fold decrease in sensitivity to orthovanadate, reflecting a shift in equilibrium from th
101 ld type or mutant forms of PECAM-1 to sodium orthovanadate resulted in high levels of cytoplasmic tyr
102 mutant cells with the phosphatase inhibitor orthovanadate resulted in strong coordinate elevation of
104 ct, like S1P-mediated ERK1/2 inhibition, was orthovanadate-sensitive and pertussis toxin-insensitive.
105 via an ATP-driven, protonophore-insensitive, orthovanadate-sensitive mechanism, equating with export
106 These results suggest that a TPA-inducible, orthovanadate-sensitive protein-tyrosine phosphatase may
107 ase activity by phenylarsine oxide or sodium orthovanadate shifted ventricular hyperpolarization-acti
108 d the reversal and phosphatase inhibition by orthovanadate significantly accelerated the recovery.
110 ocytes also displayed GTP gamma S and sodium orthovanadate stimulation of actin comet tails on GLUT4
112 imulated KDR activity was impaired by sodium orthovanadate, suggesting that the inhibitory activity o
113 1/2 activity was abolished by treatment with orthovanadate, suggesting the involvement of a tyrosine
114 Inhibition of dephosphorylation with sodium orthovanadate suggests that this effect is at least part
115 Upon activation of signaling by IL-6 or orthovanadate the respective Tyr-phosphorylated STAT spe
116 one in the presence of 100 micromol/L sodium orthovanadate to prevent enzymatic redistribution of lip
117 sence and presence of the phosphate analogue orthovanadate, to determine the roles the nucleoside moi
119 PI-3 kinase activity, triggered apoptosis in orthovanadate-treated cells, suggesting a critical role
121 Orthophosphate and the oxoanion analogues orthovanadate, tungstate, molybdate, arsenate, and sulfa
122 ormation in the presence of Mg(2+), ADP, and orthovanadate (V(i)), a photoreactive phosphate analog w
123 of the stable myosin subfragment 1(S1).MgADP.orthovanadate (Vi) complex results in oxidation of an ac
125 his reason, we have carried out studies with orthovanadate (Vi), a phosphate analog which has the pot
126 can hydrolyze ATP simultaneously, we used an orthovanadate (Vi)-induced ADP-trapping technique (P-gp.
130 ructure of AcpA complexed with the inhibitor orthovanadate, which is the first structure of any F. tu
131 h Gly-371 were highly resistant to inorganic orthovanadate, with IC(50) values at least 10-fold above
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