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1 1beta, IL-6, inducible NO synthase, TNF, and reactive oxygen intermediate.
2 thogen strain causes the rapid production of reactive oxygen intermediates.
3 hesion to endothelium followed by release of reactive oxygen intermediates.
4 ivity for growth and enhanced sensitivity to reactive oxygen intermediates.
5  can react with oxygen to generate cytotoxic reactive oxygen intermediates.
6  to infection, which includes the release of reactive oxygen intermediates.
7 d inhibition in astrocytes is independent of reactive oxygen intermediates.
8 ous to our understanding of defenses against reactive oxygen intermediates.
9 ogression of renal disease via generation of reactive oxygen intermediates.
10 rom PPARgamma, to modulate the production of reactive oxygen intermediates.
11 and viability via a process(es) dependent on reactive oxygen intermediates.
12 e latter two compounds are known to generate reactive oxygen intermediates.
13 state acetate (PMA)-stimulated production of reactive oxygen intermediates.
14 ion and the subsequent massive production of reactive oxygen intermediates.
15 ic heavy metals and protection of cells from reactive oxygen intermediates.
16 n indirect effect of COX products, including reactive oxygen intermediates.
17 uivalents to protect cellular integrity from reactive oxygen intermediates.
18 to be activated by many compounds, including reactive oxygen intermediates.
19 gested organisms are likely to be exposed to reactive oxygen intermediates.
20 tor alpha-induced mitochondrial cell-derived reactive oxygen intermediates.
21 nst various inducers of apoptosis, including reactive oxygen intermediates.
22 known to be activated by a process involving reactive oxygen intermediates.
23 ys 890, abolishing its ability to synthesize reactive oxygen intermediates.
24  agonist salicylic acid and the synthesis of reactive oxygen intermediates.
25 ss signals, such as DNA damage, hypoxia, and reactive oxygen intermediates.
26 tion via redox cycling and the generation of reactive oxygen intermediates.
27 dent phagocytosis and subsequent exposure to reactive oxygen intermediates.
28 DPH oxidase and the concomitant reduction in reactive oxygen intermediates.
29  of reactive nitrogen intermediates, but not reactive oxygen intermediates.
30  mediated in part by increased resistance to reactive oxygen intermediates.
31 ric oxide congener formed in the presence of reactive oxygen intermediates.
32 ular iron to the parasite, and production of reactive oxygen intermediates.
33            N-acetyl cysteine (a scavenger of reactive oxygen intermediates) abolished the ability of
34                                      Imaging reactive oxygen intermediate activities in phagosomes re
35 , myeloid cells, and a combination of NO and reactive oxygen intermediates all contribute to a common
36 s synthesized at high levels by cells during reactive oxygen intermediate and nitrogen intermediate p
37 quinone), a redox cycling reagent, generates reactive oxygen intermediates and causes oxidative injur
38 nd ADCC activity, while DC failed to release reactive oxygen intermediates and demonstrated minimal A
39 ypersensitive cell death in soybean cells by reactive oxygen intermediates and functions independentl
40  as an antioxidant by directly reacting with reactive oxygen intermediates and has a vital role in de
41 istinct roles in P. aeruginosa resistance to reactive oxygen intermediates and heat.
42                                         Both reactive oxygen intermediates and iron deprivation are I
43 rin suppressed the TNF-induced production of reactive oxygen intermediates and lipid peroxidation.
44                                              Reactive oxygen intermediates and nitric oxide modulate
45  evidence from knock-out mice on the role of reactive oxygen intermediates and reactive nitrogen inte
46                                Resistance to reactive oxygen intermediates and reactive nitrogen inte
47 cally or enzymatically generated halogenated reactive oxygen intermediates and reduced its survival i
48                                              Reactive oxygen intermediates and subsequent oxidative s
49 al cells is independent of the production of reactive oxygen intermediates and that the cytoprotectiv
50 ies of macrophages include the generation of reactive oxygen intermediates and the delivery of bacter
51 ence mechanism against endogenously produced reactive oxygen intermediates and the oxidative stress i
52 l trypanothione reductase system to detoxify reactive oxygen intermediates and to maintain redox home
53 s against the cumulative damaging effects of reactive oxygen intermediates and toxic electrophiles, w
54 nded on the generation of neutrophil-derived reactive oxygen intermediates and was blocked by inhibit
55 reas anti-Fas mAb-induced apoptosis utilizes reactive oxygen intermediates and, in turn, caspase-3 an
56 elevated sensitivity to hydrogen peroxide, a reactive oxygen intermediate, and decreased lung coloniz
57 tempt to establish a linkage between CYP2E1, reactive oxygen intermediates, and ethanol toxicity.
58 tic link between Abeta and the generation of reactive oxygen intermediates, and identify molecular ta
59 ift, serum starvation, increased osmolality, reactive oxygen intermediates, and increased or reduced
60 olysosomal killing mediated by nitric oxide, reactive oxygen intermediates, and L-tryptophan starvati
61 n of small molecules such as salicylic acid, reactive oxygen intermediates, and nitric oxide amplifie
62 ction of inducible nitric oxide synthase and reactive oxygen intermediates, and phagocytose P chabaud
63 violaceum is critically dependent in vivo on reactive oxygen intermediates, and these species are mod
64  integrin-induced adhesion and production of reactive oxygen intermediates, and to a lesser extent, F
65 imal when inducible NO synthase activity and reactive oxygen intermediates are both present.
66  IL-12, reactive nitrogen intermediates, and reactive oxygen intermediates are crucial immune compone
67                          Although oxygen and reactive oxygen intermediates are not required for the e
68 cade, reactive nitrogen intermediates joined reactive oxygen intermediates as a biochemically paralle
69 o the media coincided with the production of reactive oxygen intermediates as demonstrated by the pre
70           These results implicate unquenched reactive oxygen intermediates as the stimulus that initi
71  production of conjugated salicylic acid and reactive oxygen intermediates, as well as spontaneous le
72 the membrane to protect M. tuberculosis from reactive oxygen intermediates at the bacterial surface.
73           SOK-1 is activated 3- to 7-fold by reactive oxygen intermediates, but is not activated by g
74   It is proposed that elevated production of reactive oxygen intermediates by cells expressing CYP2E1
75                      The production of toxic reactive oxygen intermediates by host cells is known to
76 ania-degraded FN decreased the production of reactive oxygen intermediates by parasite-infected macro
77  mechanisms of macrophages are production of reactive oxygen intermediates by phagocyte oxidase (phox
78 nduced IL-6 production is mediated through a reactive oxygen intermediate-dependent pathway.
79 rsensitive response, including generation of reactive oxygen intermediates, deposition of phenolic co
80                                        These reactive oxygen intermediates dissociate from the enzyme
81               Subsequent steps that generate reactive oxygen intermediates diverge and reflect the ef
82 n plays a critical role in the generation of reactive oxygen intermediates during immunity and has be
83 overed are heat-shock proteins, nucleotides, reactive oxygen intermediates, extracellular-matrix brea
84 n kinase C stimulation and the generation of reactive oxygen intermediates for downstream signaling.
85 s responses to signals, possibly mediated by reactive oxygen intermediates from both biotic and abiot
86 in the presence of arginine the formation of reactive oxygen intermediates from NO production by nNOS
87 e electronic states and reaction pathways of reactive oxygen intermediates generated by 77 K radiolyt
88                                              Reactive oxygen intermediates generated by neutrophils k
89                                              Reactive oxygen intermediates generated by the phagocyte
90           Leflunomide suppressed TNF-induced reactive oxygen intermediate generation and lipid peroxi
91                                         Both reactive oxygen intermediate generation and lipid peroxi
92                  SNAP pretreatment inhibited reactive oxygen intermediate generation and lipid peroxi
93                   These results suggest that reactive oxygen intermediate generation, after a brief i
94 te-induced delta psi(m) reduction, secondary reactive oxygen intermediate generation, cardiolipin deg
95 o hypoxia, reoxygenation after hypoxia, or a reactive oxygen intermediate (H(2)O(2)).
96                                          The reactive oxygen intermediate H2O2 can function as a sign
97 nine jugular vein endothelial cells with the reactive oxygen intermediate H2O2 induced a concentratio
98 ular glutathione levels or production of the reactive oxygen intermediate H2O2.
99 ntial (deltapsi(m)) and excess production of reactive oxygen intermediates have been implicated as ke
100                        Both nitric oxide and reactive oxygen intermediates have been implicated in co
101                      The roles of oxygen and reactive oxygen intermediates in apoptosis are unclear a
102 uced cytotoxicity and activated caspases and reactive oxygen intermediates in Jurkat cells but not in
103 nduced cytotoxicity, activated caspases, and reactive oxygen intermediates in Jurkat cells, but not i
104  the capabilities (i.e., oxidizing power) of reactive oxygen intermediates in metalloenzyme chemical
105 rs reduced the killing, indicating a role of reactive oxygen intermediates in the candidacidal activi
106 cells, we examined the role of intracellular reactive oxygen intermediates in the regulation of Fas-m
107  present report, we investigated the role of reactive oxygen intermediates in TNF-induced signaling.
108 ial cells, we showed that pyocyanin-mediated reactive oxygen intermediates inactivate human vacuolar
109 s instead mediated through the generation of reactive oxygen intermediates, inasmuch as preincubation
110                      Use of nitric oxide and reactive oxygen intermediate inhibitors failed to alter
111 tect against the damage of electrophiles and reactive oxygen intermediates is potentially a major str
112  algR mutant was examined for sensitivity to reactive oxygen intermediates, killing by phagocytes, sy
113 role of algU in P. aeruginosa sensitivity to reactive oxygen intermediates, killing by phagocytic cel
114 te did not affect cytosolic or mitochondrial reactive oxygen intermediate levels as monitored by flow
115             Recent observations suggest that reactive oxygen intermediates may play a role in IL-1 an
116         Although it is well established that reactive oxygen intermediates mediate the NF-kappaB acti
117  alter cellular redox state, suggesting that reactive oxygen intermediates might modulate eNOS expres
118 signaling through protein kinase C (PKC) and reactive oxygen intermediates of nonmitochondrial origin
119 e genetically deficient in the production of reactive oxygen intermediates (phox(-/-) mice) were foun
120 ral recently identified signaling molecules, reactive oxygen intermediates play a critical role in ac
121             Recent observations suggest that reactive oxygen intermediates play a role in tumor cell
122  is associated with diminished mitochondrial reactive oxygen intermediate production and Ca(2+) level
123 it significant defects in adhesion-dependent reactive oxygen intermediate production and degranulatio
124 me- and dose-dependent increase in secondary reactive oxygen intermediate production and loss of card
125 nother antioxidant, rotenone, which inhibits reactive oxygen intermediate production by inhibiting th
126 om l/l mice that was associated with reduced reactive oxygen intermediate production in vitro.
127 ess phagocytosis, bactericidal capacity, and reactive oxygen intermediate production, was also increa
128 er extent, FcgammaR-induced calcium flux and reactive oxygen intermediate production.
129 , exhaustion during VL influenced macrophage-reactive oxygen intermediate production.
130 ibited severe defects in MIP-2 secretion and reactive oxygen intermediates production.
131 ted by an oxidation-reduction equilibrium of reactive oxygen intermediates, pyridine nucleotides, and
132  include tumor cell killing, IL-1 secretion, reactive oxygen intermediate release, nitric oxide synth
133 hypoxia is often followed by reperfusion and reactive oxygen intermediate (ROI) generation, we examin
134 tioxidant, was used to perturb intracellular reactive oxygen intermediate (ROI) levels to assess the
135                                Intracellular reactive oxygen intermediate (ROI) levels were increased
136 ants with Bgt resulted in the attenuation of reactive oxygen intermediate (ROI) production and salicy
137                            The importance of reactive oxygen intermediate (ROI) production in antimic
138  decreased FcgammaR-induced calcium flux and reactive oxygen intermediate (ROI) production in respons
139                                Viability and reactive oxygen intermediate (ROI) production were measu
140  in human prostate cancer cells is caused by reactive oxygen intermediate (ROI)-dependent activation
141              These mice are defective in the reactive oxygen intermediate (ROI)-generating phagocyte
142 was estimated by flow cytometric analysis of reactive oxygen intermediate (ROI)-induced 2',7'-dichlor
143 d apoptosis is preceded by 1) an increase in reactive oxygen intermediates (ROI) and 2) an elevation
144 nvestigated the hypothesis that RBC scavenge reactive oxygen intermediates (ROI) and nitric oxide (NO
145 n oxidative burst and the generation of both reactive oxygen intermediates (ROI) and NO.
146 ghtened susceptibility to representatives of reactive oxygen intermediates (ROI) and reactive nitroge
147                                              Reactive oxygen intermediates (ROI) and reactive nitroge
148 e to methionine and protect bacteria against reactive oxygen intermediates (ROI) and reactive nitroge
149 OS2-/-), defective in the production of both reactive oxygen intermediates (ROI) and reactive nitroge
150 ages by cytokines leads to the production of reactive oxygen intermediates (ROI) and reactive nitroge
151      This study examined the contribution of reactive oxygen intermediates (ROI) and reactive nitroge
152  of Mycobacterium bovis (Ravenel and BCG) to reactive oxygen intermediates (ROI) and reactive nitroge
153                                              Reactive oxygen intermediates (ROI) are strongly associa
154                                              Reactive oxygen intermediates (ROI) contribute to neuron
155                                Generation of reactive oxygen intermediates (ROI) following antigen re
156                                              Reactive oxygen intermediates (ROI) generated in respons
157                                              Reactive oxygen intermediates (ROI) generated in respons
158                                              Reactive oxygen intermediates (ROI) have been viewed tra
159 nt study, we have tested the hypothesis that reactive oxygen intermediates (ROI) have the capacity to
160                       The functional role of reactive oxygen intermediates (ROI) in activation-induce
161             Previous studies have implicated reactive oxygen intermediates (ROI) in lymphocyte apopto
162 lecule expression, and limited production of reactive oxygen intermediates (ROI) in response to stimu
163 teine and glutathione, suggesting a role for reactive oxygen intermediates (ROI) in the death process
164           Because recent evidence implicates reactive oxygen intermediates (ROI) in VSMC proliferatio
165 ion, since NADPH oxidase-mediated release of reactive oxygen intermediates (ROI) is a primary bacteri
166 e contributions of respiratory burst-derived reactive oxygen intermediates (ROI) versus reactive nitr
167 to kill tumor cells including TNF-alpha, NO, reactive oxygen intermediates (ROI), and Fas ligand (Fas
168 ugh controlling ATP synthesis, production of reactive oxygen intermediates (ROI), and release of cell
169 uce neutrophil chemotaxis, the generation of reactive oxygen intermediates (ROI), and the production
170 e modification of cellular macromolecules by reactive oxygen intermediates (ROI), often leading to ce
171 vation of several growth factor receptors by reactive oxygen intermediates (ROI).
172 t and in stimulating host cell production of reactive oxygen intermediates (ROI).
173 but reduces the plant's capacity to detoxify reactive oxygen intermediates (ROI).
174 s, and conditions that elevate the levels of reactive oxygen intermediates (ROI).
175 l (Delta psi(m)) and increased production of reactive oxygen intermediates (ROI).
176 ingly, inhibition of bactericidal mediators, reactive oxygen intermediates (ROIs) and reactive nitrog
177 idative mechanisms, but the roles of various reactive oxygen intermediates (ROIs) are not known.
178 res were treated with blue light to generate reactive oxygen intermediates (ROIs) by endogenous retin
179 involves the rapid generation and release of reactive oxygen intermediates (ROIs) by the NADPH oxidas
180 ive burst generating O2- and H2O2, and these reactive oxygen intermediates (ROIs) cue the induction o
181                      Increased production of reactive oxygen intermediates (ROIs) in fibrotic livers
182                                Extracellular reactive oxygen intermediates (ROIs) in plants were prop
183 ate phagocyte-derived superoxide and related reactive oxygen intermediates (ROIs) is the major defect
184                                              Reactive oxygen intermediates (ROIs) play a major role i
185 is is preceded by an exponential increase in reactive oxygen intermediates (ROIs) produced in mitocho
186 chemical mechanism involving ozone-generated reactive oxygen intermediates (ROIs), but not by NO(3) r
187 rane potential (deltapsim) and production of reactive oxygen intermediates (ROIs), mediate the imbala
188 idative burst leading to the accumulation of reactive oxygen intermediates (ROIs), which are thought
189 MV infection of SMCs generates intracellular reactive oxygen intermediates (ROIs).
190 nd, thus, to protect cellular integrity from reactive oxygen intermediates (ROIs).
191 sly exposes them to elevated levels of toxic reactive oxygen intermediates (ROIs).
192  tumor necrosis factor alpha (TNF alpha) and reactive oxygen intermediates (ROIs).
193 bition of nitric oxide synthase, addition of reactive oxygen intermediate scavengers, or the use of a
194 y signaling pathway effectors, as opposed to reactive oxygen intermediates, serve as the first line o
195                   Perhaps species other than reactive oxygen intermediates should be considered as th
196     Nonetheless, these cells did not produce reactive oxygen intermediates, suggesting an inability t
197 athogen triggers the rapid production of the reactive oxygen intermediates superoxide (O2-) and hydro
198 s switch phenotypes, secreted molecules like reactive oxygen intermediates switch impact from pro- to
199 ein increases steady-state concentrations of reactive oxygen intermediates that simulate PKC and decr
200  nitric oxide and a parallel accumulation of reactive oxygen intermediates, the latter generated by N
201  or lower the threshold for its induction by reactive oxygen intermediates, these factors may repress
202 ty of Mycobacterium tuberculosis response to reactive oxygen intermediates, this organism has evolved
203  water requires the formation of metastable, reactive oxygen intermediates to enable oxygen-oxygen bo
204 n the studied seawater by H(2)O(2) and other reactive oxygen intermediates took place at both high an
205                  Mitochondrial generation of reactive oxygen intermediates was necessary and sufficie
206 n that has been shown to reduce synthesis of reactive oxygen intermediates, was activated in the wild
207  a photoinducible intracellular generator of reactive oxygen intermediates, was investigated for comp
208              Using a number of inhibitors of reactive oxygen intermediates we determined that other t
209        Flow cytometry analysis revealed that reactive oxygen intermediates were generated in CPT-trea
210                                              Reactive oxygen intermediates were identified as candida
211           Glomerular mesangial cells produce reactive oxygen intermediates when stimulated by interle
212 ell iron or by upregulating the synthesis of reactive oxygen intermediates (which could potentially r
213 g IL-6 and B cell survival factors, but also reactive oxygen intermediates, which can suppress lympho

 
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