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1 neurodegeneration together with inflammatory oxidative burst.
2 phoid Salmonella by impairing the neutrophil oxidative burst.
3 iveness to flg22, as indicated by a stronger oxidative burst.
4 one marrow with a quantitative defect in the oxidative burst.
5 etween Ca(2+) signaling, metabolism, and the oxidative burst.
6 s essential for EC-K1-mediated inhibition of oxidative burst.
7 mal cytokine production and generation of an oxidative burst.
8 to the amplification of the elicitor-induced oxidative burst.
9 phox) promoter, thereby diminishing the host oxidative burst.
10 east partially susceptible to the neutrophil oxidative burst.
11 on, integrin activation, or induction of the oxidative burst.
12 om PCD that requires the early mitochondrial oxidative burst.
13 g" cells in adhesion stage, without inducing oxidative burst.
14 3 and Rac1 and Rac2 in the FcgammaR-mediated oxidative burst.
15 reducing associated chemokine production and oxidative burst.
16 ated with decreased chemokine production and oxidative burst.
17 ing the plant cell wall and/or triggering an oxidative burst.
18 hway leading to programmed cell death and an oxidative burst.
19 was most efficient in inducing a macrophage oxidative burst.
20 gether completely abrogated the ANCA-induced oxidative burst.
21 process may contribute to the potency of the oxidative burst.
22 ronary dilation and inhibition of neutrophil oxidative burst.
23 ation, including adhesion, phagocytosis, and oxidative burst.
24 ures which might account for its role in the oxidative burst.
25 g was accompanied by an increased macrophage oxidative burst.
26 is correlated with an impaired immature cell oxidative burst.
27 R, placing calcium elevation upstream of the oxidative burst.
28 all middle dot) and ONOO(-) modulate the PMN oxidative burst.
29 vement of Ca2+ in signal transduction of the oxidative burst.
30 in response to pathogens in a process called oxidative burst.
31 lly increase iron levels to activate a toxic oxidative burst.
32 loxanthin production, and sensitivity to the oxidative burst.
33 Monocytes were studied for phagocytosis and oxidative burst.
34 human blood via increased sensitivity to the oxidative burst.
35 la protects itself from damage likely due to oxidative burst.
36 cytosed L. monocytogenes, and have decreased oxidative burst.
37 regulator required for suppressing the host oxidative burst.
38 the site of infection, and displayed blunted oxidative burst.
39 e holoenzyme, resulting in an absence of the oxidative burst.
40 erating cAMP and consequently inhibiting the oxidative burst.
41 c bacterial killing, a process also known as oxidative burst.
42 pathway could be operative in the absence of oxidative burst.
43 y preventing phagocytosis and the associated oxidative burst.
44 acity to prime polymorfonuclear cells for an oxidative burst.
45 which abolishes the NADPH oxidase 2 complex oxidative burst.
47 such as activation of CD11b/CD18 integrins, oxidative burst, actin polymerization, and interaction w
48 ted to those responsible for the respiratory oxidative burst activated in mammalian neutrophils durin
49 ood granulocyte and monocyte phagocytosis or oxidative burst activity after 2.5 h of intensive runnin
53 inant population of neutrophils with reduced oxidative burst activity, which gradually normalized ove
57 evels of SA also potentiate activation of an oxidative burst and a cell death pathway that results in
59 etr1 plants suggested that engagement of the oxidative burst and cognate redox signalling functioned
61 dopsis (Arabidopsis thaliana) leaves induced oxidative burst and expression of PTI early marker genes
62 disrupt other responses, such as the initial oxidative burst and expression of some early defense-ass
63 tant plants display progressively diminished oxidative burst and gene activation induced by the 22-am
64 crobe-associated molecular pattern-triggered oxidative burst and gene expression across four soybean
65 via STIM1/Orai complexes promotes neutrophil oxidative burst and inflammatory gene expression during
66 TIPE2 sets the strengths of phagocytosis and oxidative burst and may be targeted to effectively contr
67 antioxidant enzymes that inhibit neutrophil oxidative burst and negatively modulate platelet aggrega
68 ant (VU-3, Lys to Arg115) to investigate the oxidative burst and nicotinamide co-enzyme fluxes after
71 ole of ABCA1, ABCG1 and HDL in dampening the oxidative burst and preserving viability of macrophages
72 ver, recombinant CD40L stimulated neutrophil oxidative burst and release of matrix metalloproteinase-
73 il the impact of HopM1 on the PAMP-triggered oxidative burst and stomatal immunity in an AtMIN7-indep
74 -3-3 proteins is required for PAMP-triggered oxidative burst and stomatal immunity, and chemical-medi
75 sses two early PAMP-triggered responses, the oxidative burst and stomatal immunity, both of which see
76 tabolic homeostasis, thus quenching the host oxidative burst and suppressing rice innate immunity dur
79 also required for both the elicitor-induced oxidative burst and the transduction of the hydrogen per
80 espectively), to modulate human neutrophils' oxidative burst and to protect Caco-2 cells against oxid
81 roxidase type 1 (FBP1) exhibited an impaired oxidative burst and were more susceptible than wild-type
82 acrophages have an independent defect in the oxidative burst and whether Burkholderia contributes to
84 s responsible for IgA-mediated phagocytosis, oxidative burst, and antibody-dependent cellular cytotox
85 rial internalization, intracellular killing, oxidative burst, and cytokine release during phagocytosi
87 ions to impair human leukocyte phagocytosis, oxidative burst, and extracellular trap production, prom
88 of l-selectin, CD11b upregulation, increased oxidative burst, and faster progression to apoptosis.
89 n-dependent ligand binding, activation of an oxidative burst, and Fc receptor-mediated phagocytosis.
91 nto Opaless Gc, the bacteria induced the PMN oxidative burst, and OpaD(+) Gc survived less well after
92 anule membranes, generating the bactericidal oxidative burst, and releasing lytic enzymes, specific p
94 ype and Ncf1 mutant mice that lack phagocyte oxidative burst, and stimulated with LPS and other agent
95 myristate acetate (PMA), a known promoter of oxidative burst, and the production of superoxide was me
100 ascular rolling and adhesion, migration, and oxidative bursting, are better measured in seconds or mi
102 impaired FcgammaR-mediated phagocytosis and oxidative burst, as well as defective activation of Cdc4
104 Neutrophil functions were assessed using an oxidative burst assay as well as a degranulation assay.
105 study confirms previous reports of a higher oxidative burst associated with AgP and presented prelim
106 nd these macrophages effectively elicited an oxidative burst associated with clearance of Pneumocysti
107 ignificantly decreased the non-mitochondrial oxidative burst associated with inflammatory response in
108 ed defective fungicidal activity and reduced oxidative burst, both of which improved in the presence
109 th 17beta-estradiol demonstrated an enhanced oxidative burst but decreased P. aeruginosa killing and
110 d the ability to phagocytose and generate an oxidative burst, but exhibited defective killing of inte
112 uce a marked transcriptional response and an oxidative burst, but not to cause substantial tissue dam
113 n dictates the strengths of phagocytosis and oxidative burst by binding to and blocking Rac GTPases.
114 Infection of PMNs with EC-K1 suppresses oxidative burst by downregulating rac1, rac2 and gp91(ph
115 P levels, and the inhibition of adhesion and oxidative burst by dPGJ2 was enhanced in the presence of
116 yzed in a masked manner for phagocytosis and oxidative burst by flow cytometry in response to Escheri
117 he discovery of regulatory nodes controlling oxidative burst by functional screening of genes within
118 sitive bacteria by macrophages, induction of oxidative burst by Gram-positive bacteria in neutrophils
121 m TK-/- mice exhibited decreased spontaneous oxidative burst capacity ex vivo, and by intravital micr
122 signaling of CyaA-generated cAMP blocks the oxidative burst capacity of neutrophils by two convergin
124 respect to lymphocyte subsets, phagocytosis, oxidative burst capacity, and T cell proliferation upon
126 e for inherent deficits in the CF macrophage oxidative burst caused by decreased phosphorylation of N
127 itro, including reduced l-selectin shedding, oxidative burst, chemotaxis, neutrophil extracellular tr
129 the development of drugs that generate high oxidative burst could be of great use in tuberculosis tr
133 nhances bacterial clearance, and rescues the oxidative burst defects associated with Ncf4 haploinsuff
134 ently contributes to and worsens the overall oxidative burst deficits in CF MDMs compared with non-CF
136 as Fc-mediated phagocytosis, BCR signaling, oxidative burst, degranulation, cytokine secretion, and
137 elieved to be responsible for the apoplastic oxidative burst demonstrated by suspension-cultured cell
140 a couple of seconds, while higher intensity oxidative bursts due to the emptying of vacuoles outside
141 nthine and urate are produced as part of the oxidative burst during host defenses and under molluscan
142 mechanisms to evade or counter the phagocyte oxidative burst, effectively masking the impact of this
146 ts surface-expressed gp96 in PMNs to prevent oxidative burst for the onset of neonatal meningitis.
148 ition of an avirulent pathogen stimulates an oxidative burst generating O2- and H2O2, and these react
149 tput nitric oxide pathway (iNOS(-/-)) or the oxidative burst (gp91(phox-/-)) are more susceptible to
150 channel blockers prevented expression of the oxidative burst, (ii) introduction of exogenous Ca2+ int
151 n-kinase inhibitors, were found to block the oxidative burst in a concentration-dependent manner.
152 man neutrophil studies, ST94A stimulated the oxidative burst in and adhered to human neutrophils at l
155 Purified CP5 and CP8 stimulated a modest oxidative burst in human neutrophils but failed to activ
156 creas and lung tissues, fMLF peptide-induced oxidative burst in human neutrophils, and cytokine produ
158 ipid dynamics, membrane trafficking, and the oxidative burst in macrophages from SHIP-1-deficient and
159 hil migration, and Fcgamma receptor-mediated oxidative burst in macrophages were decreased in cells f
161 f TF as an important mediator of C5a-induced oxidative burst in neutrophils in aPL-induced fetal inju
162 , fibro-inflammatory responses in PaSCs, and oxidative burst in neutrophils, all cell types participa
163 of O2- and H2O2, which is reminiscent of the oxidative burst in neutrophils, is a central component o
164 is under study for its role in enhancing the oxidative burst in patients with chronic granulomatous d
165 se mutants to inhibit both apoptosis and the oxidative burst in polymorphonuclear leukocytes but were
166 ized that the small GTPase Rac1 mediates the oxidative burst in reperfused tissue and thereby contrib
167 (peroxidase 33 [PRX33] and PRX34), block the oxidative burst in response to a fungal elicitor, and ca
168 ed that patients with AgP exhibited a higher oxidative burst in response to E. coli (P = 0.002) and P
169 educed levels of neutrophil phagocytosis and oxidative burst in response to Escherichia coli stimulat
170 B 19-kDa lipoprotein enhanced the subsequent oxidative burst in response to fMLP as assessed by oxida
172 ssion of AtOXR2 leads to faster and stronger oxidative burst in response to the bacterial flagellin p
173 ox) CYBA 242 T allele was associated with an oxidative burst in response to the challenge by two stra
174 We found that both MAMPs triggered a rapid oxidative burst in root border-like cells of both specie
175 A and okadaic acid) were found to induce the oxidative burst in the absence of any additional stimulu
176 a signal function for Ca2+ downstream of the oxidative burst in the activation of a physiological cel
178 reveals the late and prolonged impact of the oxidative burst in the cytosol that is modified in redox
179 a highly specific TLR4 agonist, elicited an oxidative burst in the monocyte-like cell line THP-1 in
180 ntify cytokine production, phagocytosis, and oxidative burst in the presence or absence of blocking a
181 s the early role of the neutrophil and of an oxidative burst in this infection with an intracellular
182 crease adherence, migration, chemotaxis, and oxidative burst in vitro, and primes monocyte response t
184 ulent Pseudomonas syringae induces secondary oxidative bursts in discrete cells in distant tissues, l
185 strated improved neutrophil function: normal oxidative burst (in 3 of 3 patients tested), corrected p
186 ytic activity was decreased, and spontaneous oxidative burst increased in all patients with acetamino
187 S and opsonized with the same sera using the oxidative burst indicator system dihydrorhodamine123/rho
188 inhibitor bisindolylmaleimide inhibited the oxidative burst induced by either PMA or intact pseudomo
192 to those elicited by flagellin, including an oxidative burst, induction of defense-response genes, an
193 ious effect of cellular damage caused by the oxidative burst inside the macrophages, C. neoformans ha
203 f avirulent microbial pathogens activates an oxidative burst leading to the accumulation of reactive
204 GmMMP2 activation did not correlate with the oxidative burst leading to the hypersensitive response c
205 ERK-MAPK pathway, CREB, and generation of an oxidative burst, leading to downstream production of IL-
207 activity as measured by phagocytic activity, oxidative burst, lysozyme secretion, and ability to limi
208 production is one of the first indicators of oxidative burst, macrophage cells were exposed within th
209 ponse that should not require PPARgamma, the oxidative burst made by adherent human neutrophils.
210 H oxidase 2 complex that mediates neutrophil oxidative burst, markedly reduced CXCL1-induced NASH and
212 ge pathogen-like Leishmania is inhibition of oxidative burst-mediated macrophage apoptosis to protect
213 in (thioredoxin reductase inhibitor) induces oxidative burst, mitochondrial damage, and necrotic cell
214 and tissue bacterial burdens, and neutrophil oxidative burst), morphologic (i.e., liver histology and
215 anate-labeled opsonized Escherichia coli and oxidative burst (OB) was determined by the percentage of
218 xide were simultaneously detected during the oxidative burst of a zymosan-stimulated macrophage cell.
219 This species is also generated during the oxidative burst of activated human neutrophils and durin
221 um have been reported to protect against the oxidative burst of host innate immune cells using a fami
222 odestly increased phagocytosis/killing by an oxidative burst of murine neutrophils in vitro Intravita
223 O(2) production by lactic acid bacteria, the oxidative burst of phagocytes and the redox-cycling of s
225 dogenous H2O2 in cell culture to monitor the oxidative burst of promyelocytes and in vivo to image lu
228 on of these variants in cells either reduced oxidative burst or altered interactions among proteins i
229 mutant is lost upon inhibition of neutrophil oxidative burst or in human or murine nicotinamide adeni
231 ant goal and molecular identification of the oxidative burst peroxidase allows further exploration of
232 ignificant reduction in Fc receptor-mediated oxidative burst, phagocytosis of opsonised polystyrene b
233 Recent findings indicate that H2O2 from this oxidative burst plays a central role in the orchestratio
234 ta demonstrate that the peroxidase-dependent oxidative burst plays an important role in Arabidopsis b
235 Neutrophil functions, such as phagocytosis, oxidative burst, polarization, and chemotaxis, were augm
236 iva, Sinorhizobium meliloti must overcome an oxidative burst produced by the plant in order for prope
238 toneal neutrophil recruitment with increased oxidative burst production, whereas the TLR7/8 agonist a
239 ated murine peritoneal macrophages producing oxidative burst products but is unaffected by macrophage
240 to the resistance of M. tuberculosis against oxidative burst products generated by activated macropha
241 so include those with a putative role in the oxidative burst, proteolysis, the hypersensitive respons
242 ic ingestion and initiation of intracellular oxidative burst (r(2) = 0.99) using polystyrene beads co
243 activate many defense responses including an oxidative burst, rapid changes in the expression of over
246 Major PMN effector mechanisms, including oxidative burst, release of secondary granule contents a
247 e, tissue damage-associated component of the oxidative burst requires only the Galpha protein and ari
248 MAPKAP kinase 2 in neutrophil function, the oxidative burst response after manipulation of endogenou
250 estingly, a stimulus-dependent defect in the oxidative burst response of LFKO neutrophils was observe
253 estin, which is protection from an excessive oxidative burst, resulting from the sustained stimulatio
254 poptotic cells was dependent on an excessive oxidative burst secondary to enhanced assembly of NADPH
255 ioning in direct defense, defense signaling, oxidative burst, secondary metabolism, abiotic stress, c
256 NA damage response, like deficiencies in the oxidative burst seen in chronic granulomatous disease, c
258 abscisic acid, salicylic acid, ethylene, and oxidative burst signaling) and in reactive oxygen metabo
259 pulses are essential to transduction of the oxidative burst signals by their respective elicitors: (
260 t of the signal transduction pathway linking oxidative burst signals to diverse downstream responses.
262 sis were significantly more resistant to the oxidative burst than wild-type bacteria in human blood o
263 cient neutrophils displayed a very transient oxidative burst that abruptly ceased shortly after stimu
264 e that plastid genome instability induces an oxidative burst that favors, through nuclear genetic rep
265 rkedly up-regulated in PC in response to the oxidative burst that follows PC-GB cell interaction.
266 diphenylene iodonium-insensitive apoplastic oxidative burst that generates H(2)O(2) in response to a
268 f the roots caused by harvesting triggers an oxidative burst that spreads throughout the cassava root
270 ukocytes, G(vH+) are required to support the oxidative burst that underlies microbial killing by the
272 ctivate PKCdelta and induction of neutrophil oxidative burst, the current study shows that the potent
274 r own NO as a key defense against the immune oxidative burst, thereby establishing bNOS as an essenti
275 te that phagosomal SHIP-1 enhances the early oxidative burst through localized alteration of the memb
276 We have investigated the source of this oxidative burst to identify possible strategies to limit
278 novel applications using blue light induced oxidative bursts to prime crop plants against the delete
279 Downstream responses include ion fluxes, an oxidative burst, transcriptional reprogramming, and, in
283 -type neutrophils that exhibited a sustained oxidative burst upon stimulation with phorbol ester and
284 owever, monocyte phagocytosis was normal and oxidative burst was augmented, suggesting that their inn
287 ylococcal killing was normal, and neutrophil oxidative burst was increased both basally and on stimul
288 ymorphonuclear neutrophils; induction of the oxidative burst was inhibited by antibodies to either CD
291 ependent adhesion and the adhesion-dependent oxidative burst was tested using a specific inhibitor of
292 5-oxo-ETE, except ERK1/2 phosphorylation and oxidative burst, were likewise prevented by pertussis to
293 s to yield up to a 50-fold increase in their oxidative burst when elicited in vitro with phorbol myri
296 successful detection of sustained macrophage oxidative burst, which corresponds to an increase in the
297 nhibitor also blocked the adhesion-dependent oxidative burst with a half-maximal concentration simila
298 n early transient rise in SA potentiates the oxidative burst, with resultant effects on accumulation
300 ac1N17) partially suppressed the TNF-induced oxidative burst without affecting TNF-induced mitochondr