ライフサイエンスコーパス: neutrophil infiltration

1 ered in disease models, in part, by reducing neutrophil infiltration.

2 ere pancreatic injury including necrosis and neutrophil infiltration.

3 to worsened intestinal damage and increased neutrophil infiltration.

4 of disease, including AHR and macrophage and neutrophil infiltration.

5 l catheterization, rarely showed evidence of neutrophil infiltration.

6 uced apoptosis, reactive oxygen species, and neutrophil infiltration.

7 ammatory disorders that are characterized by neutrophil infiltration.

8 late phase that is associated with enhanced neutrophil infiltration.

9 ing both proinflammatory cytokine levels and neutrophil infiltration.

10 of increased vascular permeability and early neutrophil infiltration.

11 ce of membrane attack complex activation and neutrophil infiltration.

12 d CD8(+) T cells, and reduces macrophage and neutrophil infiltration.

13 dendritic cells and significantly suppressed neutrophil infiltration.

14 cted animals through 24 h, as was peritoneal neutrophil infiltration.

15 tion model, where they caused a reduction in neutrophil infiltration.

16 nd systemically, but was not associated with neutrophil infiltration.

17 mor foci due to tumor development-associated neutrophil infiltration.

18 ntitumor immune response by inducing massive neutrophil infiltration.

19 levels, reduced hepatic necrosis, and lower neutrophil infiltration.

20 e of epithelial erosions, corneal edema, and neutrophil infiltration.

21 n adipose tissue endothelial cells to induce neutrophil infiltration.

22 eroxidase (MPO) assay was used to quantitate neutrophil infiltration.

23 elated with activation of mTOR signaling and neutrophil infiltration.

24 as interleukin-6 and bronchoalveolar lavage neutrophil infiltration.

25 h Th17-induced pathology, nor did it prevent neutrophil infiltration.

26 id TM may be caused by the early increase in neutrophil infiltration.

27 ogical findings of epidermal hyperplasia and neutrophil infiltration.

28 o model of acute lung injury associated with neutrophil infiltration.

29 ed in preterm birth and are characterized by neutrophil infiltration.

30 chemokine secretion from lung, but impairing neutrophil infiltration.

31 red wine significantly reduced post-ischemic neutrophil infiltration.

32 through a mechanism that involved increased neutrophil infiltration.

33 epidermal hyperproliferation, and increased neutrophil infiltration.

34 interleukin-1beta (IL-1beta), which sustains neutrophil infiltration.

35 s for use in inflammatory diseases involving neutrophil infiltration.

36 neutrophil [7/4] antigen, indicating reduced neutrophil infiltration.

37 tion, decreased epidermal proliferation, and neutrophil infiltration.

38 s, which did not affect cytokine release and neutrophil infiltration.

39 duced bone marrow granulopoiesis and cardiac neutrophil infiltration 3 days after MI.

40 elayed corneal healing (13.2%) and increased neutrophil infiltration (54.1%) by day 4 in WT mice, whe

41 mokine ligand 1 (CXCL1), a key chemokine for neutrophil infiltration (a hallmark of NASH), is highly

42 onal location of the bacterial infection and neutrophil infiltration, a diffuse optical tomography re

43 Unexpectedly, myocardial infarct size and neutrophil infiltration/activity 2 days after AMI were a

44 NPD1 decreased neutrophil infiltration after 2 and 4 days of treatment.

45 IL-22 also played a major role in neutrophil infiltration after imiquimod treatment.

46 talk in the outer medulla and in suppressing neutrophil infiltration after kidney injury.

47 dial capillary fractional area and decreased neutrophil infiltration after MI.

48 lts from airway damage, mucosal dysfunction, neutrophil infiltration, airway coagulopathy with cast f

49 Only the old mice developed airway neutrophil infiltration and a Th17 immune response upon

50 kin inflammation characterized by T cell and neutrophil infiltration and a Th17-biased cytokine respo

51 tubular injury, IgG and C4d deposition, and neutrophil infiltration and activation.

52 This strain induced higher levels of neutrophil infiltration and caused smaller lesions than

53 d persistent increased ACE2 activity reduces neutrophil infiltration and compromises host defense, le

54 Airway neutrophil infiltration and CXCL1 (KC) expression were a

55 This was accompanied by a decrease in neutrophil infiltration and cytokine levels.

56 ong inflammatory responses in the lungs with neutrophil infiltration and edema, further confirmed as

57 found that consumption of an HFD resulted in neutrophil infiltration and enhanced MPO expression and

58 ng artery ligation model, as well as reduced neutrophil infiltration and fibrosis.

59 ented the onset of meningitis and suppressed neutrophil infiltration and glial cell migration in the

60 inoculum (1 x 10(7) CFU) of BG2 caused less neutrophil infiltration and greater burdens in peritonea

61 wed significantly higher levels of pulmonary neutrophil infiltration and higher amounts of pulmonary

62 nd responded to the infection with extensive neutrophil infiltration and histopathological changes in

63 of either IL-17A or IL-22 reduced T cell and neutrophil infiltration and host defense peptide elabora

64 aneous periodontitis that featured excessive neutrophil infiltration and IL-17 expression; disease wa

65 sive pulmonary inflammation characterized by neutrophil infiltration and IL-17 response with increase

66 NDV-3 induced increases in CD3+ T-cell and neutrophil infiltration and IL-17A, IL-22, and host defe

67 the adult epicardium reduced injury-induced neutrophil infiltration and improved cardiac function.

68 trans expression of SsE(M28) in GAS reduced neutrophil infiltration and increased skin invasion in s

69 modeling and IL8 gene expression, leading to neutrophil infiltration and inflammation.

70 -selectin plays an important role in hepatic neutrophil infiltration and injury induced by chronic-bi

71 ive effect on anti-MHC induced IL-8-mediated neutrophil infiltration and innate immune responses that

72 oth acute lung injury groups as evidenced by neutrophil infiltration and levels of cytokines in bronc

73 lpha antibodies also significantly prevented neutrophil infiltration and liver injury.

74 IL-17 secretion then leads to neutrophil infiltration and lung epithelial changes, in

75 s involved, we discovered that ACE2 inhibits neutrophil infiltration and lung inflammation by limitin

76 These effects were associated with reduced neutrophil infiltration and macrophage accumulation and

77 atment significantly reduced lymphocytic and neutrophil infiltration and mast cells degranulation (p

78 ced thrombus burden, with significantly less neutrophil infiltration and more proresolving monocytes

79 ly larger infarcts concordant with increased neutrophil infiltration and myocyte apoptosis compared w

80 etwork of inflammatory mediators that induce neutrophil infiltration and NET formation responsible fo

81 and exacerbated stroke injury by aggravating neutrophil infiltration and neurodegeneration in vivo.

82 k disassembly was accompanied by decrease in neutrophil infiltration and neutrophil extracellular tra

83 ared with antibiotics and is associated with neutrophil infiltration and PGD.

84 lar surface tissues, including elevated Gr1+ neutrophil infiltration and proinflammatory cytokines/ch

85 with a 54% decrease (p < 0.05) in pulmonary neutrophil infiltration and reduced alveolar wall thicke

86 also resolved E. coli infections by limiting neutrophil infiltration and stimulating bacterial phagoc

87 ate the importance of MFG-E8 in ameliorating neutrophil infiltration and suggest MFG-E8 as a novel th

88 Administration of DNase I to mice reduced neutrophil infiltration and tissue damage in the inflame

89 Human NASH features hepatic neutrophil infiltration and up-regulation of major neutr

90 Neutrophil infiltration and upregulation of expression o

91 ibrosis, 0.86 for bilirubinostasis, 0.60 for neutrophil infiltration, and 0.46 for megamitochondria.

92 icant reduction in MMP-9/-3, less peripheral neutrophil infiltration, and a preservation of tight jun

93 less intense cytokine responses, diminished neutrophil infiltration, and accelerated uroepithelial r

94 o and triggered multiple cytokine responses, neutrophil infiltration, and acute inflammatory histopat

95 ED1 monocytes and macrophages, and pulmonary neutrophil infiltration, and also enhanced the accumulat

96 NPCT; reduced lung inflammation and injury, neutrophil infiltration, and bacterial invasion; and imp

97 imaging, clinical scoring, bacterial burden, neutrophil infiltration, and CXCL2 expression.

98 The bronchial termini had robust neutrophil infiltration, and depletion of neutrophils ab

99 eduction of microvascular hyperpermeability, neutrophil infiltration, and endothelial adhesion molecu

100 molecule-1 expression, reduced intima/media neutrophil infiltration, and increased DHCR24 and HO-1 m

101 exacerbated hepatocyte necrosis, apoptosis, neutrophil infiltration, and inflammatory cytokine gener

102 farct, demyelination, P-selectin expression, neutrophil infiltration, and microthrombi formation.

103 ed significantly higher cytokine production, neutrophil infiltration, and more rapid fungal clearance

104 xhibited significantly reduced infarct size, neutrophil infiltration, and myocyte apoptosis compared

105 Infarct size, neutrophil infiltration, and myocyte apoptosis in the le

106 otin-dUTP nick end-labeling)-positive cells, neutrophil infiltration, and proinflammatory mRNAs as we

107 layed significantly attenuated inflammation, neutrophil infiltration, and reduced severity of oviduct

108 rine model of sterile kidney injury, reduced neutrophil infiltration, and serum creatinine levels wer

109 ansaminases, histological signs of necrosis, neutrophil infiltration, and serum levels of interleukin

110 opic signs of colon inflammation, macrophage/neutrophil infiltration, and the expression of proinflam

111 an increase in plasma nucleosomes, abundant neutrophil infiltration, and the presence of citrullinat

112 Hepatocyte death is amplified by liver neutrophil infiltration, and the release of necrotic pro

113 assessing necrosis, platelet deposition, and neutrophil infiltration, and the status of steatosis aft

114 oviducts and uterine horns exhibited reduced neutrophil infiltration, and this reduction persisted af

115 and sepsis-induced ALI abolished lung edema, neutrophil infiltration, and tissue damage, thereby reve

116 istones, suppressed intrarenal inflammation, neutrophil infiltration, and tubular cell necrosis and i

117 intercellular adhesion molecule expression, neutrophil infiltration, and vascular leakage.

118 Serum interleukin-8 (IL-8) levels and tumor neutrophil infiltration are associated with worse progno

119 In conclusion, IL-8 production and neutrophil infiltration are increased in a high-glucose

120 vented chronic-binge ethanol-induced hepatic neutrophil infiltration as well as elevation of serum tr

121 d mice exhibited significantly more airspace neutrophil infiltration at 6 hours following P. aerugino

122 MGAS2221 induced robust neutrophil infiltration at the edge of skin infection si

123 lity, which could be associated with reduced neutrophil infiltration at the infectious foci, increase

124 Histologically, DR was associated with neutrophil infiltration at the periportal area.

125 ctant-1 in the systemic circulation enhanced neutrophil infiltration, BBB permeability, and injury.

126 Increased EAE severity and neutrophil infiltration because of Del-1-deficiency was

127 Pulmonary neutrophil infiltration, biomechanical function, and res

128 bone destruction, with significantly reduced neutrophil infiltration but considerably more macrophage

129 at IL-36gamma specifically induces transient neutrophil infiltration but does not impact monocyte and

130 ltured endothelial cells while reducing lung neutrophil infiltration by 40% in a mouse model of LPS-i

131 accumulated into the liver, and blockage of neutrophil infiltration by anti-granulocyte receptor 1 d

132 and induced models of colitis by regulating neutrophil infiltration, colitogenic CD4(+) T cell activ

133 is and apoptosis in the parenchyma and fewer neutrophil infiltration compared to CS liver tissues.

134 o-inflammatory cytokine responses and reduce neutrophil infiltration compared with a PLY mutant.

135 cted STAT1/IL-13 DKO mice also had increased neutrophil infiltration compared with that of RSV-infect

136 Neutrophil infiltration constitutes the first step in wo

137 e dismutase, nitric oxide, heme oxygenase-1, neutrophil infiltration, cysteamine, mucin, hydrogen sul

138 the immune response, including reduction of neutrophil infiltration, decreased T cell cytokine produ

139 ased mortality that correlated with elevated neutrophil infiltration, diminished numbers of mature ol

140 her levels of reactive oxygen species (ROS), neutrophil infiltration, dityrosine and 4-HNE, as well a

141 ed to reveal MFG-E8 roles in regulating lung neutrophil infiltration during ALI.

142 th high HIC index values (0.88-0.96) induced neutrophil infiltration, elevation of pro-inflammatory c

143 ase was associated with increased intestinal neutrophil infiltration, epithelial injury, and permeabi

144 increased epidermal thickness, mast cell and neutrophil infiltration, expression of inflammatory medi

145 damage, 4-hydroxynanoneal adduct formation, neutrophil infiltration, fibrosis, and microvascular pru

146 response by releasing IL-1beta and promoting neutrophil infiltration following ICH.

147 le in the disease have long been recognized, neutrophil infiltration has also been assessed in many c

148 nted oxidative stress, NF-kappaB activation, neutrophil infiltration, hepatocyte apoptosis, and liver

149 ysteine also prevented NF-kappaB activation, neutrophil infiltration, hepatocyte apoptosis, and liver

150 neys, cytokine and chemokine storm, striking neutrophil infiltration, histological abnormalities in b

151 Additionally, higher neutrophil infiltration, IL-17 expression, and intestina

152 Bacterial loads, MODS, leukopenia, neutrophil infiltration, immune cell activation, circula

153 205 reduced disease activity index score and neutrophil infiltration in a mouse dextran sodium sulfat

154 iphenylmethane (4MDM) promoted resolution of neutrophil infiltration in a murine cigarette smoke-indu

155 n of EC Notch signaling inhibited peritoneal neutrophil infiltration in an ovarian carcinoma mouse mo

156 indices, paw thickness, cartilage damage and neutrophil infiltration in both CIA and CAIA models.

157 trant significantly inhibited macrophage and neutrophil infiltration in both models.

158 e treatment inhibited hepatic macrophage and neutrophil infiltration in CCl4 -induced hepatitis and s

159 As anticipated, postischemic neutrophil infiltration in CD36(-/-) -->CD36(-/-) mice w

160 sion, blood-brain barrier (BBB) leakage, and neutrophil infiltration in damaged white matter.

161 recruited type 2 macrophages, and prevented neutrophil infiltration in diabetic wounded corneas.

162 utic N-acetylcysteine lowers gastric mucosal neutrophil infiltration in H. pylori-infected Le(b)-expr

163 e, neuronal cell death, oedema formation and neutrophil infiltration in H/I mice.

164 appaB activation established a link to favor neutrophil infiltration in inducing liver damage during

165 immunostaining showed a dramatic decrease of neutrophil infiltration in infected lung tissues for lin

166 gic improvement (defined as the composite of neutrophil infiltration in less than 5% of crypts and no

167 rophil recruitment based on the reduction of neutrophil infiltration in mice in which the overall sul

168 IL-15DeltaE7 also profoundly blocked neutrophil infiltration in SDS- or immiquimod (IMQ)-trea

169 To corroborate these findings in vivo, neutrophil infiltration in self-limited peritonitis was

170 Increased neutrophil infiltration in Splunc1 KO mice was accompani

171 tic target for the restriction of pathogenic neutrophil infiltration in TH17-mediated autoimmune dise

172 ed NF-kappaB nuclear staining, and decreased neutrophil infiltration in the cecum.

173 d IL-17-producing CD4(+) T cells, as well as neutrophil infiltration in the cornea.

174 owed deeper bacterial penetration and denser neutrophil infiltration in the dermis.

175 crophages and IL-17A produced in situ drives neutrophil infiltration in the epidermis and dermis of t

176 ke skin model, we show that KO mice had less neutrophil infiltration in the epidermis than controls,

177 ng to either insufficient MDSCs or excessive neutrophil infiltration in the fetomaternal interface ma

178 , UFP ingested mice developed macrophage and neutrophil infiltration in the intestinal villi, accompa

179 e-blood levels of QSOX1 and PLBD1 related to neutrophil infiltration in the ischemic myocardium in an

180 Anxa2(-/-) mice develop pulmonary edema and neutrophil infiltration in the lung parenchyma in respon

181 However, thrombin did contribute to neutrophil infiltration in the lung, independently of PA

182 APC, more interleukin-6, and show increased neutrophil infiltration in the lungs compared with WT co

183 Histochemical staining revealed that neutrophil infiltration in the lungs occurred in two wav

184 male OVA-specific TH17 cells increased acute neutrophil infiltration in the lungs of OVA-challenged r

185 ation of pro-inflammatory cytokines, reduced neutrophil infiltration in the lungs, and diminished hep

186 k EhMIF had reduced chemokine expression and neutrophil infiltration in the mucosa.

187 sed alveolar bone loss and a lower degree of neutrophil infiltration in the periodontium than vehicle

188 rization, fibrin depositions, macrophage and neutrophil infiltration in the placenta did not differ b

189 munohistochemistry revealed comparable early neutrophil infiltration in the renal cortex from P2X(7)(

190 ntent, and can be used as a marker to assess neutrophil infiltration in the tissue.

191 ction in active glomerular proliferation and neutrophil infiltration in three of five patients, consi

192 ast cell-derived TNF, as we observed reduced neutrophil infiltration in W(sh)/W(sh) mice reconstitute

193 lation by CL 316,243 promotes adipose tissue neutrophil infiltration in wild type and P-selectin-null

194 To sort out the role of adipose neutrophil infiltration independent of cPLA2alpha induct

195 o WT LTx, with enhanced hepatic necrosis and neutrophil infiltration, indicating a protective role of

196 tor GM6001 reduced the early BBB leakage and neutrophil infiltration, indicating that OPC-derived MMP

197 Ps (NPs-CD11b) into the tumor is mediated by neutrophil infiltration induced by photosensitization (P

198 effectively prevented cPLA2alpha induction, neutrophil infiltration into adipose tissue (likely invo

199 2 receptor and is characterized by extensive neutrophil infiltration into different organs, including

200 Three days after ligation, neutrophil infiltration into ischemic limbs of AMPKalpha

201 Mice lacking IFN-beta had increased neutrophil infiltration into musculoskeletal tissues, an

202 However, the presence of neutrophil infiltration into sterile injuries (in the ab

203 LPS and BTH also induced neutrophil infiltration into the air pouch, which was no

204 duce either cytokine/chemokine production or neutrophil infiltration into the air pouch.

205 nhibit some aspects of inflammation, such as neutrophil infiltration into the air pouch.

206 tic fibrosis, are characterized by excessive neutrophil infiltration into the airspace.

207 lung inflammation, as evidenced by a reduced neutrophil infiltration into the airways, with diminishe

208 1(-/-)) exhibited a significant reduction in neutrophil infiltration into the brain after TBI as comp

209 Kinetic studies demonstrate that neutrophil infiltration into the cerebellum and brainste

210 S3(fl/fl) mice is characterized by extensive neutrophil infiltration into the cerebellum and brainste

211 iorates atypical EAE development by reducing neutrophil infiltration into the cerebellum/brainstem.

212 ed keratinocyte activation and inhibition of neutrophil infiltration into the dermis, demonstrating t

213 s characterized by epithelial extrusions and neutrophil infiltration into the fin.

214 l, Cj-P1 induced more C. jejuni invasion and neutrophil infiltration into the Il10(-/-) mouse colon t

215 rdination, and working memory, and abrogated neutrophil infiltration into the injured brain.

216 ngth accompanied by prominent macrophage and neutrophil infiltration into the intestinal villi, admin

217 enzymes, focal ischaemic areas and a robust neutrophil infiltration into the liver.

218 -type activated PC and significantly reduced neutrophil infiltration into the lungs of septic mice.

219 way wall thickness as well as eosinophil and neutrophil infiltration into the respiratory airway.

220 CHS requires prior CXCL1- and CXCL2-mediated neutrophil infiltration into the site.

221 epidermis are associated with macrophage and neutrophil infiltration into the tissues.

222 Preventing Ly6Clo monocyte or Ly6G+ neutrophil infiltration into tumors enhanced inhibition

223 the tumor associated molecules that regulate neutrophil infiltration into tumors may provide new and

224 Neutrophil infiltration is a hallmark of nonalcoholic st

225 enous myeloperoxidase infusion revealed that neutrophil infiltration is a prerequisite for myocardial

226 ted with diabetic wounds, while reduction of neutrophil infiltration is associated with enhanced heal

227 Collectively, these data show that decidual neutrophil infiltration is not essential for the inducti

228 tigated the role of VEGF165b in brain edema, neutrophil infiltration, ischemic brain damage, and neur

229 eover, while the absence of IL-1R1 prevented neutrophil infiltration, it did not protect from acantho

230 rrier that results in edema, hemorrhage, and neutrophil infiltration, leading to exacerbated lung inf

231 ion (STAT)6 ameliorated alpha-Galcer-induced neutrophil infiltration, liver injury, and hepatitis.

232 ion including epithelial damage, congestion, neutrophil infiltration, loss of mucin from goblet cells

233 flammation signature was linked to increased neutrophil infiltration, more cell death and greater par

234 a), neutrophil chemoattractants (MIP-2, KC), neutrophil infiltration (MPO activity), lipid peroxidati

235 33, IL-17alpha, IL-2, MIP-2, and MCP-1), and neutrophil infiltration (myeloperoxidase staining)).

236 ministration of recombinant IL-17A increased neutrophil infiltration, NET formation, and liver necros

237 se PAR1 is expressed at sites where abundant neutrophil infiltration occurs, we hypothesized that neu

238 TREM-1/3-deficient lungs revealed decreased neutrophil infiltration of the airways.

239 ILC depletion was associated with neutrophil infiltration of the gut lamina propria, type

240 We analyzed neutrophil infiltration of the mouse ileum after allo-HC

241 posome treatment, translating into a massive neutrophil infiltration of the peritoneum capable of neu

242 Neutrophil infiltration of the uteroplacental tissues ha

243 The dermal neutrophil infiltration of the wound, as represented by

244 classical hallmark of acute inflammation is neutrophil infiltration of tissues, a multistep process

245 only develop fatty liver without significant neutrophil infiltration or elevation of chemokines.

246 ssed AHR and failed to dampen macrophage and neutrophil infiltration or inflammatory cytokine product

247 erestingly, mice with neutropenia, defective neutrophil infiltration or lacking elastase were protect

248 NASH progression in HFD-fed mice by inducing neutrophil infiltration, oxidative stress, and stress ki

249 y lymph (p < 0.01 at 24 and 48 hr), alveolar neutrophil infiltration (p = 0.04), and pulmonary myelop

250 s are the main cause of ALI, leading to lung neutrophil infiltration, permeability increases, deterio

251 nalyzed for morphological injury, apoptosis, neutrophil infiltration, proinflammatory mRNAs, and TGF-

252 Passive immunization with 2B11 increased neutrophil infiltration, reduced skin invasion, and prot

253 vestigated whether NLRP3 knockdown decreases neutrophil infiltration, reduces brain edema, and improv

254 gulated 10-fold, whereas expression of other neutrophil infiltration-related adhesion molecules (e.g.

255 Neutrophil infiltration remained low in acutely injured

256 Neutrophil infiltration represents the early acute infla

257 on in vivo abrogated alcohol-induced hepatic neutrophil infiltration, resident immune cell activation

258 Enhanced neutrophil infiltration resulted in part from reduced ro

259 same time, inflammasome activation enhances neutrophil infiltration, resulting in inflammation.

260 to establish a functional link between lung neutrophil infiltration, secretion of chemokines by canc

261 rthermore, platelet depletion abrogated lung neutrophil infiltration, suggesting a sequential partici

262 MCC950 significantly reduced neutrophil infiltration, T-cell activation, and disease

263 n induced greater necrotic airway damage and neutrophil infiltration than A2 infection.

264 e using photosensitization rapidly activates neutrophil infiltration that mediates delivery of nanoth

265 ranscription of c-Myb and elevated levels of neutrophil infiltration, thereby alleviating infectious

266 This phenotype correlates with reduced neutrophil infiltration to both the primary tumour and m

267 pathway and production of CXC chemokines and neutrophil infiltration to infected tissues.

268 Neutrophil infiltration to ischemic tissues following re

269 jury, selective deletion of EC MIF decreases neutrophil infiltration to the bronchoalveolar lavage an

270 gulation of nitric oxide and upregulation of neutrophil infiltration to the infarct area.

271 d chemokine levels, as well as a decrease in neutrophil infiltration to the liver.

272 hibitor of IKK-2, resulted in suppression of neutrophil infiltration to the lung tissues and reductio

273 Excessive neutrophil infiltration to the lungs is a hallmark of ac

274 /W(sh) mice, respond to IL-33 treatment with neutrophil infiltration to the peritoneum, whereas other

275 roduction by gammadelta T cells and ILC3 and neutrophil infiltration to the site of infection, were g

276 Neutrophil infiltration to the sites of mucosal Candida

277 CO92 Deltapgm infections, with an increased neutrophil infiltration to the spleen 5 days postinfecti

278 This promoted neutrophil infiltration, tumor cell (TC) adhesion to the

279 matory state in endothelial cells, promoting neutrophil infiltration, tumor cell adhesion, and metast

280 The degree of fibrosis, degree of neutrophil infiltration, type of bilirubinostasis, and p

281 reflow injury, promoting repair via limiting neutrophil infiltration, up-regulating Ki67, and Roof pl

282 e destruction, bacterial invasion, increased neutrophil infiltration, upregulation of cytokines inclu

283 Reduction of cardiac permeability and neutrophil infiltration was also observed in P2Y4-null m

284 Significant inhibition of neutrophil infiltration was also observed in the WA grou

285 The I/R-evoked neutrophil infiltration was also suppressed in Tg hearts

286 regulated in CSF-1-deficient RT2 tumors, and neutrophil infiltration was increased.

287 nd chemokines was the same as LPS alone, but neutrophil infiltration was inhibited, likely by interru

288 D36(-/-) mice, in which infarcts were small, neutrophil infiltration was large and similar to that of

289 By contrast, neutrophil infiltration was more variable and delayed, c

290 A 100-fold reduction in neutrophil infiltration was observed in the lungs of the

291 Massive neutrophil infiltration was observed in the spleen and l

292 eutrophil recruitment to the brain, and that neutrophil infiltration was required for parenchymal tis

293 CSF3R expression, a neutrophil signature and neutrophil infiltration were associated with a type 1 im

294 okines/chemokines, microglial activation and neutrophil infiltration were evaluated.

295 Apoptosis and neutrophil infiltration were increased in the pancreas o

296 ithelial permeability, muscle thickness, and neutrophil infiltration were studied in colon tissues an

297 male mice, which had hepatic lymphocyte and neutrophil infiltration, were treated by vancomycin, pol

298 nts, albuminuria, serum urea, and glomerular neutrophil infiltration when compared with WT littermate

299 ase of inflammation-(d1), 15-epi-LXA4 primes neutrophil infiltration with a robust increase of Ccl2 a

300 This effectively prevented neutrophil infiltration without affecting cPLA2alpha or