ライフサイエンスコーパス: leukocyte recruitment

1 -associated antigen 1 (LFA-1) activation and leukocyte recruitment.

2 ranscript levels of M1 cytokines involved in leukocyte recruitment.

3 ies for disorders characterized by excessive leukocyte recruitment.

4 GEFs play important proinflammatory roles in leukocyte recruitment.

5 2) or P2X(1), antagonism inhibited pulmonary leukocyte recruitment.

6 arly genes involved in cellular movement and leukocyte recruitment.

7 harbors a novel approach to target arterial leukocyte recruitment.

8 in regulating microvascular permeability and leukocyte recruitment.

9 o neutrophils, an important event in driving leukocyte recruitment.

10 enesis of inflammatory diseases by promoting leukocyte recruitment.

11 , and plasminogen plays an important role in leukocyte recruitment.

12 ess so, and CCR5 plays only a modest role in leukocyte recruitment.

13 f venules specialized for plasma leakage and leukocyte recruitment.

14 Integrins are recognized as vital players in leukocyte recruitment.

15 and modulating corticosterone production and leukocyte recruitment.

16 ncy in PSGL-1 and ESL-1 completely abrogated leukocyte recruitment.

17 vasins, which bind to chemokines and prevent leukocyte recruitment.

18 y with the potential to inhibit inflammatory leukocyte recruitment.

19 ducing inflammatory diseases associated with leukocyte recruitment.

20 pathways leading to integrin activation and leukocyte recruitment.

21 xchanging factor, in integrin activation and leukocyte recruitment.

22 apable of homing to the prostate and induced leukocyte recruitment.

23 t hematopoietic ppGalNAcT-1 is important for leukocyte recruitment.

24 ucing proinflammatory cytokine synthesis and leukocyte recruitment.

25 oprotein ligand-1 plays an important role in leukocyte recruitment.

26 n of inflammation failed, leading to chronic leukocyte recruitment.

27 osphate (cGMP)-signaling, leading to reduced leukocyte recruitment.

28 ion receptor E-selectin and in microvascular leukocyte recruitment.

29 lood vessels and contributes to inflammatory leukocyte recruitment.

30 ct suppression of endothelial activation and leukocyte recruitment.

31 ot explained by enhanced immunity or reduced leukocyte recruitment.

32 alyzed the effects of the RacGAP ArhGAP15 on leukocyte recruitment.

33 ction exacerbates endothelial exocytosis and leukocyte recruitment.

34 tes and endothelial cells, thereby mediating leukocyte recruitment.

35 , and VCAM-1 and ultimately through enhanced leukocyte recruitment.

36 enes, including Ccl2 and Lcn2, implicated in leukocyte recruitment.

37 display full adult-type inflammation-induced leukocyte recruitment.(1) They report that murine fetal

38 iciency led to a reduction in: 1) total lung leukocyte recruitment; 2) Th2 and Th17 responses; 3) tot

39 abbit arteries, cell proliferation (51%) and leukocyte recruitment (41%) were reduced at 3 d, and neo

40 ific overexpression of DEL-1 linked its anti-leukocyte-recruitment action to endothelial cell-derived

41 endogenous Duox1 activity, H2O2 release and leukocyte recruitment after tissue injury, with none of

42 ation by reducing endothelial activation and leukocyte recruitment along with limiting proinflammator

43 CXCR1 and CXCR2 couple to Galphai to induce leukocyte recruitment and activation at sites of inflamm

44 CXCR1 and CXCR2, couple to Galphai to induce leukocyte recruitment and activation at sites of inflamm

45 We show that leukocyte recruitment and activation can be separated.

46 oliferation of liver cells and on regulating leukocyte recruitment and activation in liver IRI.

47 Spleen tyrosine kinase (Syk) promotes leukocyte recruitment and activation via signaling throu

48 Indeed, the protective effect of IVIG on leukocyte recruitment and activation was abrogated in SH

49 Leukocyte recruitment and activation within the lungs we

50 ral mechanisms that include an inhibition of leukocyte recruitment and activation.

51 ion of proinflammatory molecules involved in leukocyte recruitment and adherence to endothelium, incl

52 CR1) comprise a chemokine system involved in leukocyte recruitment and adhesion in atherosclerosis, b

53 and its potential contribution to modulating leukocyte recruitment and alleviating different inflamma

54 Chemokines are required for leukocyte recruitment and appropriate host defense and a

55 ctin and ICAM-1 expression are essential for leukocyte recruitment and are good markers of EC activat

56 as a promising target to reduce inflammatory leukocyte recruitment and arrest.

57 ted infection-induced hypothermia, augmented leukocyte recruitment and bacterial clearance, and decre

58 Leukocyte recruitment and C1q-hemolytic activity was res

59 time-lapse intravital microscopy to examine leukocyte recruitment and chemotaxis in vivo.

60 Targeting both VWF-mediated leukocyte recruitment and chromatin removal may be a new

61 or human recombinant RNase1 interfered with leukocyte recruitment and collateral artery growth.

62 ll-associated CD93, and not sCD93, regulates leukocyte recruitment and complement activation during m

63 ence tomography (OCT) were used to visualize leukocyte recruitment and corneal thickening.

64 lack of Tnc expression resulted in impaired leukocyte recruitment and decreased expressions of inter

65 sed wet-to-dry ratio, reduced neutrophil and leukocyte recruitment and decreased inflammatory cytokin

66 e results were associated with inhibition of leukocyte recruitment and decreased production of cytoki

67 a specific p90RSK inhibitor, ameliorated EC-leukocyte recruitment and diminished vascular reactivity

68 the brain but markedly reduces inflammatory leukocyte recruitment and enhances survival in a murine

69 ession through different pathways, including leukocyte recruitment and function, cellular senescence,

70 to atherosclerosis: inflammation, immunity, leukocyte recruitment and function, function of vascular

71 ascade of immunopathologic events, including leukocyte recruitment and granuloma formation.

72 Leukocyte recruitment and heterocellular aggregate forma

73 , abrogated the inhibitory effect of IVIG on leukocyte recruitment and heterotypic red blood cell (RB

74 ization during CKD in murine models restored leukocyte recruitment and host defense.

75 cytokines, several of which are involved in leukocyte recruitment and hypothesized to enhance suscep

76 for studying cardiac-specific mechanisms of leukocyte recruitment and identifying novel therapeutic

77 rin treatment significantly reduced cerebral leukocyte recruitment and increased endogenous levels of

78 and relayed to vascular responses, including leukocyte recruitment and increased endothelial permeabi

79 Our data indicate that IL-13 regulates leukocyte recruitment and induces M2-like monocyte/macro

80 Thrombin is a central regulator of leukocyte recruitment and inflammation at sites of vascu

81 mice in the footpad with papain and studied leukocyte recruitment and inflammatory cytokine and chem

82 CS-1 peptides significantly inhibited leukocyte recruitment and local release of proinflammato

83 lium, epithelium, and stromal cells controls leukocyte recruitment and microenvironmental localizatio

84 Leukocyte recruitment and migration induced by platelet

85 g, from the evolution of multistep models of leukocyte recruitment and navigation to the regulation o

86 This protection is associated with reduced leukocyte recruitment and NET formation at the site of t

87 Therefore, BI-mediated reduction in leukocyte recruitment and NETosis in the lungs are attri

88 trast, BI significantly reduced LPS-mediated leukocyte recruitment and NETosis.

89 t IL-1alpha acts as an alarmin essential for leukocyte recruitment and protective immunity against HS

90 yndrome in humans, characterized by impaired leukocyte recruitment and recurrent infections.

91 yndrome in humans, characterized by impaired leukocyte recruitment and recurrent infections.

92 e damage, the endothelial HA matrix enhances leukocyte recruitment and regulates the early stages of

93 sitive feedback mechanism involving enhanced leukocyte recruitment and release of pro-inflammatory cy

94 ete proinflammatory cytokines, which trigger leukocyte recruitment and renal inflammation.

95 Pulmonary leukocyte recruitment and splenic or pulmonary T cell cy

96 d contribute to DVT progression by promoting leukocyte recruitment and stimulating neutrophil-depende

97 nsforming growth factor-beta , which limited leukocyte recruitment and survival, and produced high le

98 /3 in mast cells decreased the IL-33-induced leukocyte recruitment and the resulting skin inflammatio

99 tes both key events in sterile inflammation, leukocyte recruitment and their induction to secrete inf

100 lature and defines subset specialization for leukocyte recruitment and vascular homeostasis.

101 In vivo, we found increased leukocyte recruitment and vascular permeability/inflamma

102 bacterial burden and was accompanied by less leukocytes recruitment and attenuated inflammatory respo

103 regulation of membrane protein trafficking, leukocyte recruitment, and adhesion processes.

104 pates in MC activation, protease maturation, leukocyte recruitment, and angiogenesis-all processes cr

105 mine T-lymphocyte polarization, inflammatory leukocyte recruitment, and biliary injury in rhesus rota

106 ested by parenchymal gadolinium enhancement, leukocyte recruitment, and endothelial activation.

107 reases in cytokine and chemokine expression, leukocyte recruitment, and hepatic inflammation.

108 lation, hepatic transcripts level related to leukocyte recruitment, and hepatic RNA-seq analysis.

109 CrmD dampened pathology, leukocyte recruitment, and inflammatory cytokine product

110 duced without impairing cytokine production, leukocyte recruitment, and pathogen clearance.

111 terial clearance, proinflammatory mediators, leukocyte recruitment, and phagocyte activities were mea

112 ng CXCR3 in leukocytes significantly reduced leukocyte recruitment, and prevented RGC death at 7 days

113 welling, SK activity, vascular permeability, leukocyte recruitment, and production of proinflammatory

114 irway inflammation using immunofluorescence, leukocyte recruitment, and quantitative RT-PCR.

115 s in the lungs and CNS, diminished pulmonary leukocyte recruitment, and simultaneously impaired Th1 a

116 tivation, thrombin generation, platelet, and leukocyte recruitment, and the initiation of innate and

117 ycin-treated mice presented with an enhanced leukocyte recruitment as assessed by (18)F-FBEM-labeled

118 of the key approaches used for understanding leukocyte recruitment as it occurs throughout the body,

119 and counteract integrin activation and limit leukocyte recruitment at the site of inflammation.

120 -induced protein 10, which are implicated in leukocyte recruitment but also in protection from lung i

121 TNF deficiency did not affect viral load or leukocyte recruitment but caused severe lung pathology a

122 IAV-infected mice revealed markedly enhanced leukocyte recruitment but impaired production of type I

123 BoxA, a HMGB1 inhibitor, interferes with leukocyte recruitment but not with activation.

124 bition of HIV infection, cell migration, and leukocyte recruitment but, importantly, not the mobiliza

125 regulates Mac-1, but not LFA-1, and affects leukocyte recruitment by controlling postadhesion streng

126 ated that extracellular RNA (eRNA) regulated leukocyte recruitment by engaging vascular endothelial g

127 ic acid) in reducing ex vivo human SCD blood leukocyte recruitment by microvascular endothelial cells

128 m conservation of the receptor signaling and leukocyte recruitment capacities of human MIF by its pla

129 8/14 and TLR4 as important modulators of the leukocyte recruitment cascade during inflammation in viv

130 stablished to examine different steps of the leukocyte recruitment cascade in vivo and in vitro under

131 These results refine the leukocyte recruitment cascade model by introducing endot

132 we demonstrated that different steps of the leukocyte recruitment cascade were affected in CD45E613R

133 in activation for the different steps of the leukocyte recruitment cascade, including rolling, adhesi

134 maRIII mediated IVIG-triggered inhibition of leukocyte recruitment, circulating RBC capture, and enha

135 Leukocyte recruitment, cytokine production, and bacteria

136 Leukocyte recruitment, cytokine production, and bacteria

137 d airway inflammation, we observed decreased leukocyte recruitment, cytokine production, and mucin pr

138 Though the overall phenotype resembled the leukocyte recruitment defect observed in beta2 integrin-

139 st to seek novel compounds that can regulate leukocyte recruitment depending on the degree of inflamm

140 Leukocyte recruitment did not occur without coitus or wi

141 exogenous and endogenous Gal-3 in promoting leukocyte recruitment during acute inflammation.

142 ncy caused arterial leakage and inflammatory leukocyte recruitment during atherogenesis.

143 The proteoglycan decorin modulates leukocyte recruitment during delayed-type hypersensitivi

144 GFP (neutrophil reporter) mice, investigated leukocyte recruitment during fetal development.

145 n successfully reduced viral replication and leukocyte recruitment during infection.

146 Leukocyte recruitment during inflammation must be tightl

147 g behavior on E-selectin, a critical step in leukocyte recruitment during inflammation.

148 R mutation modulates integrin activation and leukocyte recruitment during inflammation.

149 Chemokines promote leukocyte recruitment during inflammation.

150 ine postcapillary venules, a primary site of leukocyte recruitment during inflammation.

151 the orchestration of cytokine production and leukocyte recruitment during influenza virus infection,

152 sins regulate chemokine activity and thereby leukocyte recruitment during protective or pathological

153 less host cell apoptosis, decreased hepatic leukocyte recruitment, enhanced bacterial clearance, and

154 ut are primed to potentiate inflammation and leukocyte recruitment following ischemic injury.

155 ted signaling pathways are also critical for leukocyte recruitment following wounding in larval zebra

156 In adult mammals, leukocyte recruitment follows a well-defined cascade of

157 Cathepsin B-mediated CD18 shedding regulates leukocyte recruitment from angiogenic vessels.

158 During inflammation, leukocyte recruitment has to be tightly controlled to pr

159 t strain of C. neoformans through effects on leukocyte recruitment, IFN-gamma production by CD4 and C

160 enable monitoring of metabolic activity and leukocyte recruitment in a mouse model of pulmonary fibr

161 temic absence of this plasma protein affects leukocyte recruitment in alveolitis models of lung infla

162 WKYMVm-induced leukocyte recruitment in chimeric mice (WT bone marrow t

163 tis model, leveraging the natural pathway of leukocyte recruitment in inflammatory tissue.

164 that gain access to the prostate and induce leukocyte recruitment in mice with different susceptibil

165 leaving von Willebrand factor (VWF), reduces leukocyte recruitment in mice.

166 Leukocyte recruitment in response to inflammatory signal

167 These results indicate that leukocyte recruitment in retinal vessels near the ON hea

168 uced corticosterone generation, and impaired leukocyte recruitment in sepsis.

169 ed to investigate the effect of lidocaine on leukocyte recruitment in septic patients.

170 Leukocyte recruitment in the airways, cytokine levels, a

171 Therapeutic targeting of arterial leukocyte recruitment in the context of atherosclerosis

172 Here we examine chemokine expression and leukocyte recruitment in the context of avirulent and vi

173 , allegedly more selective drugs that affect leukocyte recruitment in the gastrointestinal tract have

174 tened histological signs of inflammation and leukocyte recruitment in the GBS-infected kidney.

175 lation, complement, platelet activation, and leukocyte recruitment in the microvasculature.

176 Leukocyte recruitment in thrombocytopenic mice remained

177 ukocyte recruitment in vivo, we investigated leukocyte recruitment in untreated and TNF-alpha-treated

178 duce acute VOC in SCD mice, characterized by leukocyte recruitment in venules, capture of circulating

179 l of insight into chemokine orchestration of leukocyte recruitment in viral encephalitis.

180 and stimulate cytokine secretion as well as leukocyte recruitment in vitro and in vivo.

181 We evaluated leukocyte recruitment in vivo by using real-time multich

182 kine receptors, dimerization is required for leukocyte recruitment in vivo, and it remains controvers

183 ein ligand-1 by ppGalNAcT-1 is important for leukocyte recruitment in vivo, we investigated leukocyte

184 to wild type MCP-1 in its ability to induce leukocyte recruitment in vivo, whereas the obligate dime

185 t MCP-1(T10C) was less effective at inducing leukocyte recruitment in vivo.

186 e data suggest a critical role of Adam10 for leukocyte recruitment, inflammatory mediator production,

187 nd fungal infections as a result of impaired leukocyte recruitment, ingestion, and/or killing of micr

188 proteins and antiproteases were reduced, and leukocyte recruitment (interleukin-8 pathway, P = 1.41E-

189 netics of cytokine and chemokine production, leukocyte recruitment, intestinal permeability, and T-ce

190 tle is known about the dynamic regulation of leukocyte recruitment into inflamed heart tissue, largel

191 Here, we have shown that CKD impairs leukocyte recruitment into inflamed tissue and host defe

192 tion in secondary lymphoid organs, real-time leukocyte recruitment into inflamed tissues is not well

193 h may be important for precise regulation of leukocyte recruitment into inflamed tissues.

194 dhesive properties of the endothelium and on leukocyte recruitment into obese adipose depots.

195 d inflammation was associated with decreased leukocyte recruitment into the colonic lamina propria.

196 ce attenuated EAE susceptibility by reducing leukocyte recruitment into the injury regions of the spi

197 Myeloid leukocyte recruitment into the lung in response to envir

198 ndent leukocyte slow rolling, which promotes leukocyte recruitment into tissues.

199 Leukocyte recruitment is a central immune process.

200 Chemokine-controlled arterial leukocyte recruitment is a crucial process in atheroscle

201 Leukocyte recruitment is a universal feature of tissue i

202 However, we identified that reduced leukocyte recruitment is accompanied by reduced vascular

203 Deciphering the molecular basis of leukocyte recruitment is critical to the understanding o

204 Leukocyte recruitment is generally achieved by rapid mig

205 ines are central to this process and whether leukocyte recruitment is important for limiting viral pr

206 echanotransduction events resulting in local leukocyte recruitment is not understood.

207 ndings demonstrate that inflammation-induced leukocyte recruitment is ontogenetically regulated and e

208 receptor (RXR)alpha on arterial mononuclear leukocyte recruitment is poorly understood, this study i

209 A central regulator of leukocyte recruitment is Rac1.

210 the role of protein tyrosine phosphatases in leukocyte recruitment is still elusive.

211 rmylated peptides to integrin activation and leukocyte recruitment is unknown.

212 es, but its involvement in the regulation of leukocyte recruitment is unknown.

213 haracterized by increasing polymorphonuclear leukocyte recruitment, is a major cause of the decline i

214 that although BMP9 alone does not influence leukocyte recruitment, it primes the vascular endotheliu

215 tational age in humans, we hypothesized that leukocyte recruitment may be acquired only late during f

216 Therapies targeting leukocyte recruitment may be beneficial in reducing vasc

217 propose that locally produced modulators of leukocyte recruitment may represent local homeostatic me

218 on of the MIF-CXCR2 and -CXCR4 axes promotes leukocyte recruitment, mediating the exacerbating role o

219 es of mice demonstrated that histones induce leukocyte recruitment, microvascular vascular leakage, r

220 nd enhanced proliferation without triggering leukocyte recruitment or overt neuropathology.

221 Lp(a)/apo(a) modifies plasminogen-dependent leukocyte recruitment or whether apo(a) has an independe

222 Variable effects on leukocyte recruitment, pathogenesis, and immunity were o

223 ve and Gram-positive infections via enhanced leukocyte recruitment, phagocytosis, and respiratory bur

224 ion and induction of mediators orchestrating leukocyte recruitment, possibly by reducing NF-kappaB ac

225 oding Galpha(i2)), consistent with a reduced leukocyte recruitment previously observed in Gnai2 (-/-)

226 Currently, it is unclear whether leukocyte recruitment proceeds in a similar fashion duri

227 ling in IL-1R1 null mice globally attenuated leukocyte recruitment, reducing the number of infiltrati

228 oxide (NO) plays a key role in the enhanced leukocyte recruitment reflective of systemic inflammatio

229 wever, cell-specific function of LSP1 during leukocyte recruitment remains elusive.

230 s performed to assess metabolic activity and leukocyte recruitment, respectively.

231 limited neointima formation with attenuated leukocyte recruitment, resulting from diminished inducti

232 peptidomimetic also exhibited reduced kidney leukocyte recruitment (T lymphocytes and classic M1 proi

233 usion), we demonstrate a distinct process of leukocyte recruitment, termed "directed intravascular mi

234 ural insights into how defensin orchestrates leukocyte recruitment through GAG binding and G protein-

235 observed in vivo are the result of increased leukocyte recruitment through increased CXCR1/2 signalin

236 nitiation of liver inflammation by promoting leukocyte recruitment through sinusoidal endothelium.

237 ans believe that it occurs inevitably during leukocyte recruitment to a site of infection.

238 of regenerative medicine, the mechanisms of leukocyte recruitment to and actions at sites of angioge

239 te inflammation revealed a 24-hour rhythm in leukocyte recruitment to arteries and veins of the mouse

240 animal model for innate immunity, to measure leukocyte recruitment to damaged livers.

241 nflammatory response (from myelopoiesis over leukocyte recruitment to efferocytosis and resolution of

242 ell spread by L. monocytogenes, 2) defective leukocyte recruitment to infection foci, and 3) producti

243 into microcapsules, which enhanced i) human leukocyte recruitment to inflamed endothelium and ii) hu

244 Leukocyte recruitment to inflammation sites progresses i

245 n and movement (migration) are important for leukocyte recruitment to inflammation sites.

246 under flow conditions in vitro and inhibited leukocyte recruitment to injured carotid arteries in viv

247 ocorticoid production in adrenal glands, the leukocyte recruitment to peritoneum or the bacterial cle

248 muscle cellMsx1/2 knockout mice had reduced leukocyte recruitment to remodeling collateral arteries.

249 RATIONALE: Leukocyte recruitment to sites of allergic inflammation

250 opy, we examined the molecular mechanisms of leukocyte recruitment to sites of focal hepatic necrosis

251 Leukocyte recruitment to sites of inflammation is critic

252 ider not only the role of these molecules in leukocyte recruitment to sites of inflammation, but also

253 vascular function that promote or facilitate leukocyte recruitment to sites of inflammation.

254 s in a number of organs, including enhancing leukocyte recruitment to sites of injury and infection.

255 inflammatory diseases and is responsible for leukocyte recruitment to sites of its expression.

256 thrombin cleavage of platelet PAR4 promotes leukocyte recruitment to sites of vascular injury.

257 wild-type bone marrow cells did not restore leukocyte recruitment to the air pouch, indicating a rol

258 urinergic receptor P2X(7) can enhance airway leukocyte recruitment to the airways, and P2X(7) knockou

259 choroid plexus, where initial CCL20-induced leukocyte recruitment to the brain occurs, are identifie

260 and histochemical staining revealed impaired leukocyte recruitment to the central cornea and earlier

261 acquisition and shedding of HIV via chronic leukocyte recruitment to the cervical mucosa.

262 nt for mediating sickness behavior and drove leukocyte recruitment to the CNS and impaired neurogenes

263 Growing evidence suggests that leukocyte recruitment to the CNS is also increased with

264 nal inflammation, characterized by decreased leukocyte recruitment to the colons and reduced immune c

265 asis, we define a chemokine axis involved in leukocyte recruitment to the encephalitic brain during S

266 n alphaMbeta2, or CD11b/CD18) is crucial for leukocyte recruitment to the endothelium, and Mac-1 enga

267 have suggested a role for BMP9 signaling in leukocyte recruitment to the endothelium, but the direct

268 CR9) activation by CCL25 plays a key role in leukocyte recruitment to the gut and represents a therap

269 hich immune cell-expressed beta2ARs regulate leukocyte recruitment to the heart following acute cardi

270 infarction (MI) elicits massive inflammatory leukocyte recruitment to the heart.

271 ndividually and the resulting suppression of leukocyte recruitment to the infected brain have no effe

272 of galectin-3 (Gal-3) during the process of leukocyte recruitment to the inflamed microcirculation.

273 rocess in various diseases, characterized by leukocyte recruitment to the inflammatory site.

274 arch has investigated both the mechanisms of leukocyte recruitment to the kidney and the actions of i

275 a membrane-bound amine oxidase that promotes leukocyte recruitment to the liver, and the soluble form

276 Leukocyte recruitment to the lung and AHR were assessed

277 icits characteristic cytokine production and leukocyte recruitment to the lung parenchyma.

278 Leukocyte recruitment to the lungs and expression of inf

279 inhibitor, BAY73-6691, significantly altered leukocyte recruitment to the microvasculature.

280 As in other respiratory infections, leukocyte recruitment to the respiratory system in peopl

281 of modulating innate immunity by stimulating leukocyte recruitment to the site of infection, and prod

282 depth analysis of the chemokines involved in leukocyte recruitment to the virally infected brain and

283 e Pez ortholog (PTPN21) exhibit a failure in leukocyte recruitment to wounds.

284 eased proinflammatory mediator responses and leukocyte recruitment upon M. bovis BCG challenge, and t

285 Angiogenesis, mural cell investment, leukocyte recruitment, vascular permeability, reactive g

286 naling, inflammation, tissue remodeling, and leukocyte recruitment via cleavage of their target prote

287 In Sdc-1(-/-) mice, early leukocyte recruitment via the choroid plexus is enhanced

288 d with increased inflammation by stimulating leukocyte recruitment via up-regulation of circulating p

289 This deficit in alveolar leukocyte recruitment was also observed in LysM-Adam10(-

290 Leukocyte recruitment was defective upon induction of pe

291 Corneal leukocyte recruitment was determined using flow cytometr

292 In this work, the effect of aging on CNS leukocyte recruitment was examined.

293 However, extensive inflammation and leukocyte recruitment were not observed in the bladder,

294 yte migration in vitro and failed to promote leukocyte recruitment when added to murine air pouches (

295 26 may be superior in inhibition of arterial leukocyte recruitment when compared with blocking indivi

296 stinct pattern of endothelial activation and leukocyte recruitment when compared with the Th1 cytokin

297 C57BL/6 mice induced similar alterations in leukocyte recruitment, whereas hemin-induced inflammatio

298 hat Arhgap25 deficiency affects all steps of leukocyte recruitment with a predominant enhancement of

299 and rapid systemic inflammation and vascular leukocyte recruitment within 15 minutes, accompanied by

300 BMP9 treatment also increased leukocyte recruitment within the pulmonary circulation i