ライフサイエンスコーパス: polymorphonuclear neutrophil

1 ctively inhibited CXCL8-induced migration of polymorphonuclear neutrophils.

2 citation reduces tissue damage by inhibiting polymorphonuclear neutrophils.

3 ion was studied in vitro with isolated human polymorphonuclear neutrophils.

4 kin-10 (IL-10) and can inhibit chemotaxis of polymorphonuclear neutrophils.

5 ith the C5a receptor on many cells including polymorphonuclear neutrophils.

6 ther cationic peptides, serum complement, or polymorphonuclear neutrophils.

7 sonophagocytosis and killing of GAS by human polymorphonuclear neutrophils.

8 ctivation of the integrin alpha(M)beta(2) on polymorphonuclear neutrophils.

9 nership between uPAR and L-selectin in human polymorphonuclear neutrophils.

10 ithelial corneal infiltrates are composed of polymorphonuclear neutrophils.

11 ering mediates activation signaling in human polymorphonuclear neutrophils.

12 sis in children was associated with elevated polymorphonuclear neutrophils.

13 profile and impaired antifungal activity of polymorphonuclear neutrophils.

14 rs (degree of fibrosis) and concentration of polymorphonuclear neutrophils.

15 ollagenase thought to be expressed mainly by polymorphonuclear neutrophils.

16 is and reactive oxygen species generation in polymorphonuclear neutrophils.

17 hrough its actions on gammadelta-T cells and polymorphonuclear-neutrophils, 27-hydroxycholesterol fun

18 Polymorphonuclear neutrophil A3 receptors expression det

19 Myeloperoxidase, a heme enzyme released by polymorphonuclear neutrophils, accumulates within ischem

20 tic ketoacidosis is associated with systemic polymorphonuclear neutrophil activation and degranulatio

21 ted in partial inhibition of IL-8-stimulated polymorphonuclear neutrophil adhesion, and treatment wit

22 Polymorphonuclear neutrophils also express A3 adenosine

23 2-triggered neutrophilia and monocytosis and polymorphonuclear neutrophil and monocyte renal infiltra

24 cluded albumin leak into lung and buildup of polymorphonuclear neutrophils and cytokines/chemokines i

25 2B2 cells were compared with those of bovine polymorphonuclear neutrophils and lymphocytes.

26 With human polymorphonuclear neutrophils and macrophages, RvD1, RvD

27 icates the inflammatory response mediated by polymorphonuclear neutrophils and monocytes as the key e

28 which are cationic antimicrobial peptides of polymorphonuclear neutrophils and other leukocytes, are

29 hlamydia-specific immunoglobulin G (IgG) and polymorphonuclear neutrophils and show the importance of

30 00 magnification to quantitate the number of polymorphonuclear neutrophils and squamous epithelial ce

31 that this oxysterol increases the number of polymorphonuclear-neutrophils and gammadelta-T cells at

32 tions of 27-hydroxycholesterol requires both polymorphonuclear-neutrophils and gammadelta-T cells, an

33 ing the migration of monocytes, neutrophils, polymorphonuclear neutrophils, and dendritic cells into

34 Ceramide levels increase in activated polymorphonuclear neutrophils, and here we show that end

35 cells, macrophages, inflammatory monocytes, polymorphonuclear neutrophils, and in the spleen and liv

36 since leukocyte depletion by irradiation or polymorphonuclear neutrophil anti-serum pre-treatment el

37 n by reducing side effects in patients whose polymorphonuclear neutrophils are activated before hyper

38 Taken together, these findings suggest that polymorphonuclear neutrophils are capable of producing I

39 significantly inhibited the accumulation of polymorphonuclear neutrophils at the site of injury, neu

40 Of all the polymorphonuclear neutrophil azurophilic enzymes examine

41 , possibly due to the release of destructive polymorphonuclear neutrophil azurophilic enzymes.

42 surface markers detected on macrophages and polymorphonuclear neutrophils between the two strains.

43 to perforation, increased bacterial load and polymorphonuclear neutrophils, but decreased IFN-gamma a

44 d Y. pestis' ability to counter lysozyme and polymorphonuclear neutrophils, but it did not affect the

45 perinodal adipose tissues and non-apoptotic polymorphonuclear neutrophils carrying engulfed zymosan

46 g the role of specific genes associated with polymorphonuclear neutrophil cells.

47 Polymorphonuclear neutrophils constitute the first line

48 We now show that activated human polymorphonuclear neutrophils convert NO2- into NO2Cl an

49 with development of atopy was an increase in polymorphonuclear neutrophil-dendritic cell hybrid cells

50 eninges, parenchyma, and choroid plexus were polymorphonuclear neutrophil dependent, since leukocyte

51 is a hallmark of vascular inflammation, with polymorphonuclear neutrophil-derived (PMN-derived) and m

52 These results implicate DPPI and polymorphonuclear neutrophil-derived serine proteases in

53 protease stored in the azurophil granules of polymorphonuclear neutrophils, digests microbes after ph

54 binding; binding to FcgammaRI; activation of polymorphonuclear neutrophils; effect on the Ab-combinin

55 the activity of neutrophil serine proteases polymorphonuclear (neutrophil) elastase, cathepsin G, an

56 In this study, we show that polymorphonuclear neutrophils from mice deficient in ser

57 ased N-NO-IQ formation was not detected with polymorphonuclear neutrophils from two unrelated MPO-def

58 express A3 adenosine receptors that enhance polymorphonuclear neutrophil functions.

59 Polymorphonuclear neutrophil granulocytes (neutrophils)

60 nds on phagocytosis of invading pathogens by polymorphonuclear neutrophil granulocytes (PMNs), follow

61 translates into increased transmigration of polymorphonuclear neutrophil granulocytes across endothe

62 demonstrated an attenuated extravasation of polymorphonuclear neutrophil granulocytes in Sema7a-defi

63 r knowledge, of how Leishmania-induced human polymorphonuclear neutrophil (hPMN) autophagy regulates

64 also relieved cys-SPMs' actions in limiting polymorphonuclear neutrophil in E. coli exudates.

65 l/6 mice; P<.05) and decreased percentage of polymorphonuclear neutrophils in bronchoalveolar lavage

66 timulated EC also bound increased numbers of polymorphonuclear neutrophils in cellular adhesion assay

67 increasing macrophage ingestion of apoptotic polymorphonuclear neutrophils in vivo and in vitro, and

68 y binds to circulating and sequestered human polymorphonuclear neutrophils in vivo, eliminating in vi

69 and possibly inflammatory monocytes, but not polymorphonuclear neutrophils, in clearing HSV-1 from th

70 Sequestration of polymorphonuclear neutrophils (increased myeloperoxidase

71 saline resuscitation inhibits or aggravates polymorphonuclear neutrophil-induced acute lung injury.

72 7 and induced superoxide anion production by polymorphonuclear neutrophils; induction of the oxidativ

73 ilencing also increased bacterial counts and polymorphonuclear neutrophil infiltration in BALB/c corn

74 n of TNF-alpha and IL-1beta and interstitial polymorphonuclear neutrophil infiltration in vitro and i

75 ion, resulting in a prolonged stimulation of polymorphonuclear neutrophil influx into cornea.

76 racterized by microvascular permeability and polymorphonuclear neutrophil influx.

77 ation, there was a predominant infiltrate of polymorphonuclear neutrophils into the bladder.

78 Infiltration of polymorphonuclear neutrophils into the lung is an import

79 rain barrier permeability and recruitment of polymorphonuclear neutrophils into the tissue around the

80 (INT) reductase activity of disrupted bovine polymorphonuclear neutrophils is closely associated with

81 INT diaphorase activity of disrupted bovine polymorphonuclear neutrophils is shown to be resolved by

82 We further found that polymorphonuclear neutrophils isolated from normal donor

83 mRNA from human polymorphonuclear neutrophil leucocytes (PMNs) was probe

84 of Blood, Sapey et al. report that the human polymorphonuclear neutrophil leukocyte (or neutrophil) u

85 In polymorphonuclear neutrophils, leukocyte-specific protei

86 er, initiating steps leading to tethering of polymorphonuclear neutrophil leukocytes to the vascular

87 igration process of host inflammatory cells (polymorphonuclear neutrophils, macrophages) into the inf

88 We have shown that polymorphonuclear neutrophils mediate the covalent cross

89 Polymorphonuclear neutrophil-mediated inactivation of en

90 Polymorphonuclear neutrophil-mediated nitration and chlo

91 phenolic substrates, confirming its role in polymorphonuclear neutrophil-mediated nitration reaction

92 Polymorphonuclear neutrophils, monocytes, and macrophage

93 utrophils, tumor-associated neutrophils, and polymorphonuclear neutrophil myeloid-derived suppressor

94 Endothelial cell injury by polymorphonuclear neutrophil (neutrophil [PMN]) respirat

95 ce was accompanied by a reduction in corneal polymorphonuclear neutrophil number, bacterial load, and

96 ed as the 47-kD protein overexpressed in the polymorphonuclear neutrophils of patients with a rare ne

97 intracellular IFN-gamma was identified as a polymorphonuclear neutrophil on the basis of its reactiv

98 0.023), serum CRP level (P < 0.001) and oral polymorphonuclear neutrophil (oPMN) count (P < 0.001) wa

99 Oral polymorphonuclear neutrophil (oPMN) levels are potential

100 h reactive oxygen species production by oral polymorphonuclear neutrophils (oPMNs) in chronic periodo

101 groups based on the absolute counts of oral polymorphonuclear neutrophils (oPMNs).

102 GFR, fibroblast growth factor receptor; PMN, polymorphonuclear neutrophil; PDGF, platelet-derived gro

103 ed as visible urethral discharge and/or >/=5 polymorphonuclear neutrophils per high-powered field; n

104 inflammation after surgery, with the median polymorphonuclear neutrophil percentage decreasing from

105 hermore, these studies strongly suggest that polymorphonuclear neutrophils play an important role in

106 y agents yet their mechanism(s) for blocking polymorphonuclear neutrophil (PMN) accumulation at sites

107 perated calcium entry (SOCE) is required for polymorphonuclear neutrophil (PMN) activation in respons

108 Polymorphonuclear neutrophil (PMN) activation is pivotal

109 adenosine triphosphate (ATP) contributes to polymorphonuclear neutrophil (PMN) activation leading to

110 iphosphate (ATP) and adenosine in regulating polymorphonuclear neutrophil (PMN) activation, fibrin fo

111 lly relevant concentrations of ONOO- inhibit polymorphonuclear neutrophil (PMN) adhesion to the endot

112 rochetes, TNF-like and IL-1-like activities, polymorphonuclear neutrophil (PMN) chemotaxis-inducing a

113 re strongly related to BAL total protein and polymorphonuclear neutrophil (PMN) concentration, wherea

114 ied by a delay in the rise of the peripheral polymorphonuclear neutrophil (PMN) count and a paucity o

115 lear factor kappa-Beta ligand [RANKL]), oral polymorphonuclear neutrophil (PMN) counts, and systemic

116 -onset periodontal disease associated with a polymorphonuclear neutrophil (PMN) defective migratory r

117 Several types of polymorphonuclear neutrophil (PMN) deficiency are a pred

118 Myeloperoxidase (MPO) is released during polymorphonuclear neutrophil (PMN) degranulation, and me

119 coconjugated ligands are essential for blood polymorphonuclear neutrophil (PMN) extravasation into in

120 Polymorphonuclear neutrophil (PMN) extravasation require

121 formed to determine aging-related changes in polymorphonuclear neutrophil (PMN) function after cornea

122 ine receptors CXCR1 and CXCR2 are central to polymorphonuclear neutrophil (PMN) function.

123 To determine whether platelet and polymorphonuclear neutrophil (PMN) functions require spe

124 to facilitate immune complex (IC)-stimulated polymorphonuclear neutrophil (PMN) functions.

125 metabolite, adenosine, are key regulators of polymorphonuclear neutrophil (PMN) functions.

126 nt, a myeloperoxidase (MPO) assay to measure polymorphonuclear neutrophil (PMN) infiltrate, real-time

127 cin treatment also increased clinical score, polymorphonuclear neutrophil (PMN) infiltration (determi

128 Early preclinical events include polymorphonuclear neutrophil (PMN) infiltration and neov

129 heral organs in the two groups, WNV-infected polymorphonuclear neutrophil (PMN) infiltration and vira

130 onfirmed with synthetic MaR1, i.e., limiting polymorphonuclear neutrophil (PMN) infiltration in murin

131 reduced level of mast cell degranulation and polymorphonuclear neutrophil (PMN) infiltration in the s

132 del of this prevalent human disease, a heavy polymorphonuclear neutrophil (PMN) infiltration of the i

133 mBD2 and mBD3 that modulate bacterial load, polymorphonuclear neutrophil (PMN) infiltration, and pro

134 r to clinical observations, a robust vaginal polymorphonuclear neutrophil (PMN) migration occurs in a

135 observations revealed that a robust vaginal polymorphonuclear neutrophil (PMN) migration occurs in s

136 in response to C. albicans, which stimulate polymorphonuclear neutrophil (PMN) migration to the vagi

137 Treatment with rVIP decreased NO levels and polymorphonuclear neutrophil (PMN) number.

138 In addition to stimulating polymorphonuclear neutrophil (PMN) production, G-CSF may

139 lamp, histopathology, bacterial counts, and polymorphonuclear neutrophil (PMN) quantitation were per

140 eta-cyclodextrin to deplete cholesterol from polymorphonuclear neutrophil (PMN) rafts and thus study

141 of the junctional epithelium (P < 0.01) and polymorphonuclear neutrophil (PMN) recruitment (P < 0.00

142 arly coordinate appearance of LT and PG with polymorphonuclear neutrophil (PMN) recruitment.

143 Human polymorphonuclear neutrophil (PMN) responses to G protei

144 ours by high lethality, vascular congestion, polymorphonuclear neutrophil (PMN) sequestration in the

145 -surface protein, plays an important role in polymorphonuclear neutrophil (PMN) transmigration across

146 CAP37 is a polymorphonuclear neutrophil (PMN)-derived inflammatory

147 and G-CSF, alone or in combination, requires polymorphonuclear neutrophil (PMN)-derived proteases.

148 nally considered the fundamental trigger for polymorphonuclear neutrophil (PMN)-mediated damage.

149 ), an oligomeric enzyme, plays a key role in polymorphonuclear neutrophil (PMN)-mediated host defense

150 ne-enhancing properties that influence human polymorphonuclear neutrophil (PMN)-mediated mold hyphal

151 Pulmonary tuberculosis (TB) can present with polymorphonuclear neutrophil (PMN)-predominant alveoliti

152 1 is released in large amounts from adherent polymorphonuclear neutrophils (PMN) and binds to their c

153 activate integrin-mediated adhesion in human polymorphonuclear neutrophils (PMN) and monocytes cause

154 Polymorphonuclear neutrophils (PMN) are an important com

155 ogether with the previous demonstration that polymorphonuclear neutrophils (PMN) are critical for the

156 Polymorphonuclear neutrophils (PMN) are critical innate

157 Here we show that plastin-deficient polymorphonuclear neutrophils (PMN) are deficient in kil

158 /80(-)I-A(-) intraglomerular macrophages and polymorphonuclear neutrophils (PMN) are important in ind

159 Polymorphonuclear neutrophils (PMN) are linked invariabl

160 Polymorphonuclear neutrophils (PMN) are phagocytic cells

161 Polymorphonuclear neutrophils (PMN) are potent inflammat

162 Circulating polymorphonuclear neutrophils (PMN) are quiescent, nonad

163 Human polymorphonuclear neutrophils (PMN) chemotax to a foreig

164 Polymorphonuclear neutrophils (PMN) contain multiple dis

165 ated whether survival of the pathogen inside polymorphonuclear neutrophils (PMN) contributes to the p

166 We find that human polymorphonuclear neutrophils (PMN) equilibrated with a

167 Fc domain of IgG (Fc gamma R), only primate polymorphonuclear neutrophils (PMN) express an Fc gamma

168 Polymorphonuclear neutrophils (PMN) facilitate melanoma

169 s, the biologic forms and function of PR3 in polymorphonuclear neutrophils (PMN) from healthy donors

170 Polymorphonuclear neutrophils (PMN) have distinct phenot

171 The role of polymorphonuclear neutrophils (PMN) in mediating diabeti

172 Polymorphonuclear neutrophils (PMN) in Pseudomonas aerug

173 The primary function of polymorphonuclear neutrophils (PMN) in the immune respon

174 smic antibodies (ANCA) activate primed human polymorphonuclear neutrophils (PMN) in vitro, resulting

175 se-derived eicosanoids on apoptosis of human polymorphonuclear neutrophils (PMN) in vitro.

176 Adherence or recruitment of polymorphonuclear neutrophils (PMN) induces nuclear impo

177 IL-33) and disease severity, bacterial load, polymorphonuclear neutrophils (PMN) infiltrate, gene exp

178 Notably, not only MoPh but also polymorphonuclear neutrophils (PMN) ingested Clo-Lip in

179 Because polymorphonuclear neutrophils (PMN) interaction with ECs

180 l antibody was used to block infiltration of polymorphonuclear neutrophils (PMN) into the cornea.

181 Polymorphonuclear neutrophils (PMN) kill Cryptococcus ne

182 this study, we explored a novel function of polymorphonuclear neutrophils (PMN) NAD(P)H oxidase in t

183 In this study, the role of polymorphonuclear neutrophils (PMN) on the development o

184 Polymorphonuclear neutrophils (PMN) play a central role

185 of this study was to determine whether local polymorphonuclear neutrophils (PMN) recruitment and comp

186 e of alphaMbeta2 affected the recruitment of polymorphonuclear neutrophils (PMN) to bacterial and fun

187 t-mediated phagocytosis and firm adhesion of polymorphonuclear neutrophils (PMN) under physiological

188 er PGE(2) could inhibit bacterial killing by polymorphonuclear neutrophils (PMN) using a mouse model

189 ired in patients with congenital neutrophil (polymorphonuclear neutrophils (PMN)) defects.

190 is expressed on human leukocytes, including polymorphonuclear neutrophils (PMN), monocytes, and macr

191 t metabolizes glutamine, is present in human polymorphonuclear neutrophils (PMN).

192 s associated with diminished infiltration of polymorphonuclear neutrophils (PMN).

193 ation by recognizing and ingesting apoptotic polymorphonuclear neutrophils (PMN).

194 tion of alpha(M)beta(2)-mediated adhesion in polymorphonuclear neutrophils (PMN).

195 iated with significant tumor infiltration by polymorphonuclear neutrophils (PMN).

196 ) aggregation and deformability, neutrophil (polymorphonuclear neutrophil; PMN) deformability, whole-

197 Neutrophils (polymorphonuclear neutrophils; PMN) and a redundant syst

198 Polymorphonuclear neutrophil (PMNL) activation enhances

199 influenza virus is commonly associated with polymorphonuclear neutrophil (PMNL) dysfunction and cons

200 Migration of polymorphonuclear neutrophils (PMNL) from the vascular c

201 ein to the surfaces of infected cells, human polymorphonuclear neutrophils (PMNL) loaded with azithro

202 tly expressed on pulmonary epithelium and on polymorphonuclear neutrophil (PMNs) after transepithelia

203 on correlates with a vaginal infiltration of polymorphonuclear neutrophils (PMNs) and a high vaginal

204 how that stimulation of alpha7nAChR on human polymorphonuclear neutrophils (PMNs) and blood mononucle

205 its ligand, CXCL12, mediate the retention of polymorphonuclear neutrophils (PMNs) and hematopoietic s

206 e time, the expression of CD18 and ICAM-1 on polymorphonuclear neutrophils (PMNs) and hepatic cells w

207 vitro model of transepithelial migration of polymorphonuclear neutrophils (PMNs) and in human intest

208 TUNEL staining, real-time RT-PCR, polymorphonuclear neutrophils (PMNs) and macrophage (Mph

209 mice with ALI had greater increases in lung polymorphonuclear neutrophils (PMNs) and macrophage coun

210 Polymorphonuclear neutrophils (PMNs) and macrophages are

211 Polymorphonuclear neutrophils (PMNs) and NK cells are bo

212 Neutrophils or polymorphonuclear neutrophils (PMNs) are an important co

213 Polymorphonuclear neutrophils (PMNs) are critical for th

214 Polymorphonuclear neutrophils (PMNs) are essential effec

215 Polymorphonuclear neutrophils (PMNs) are increasingly re

216 Polymorphonuclear neutrophils (PMNs) are innate effector

217 Polymorphonuclear neutrophils (PMNs) are innate immune s

218 Polymorphonuclear neutrophils (PMNs) are largely conside

219 Polymorphonuclear neutrophils (PMNs) are quantified to m

220 During pneumonia, polymorphonuclear neutrophils (PMNs) are recruited by ch

221 this infection METHODS: To determine whether polymorphonuclear neutrophils (PMNs) are required for di

222 Polymorphonuclear neutrophils (PMNs) become stuck on the

223 ET formation in vivo and the infiltration of polymorphonuclear neutrophils (PMNs) but also reduces fi

224 Notably, polymorphonuclear neutrophils (PMNs) can capture circula

225 Human polymorphonuclear neutrophils (PMNs) counteracted the pr

226 its functional relevance for recruitment of polymorphonuclear neutrophils (PMNs) during acute inflam

227 Trafficking of polymorphonuclear neutrophils (PMNs) during inflammation

228 ell infiltration with an increased number of polymorphonuclear neutrophils (PMNs) during the early st

229 ed X-ray fluorescence (SR-XRF), on vitrified polymorphonuclear neutrophils (PMNs) during the occurren

230 Polymorphonuclear neutrophils (PMNs) express a number of

231 Polymorphonuclear neutrophils (PMNs) figure prominently

232 Polymorphonuclear neutrophils (PMNs) form the first line

233 We observed that polymorphonuclear neutrophils (PMNs) from FcgammaRIIIB w

234 nfection in skin involves the recruitment of polymorphonuclear neutrophils (PMNs) from the bone marro

235 Polymorphonuclear neutrophils (PMNs) from these KO mice

236 Polymorphonuclear neutrophils (PMNs) have previously bee

237 lysis, we characterized the heterogeneity of polymorphonuclear neutrophils (PMNs) in cancer.

238 fection, Tlr5(-/-) mice had lower numbers of polymorphonuclear neutrophils (PMNs) in their broncho-al

239 fect of anti-LcrV antibody extended to mouse polymorphonuclear neutrophils (PMNs) in vitro, and PMNs

240 Numerous studies have shown that polymorphonuclear neutrophils (PMNs) infiltrate the myoc

241 Polymorphonuclear neutrophils (PMNs) infiltrate tissue i

242 onse to chemoattractant stimulation in human polymorphonuclear neutrophils (PMNs) is characterized by

243 uces pro-inflammatory cytokine production by polymorphonuclear neutrophils (PMNs) of diabetic individ

244 DGKalpha function is altered in polymorphonuclear neutrophils (PMNs) of patients with lo

245 Polymorphonuclear neutrophils (PMNs) play a critical rol

246 During inflammation, circulating polymorphonuclear neutrophils (PMNs) receive signals to

247 unexpected activity of a CD49d(+) subset of polymorphonuclear neutrophils (PMNs) that are found in t

248 Bone marrow (BM) holds a large reserve of polymorphonuclear neutrophils (PMNs) that are rapidly mo

249 satetraenoate (5-HETE and 5-oxoETE) activate polymorphonuclear neutrophils (PMNs) through a common, r

250 These activate human polymorphonuclear neutrophils (PMNs) through formyl pept

251 re involved in recruitment and activation of polymorphonuclear neutrophils (PMNs) to infected tissues

252 Recruitment of polymorphonuclear neutrophils (PMNs) to sites of acute i

253 ammatory cytokines followed by attraction of polymorphonuclear neutrophils (PMNs) to the site of infl

254 During inflammation polymorphonuclear neutrophils (PMNs) traverse venular wa

255 Polymorphonuclear neutrophils (PMNs) treated with a subl

256 Activation of circulating polymorphonuclear neutrophils (PMNs) was assessed by an

257 CAF2-1, SSK21, and SSK23 to killing by human polymorphonuclear neutrophils (PMNs) was assessed.

258 unt, real-time RT-PCR, and ELISA assays, and polymorphonuclear neutrophils (PMNs) were quantitated us

259 Eighty-six genes in WG PBMCs and 40 in WG polymorphonuclear neutrophils (PMNs) were significantly

260 Interactions of polymorphonuclear neutrophils (PMNs) with endothelial ce

261 count for this absence, we hypothesized that polymorphonuclear neutrophils (PMNs), recruited massivel

262 Polymorphonuclear neutrophils (PMNs), the primary leukoc

263 ical, and gene manipulation methods in human polymorphonuclear neutrophils (PMNs), we have identified

264 edema formation induced by the activation of polymorphonuclear neutrophils (PMNs).

265 er nonself particles, specifically apoptotic polymorphonuclear neutrophils (PMNs).

266 ke phenotype to a small population of mature polymorphonuclear neutrophils (PMNs).

267 ADAM9 is also a product of human and murine polymorphonuclear neutrophils (PMNs).

268 ogous to CD16A and a major FcgammaR on human polymorphonuclear neutrophils (PMNs).

269 ion that is characterized by infiltration of polymorphonuclear neutrophils (PMNs; refs 1-4).

270 Tumor-infiltrating neutrophils (polymorphonuclear neutrophils [PMNs]) are a prominent fe

271 is a risk factor for TRALI and neutrophils (polymorphonuclear neutrophils [PMNs]) are considered to

272 Neutrophils (polymorphonuclear neutrophils [PMNs]) play an elaborate

273 Blood polymorphonuclear neutrophils provide immune protection

274 Polymorphonuclear neutrophils recruited to the infected

275 endothelial cells that appear essential for polymorphonuclear neutrophil recruitment in IC disease.

276 cant differences in bacterial numbers and in polymorphonuclear neutrophil recruitment in the lungs fr

277 rease in blood-brain barrier permeability or polymorphonuclear neutrophil recruitment, but did give r

278 Polymorphonuclear neutrophils release ATP in response to

279 er, histological analyses suggested that the polymorphonuclear neutrophil response at 2 days postinfe

280 In studies of human polymorphonuclear neutrophil responses to formyl peptide

281 To test individual mosaic subpopulations of polymorphonuclear neutrophil responses, we also develope

282 whereas adoptive transfer of MD-2-competent polymorphonuclear neutrophils restored it.

283 e that is converted to adenosine, inhibiting polymorphonuclear neutrophils through A2a adenosine rece

284 ggregation initiates activation signaling in polymorphonuclear neutrophils through at least two disti

285 te inflammation by blocking the migration of polymorphonuclear neutrophils to initiate resolution.

286 rane response increased the ability of human polymorphonuclear neutrophils to readily clear both E. f

287 Hypertonic saline triggers polymorphonuclear neutrophils to release adenosine triph

288 the adhesion of a type of white blood cell--polymorphonuclear neutrophils--to the lining of the circ

289 Interestingly, C5a-stimulated endothelial polymorphonuclear neutrophil transmigration, but not che

290 cally upregulated by the action of activated polymorphonuclear neutrophils via an unprecedented mecha

291 Elevated counts of polymorphonuclear neutrophils were detectable at 15 minu

292 eripheral blood mononuclear cells (PBMC) and polymorphonuclear neutrophils were induced to express DD

293 Polymorphonuclear neutrophils were stimulated with buffe

294 Treatment of human polymorphonuclear neutrophils with hypertonic saline bef

295 reased cellular ceramide content by treating polymorphonuclear neutrophils with sphingomyelinase C an