ライフサイエンスコーパス: leukocyte recruitment

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

2 enesis of inflammatory diseases by promoting leukocyte recruitment.

3 ction exacerbates endothelial exocytosis and leukocyte recruitment.

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

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

6 f venules specialized for plasma leakage and leukocyte recruitment.

7 Integrins are recognized as vital players in leukocyte recruitment.

8 and modulating corticosterone production and leukocyte recruitment.

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

10 y with the potential to inhibit inflammatory leukocyte recruitment.

11 ducing inflammatory diseases associated with leukocyte recruitment.

12 pathways leading to integrin activation and leukocyte recruitment.

13 xchanging factor, in integrin activation and leukocyte recruitment.

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

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

16 ucing proinflammatory cytokine synthesis and leukocyte recruitment.

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

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

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

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

21 lood vessels and contributes to inflammatory leukocyte recruitment.

22 ct suppression of endothelial activation and leukocyte recruitment.

23 ated and P-selectin contributed much less to leukocyte recruitment.

24 p-regulated and P-selectin was essential for leukocyte recruitment.

25 KYNA could be an important early mediator of leukocyte recruitment.

26 egulation of endothelial cell signals during leukocyte recruitment.

27 lial cell types, which subsequently promotes leukocyte recruitment.

28 cal response to vascular injury by promoting leukocyte recruitment.

29 dothelial cell adhesion molecule involved in leukocyte recruitment.

30 olic Ca(2+), leading to P-selectin-dependent leukocyte recruitment.

31 tes and endothelial cells, thereby mediating leukocyte recruitment.

32 presented by ECs and for promoting unwanted leukocyte recruitment.

33 thelium, thereby initiating Ca(2+)-dependent leukocyte recruitment.

34 mine oxidase (SSAO) activity, is involved in leukocyte recruitment.

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

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

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

38 ranscript levels of M1 cytokines involved in leukocyte recruitment.

39 ies for disorders characterized by excessive leukocyte recruitment.

40 GEFs play important proinflammatory roles in leukocyte recruitment.

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

42 arly genes involved in cellular movement and leukocyte recruitment.

43 harbors a novel approach to target arterial leukocyte recruitment.

44 in regulating microvascular permeability and leukocyte recruitment.

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

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

47 ted 1) organ microbial burdens, 2) pulmonary leukocyte recruitment, 3) pulmonary and systemic cytokin

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

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

50 addition, thioglycollate-induced peritoneal leukocyte recruitment and accumulation were substantiall

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

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

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

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

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

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

57 Leukocyte recruitment and activation within the lungs we

58 nt role in vascular inflammation by inducing leukocyte recruitment and activation.

59 chemokines beyond their traditional role in leukocyte recruitment and activation.

60 tractant protein-1, plays a critical role in leukocyte recruitment and activation.

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

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

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

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

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

66 Leukocyte recruitment and C1q-hemolytic activity was res

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 Although TGF-beta can enhance leukocyte recruitment and IgA production, it inhibits bo

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

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

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

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

87 mRNA stability in the intricate processes of leukocyte recruitment and inflammatory activation within

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

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

90 tic cytokines that play an important role in leukocyte recruitment and may directly or indirectly mod

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

92 Leukocyte recruitment and migration induced by platelet

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

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

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

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

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

98 In contrast, IL-2/anti-CD40-mediated leukocyte recruitment and reductions in primary tumors a

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

100 nal adhesion molecule C (JAM-C) in mediating leukocyte recruitment and retention in the RA joint.

101 Pulmonary leukocyte recruitment and splenic or pulmonary T cell cy

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

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

104 trix metalloproteinases (MMPs) in modulating leukocyte recruitment and the potentially indiscriminate

105 /3 in mast cells decreased the IL-33-induced leukocyte recruitment and the resulting skin inflammatio

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

107 In contrast, leukocyte recruitment and tissue regeneration were unaff

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

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

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

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

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

113 uring bacterial proliferation, inflammation, leukocyte recruitment, and cellular apoptosis in Peyer's

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

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

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

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

118 of glomerulonephritis, CD74(+) and CXCR4(+) leukocyte recruitment, and proinflammatory cytokine and

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

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

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

122 esion 24 h after endotoxin challenge and new leukocyte recruitment as revealed both immunohistochemic

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

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

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

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

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

128 8/14 and TLR4 as important modulators of the leukocyte recruitment cascade during inflammation in viv

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

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

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

132 reasing efficiency of the first steps of the leukocyte recruitment cascade.

133 correlated with decreased polymorphonuclear leukocyte recruitment, chemokine and cytokine levels, ab

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

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

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

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

138 Leukocyte recruitment did not occur without coitus or wi

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

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

141 troctyes are critical in IL-17-Act1-mediated leukocyte recruitment during autoimmune-induced inflamma

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

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

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

145 Leukocyte recruitment during inflammation must be tightl

146 es and heparan sulfate (HS) is essential for leukocyte recruitment during inflammation.

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

148 Chemokines promote leukocyte recruitment during inflammation.

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

150 R mutation modulates integrin activation and 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 In adult mammals, leukocyte recruitment follows a well-defined cascade of

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

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

158 ysm (AAA), an inflammatory disease, involves leukocyte recruitment, immune responses, inflammatory cy

159 choline (OxPAPC) on chemokine expression and leukocyte recruitment in a facsimile synovium in vivo us

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 ntibody treatment exert disparate effects on leukocyte recruitment in inflamed joints.

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

165 prominent role of endothelial activation and leukocyte recruitment in lower-extremity arterial diseas

166 There are multiple drivers of leukocyte recruitment in lung allografts that contribute

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

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

169 Leukocyte recruitment in response to inflammatory signal

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

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

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

173 Leukocyte recruitment in the airways, cytokine levels, a

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

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

176 travital microscopy showed that platelet and leukocyte recruitment in the early stages of DVT was dra

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

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

179 did not alter the microbial burden or total leukocyte recruitment in the lung.

180 Leukocyte recruitment in thrombocytopenic mice remained

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

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

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

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

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

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

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

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

189 (-/-) mice, which correlated with defects in leukocyte recruitment including dendritic cells, NK cell

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

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

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

193 pe 2 diabetes is of adipose dysfunction with leukocyte recruitment into adipose leading to chronic in

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

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

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

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

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

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

200 matory bowel disease (IBD), its capacity for leukocyte recruitment into the gut, and the number of CX

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

202 Myeloid leukocyte recruitment into the lung in response to envir

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

204 To further define the role of chemokines in leukocyte recruitment into tumors, we evaluated anti-tum

205 Leukocyte recruitment is a central immune process.

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

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

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

209 Leukocyte recruitment is generally achieved by rapid mig

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

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

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

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

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

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

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

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

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

219 Therapies targeting leukocyte recruitment may be beneficial in reducing vasc

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

221 The anti-tumor effects and leukocyte recruitment mediated by anti-CD40 alone, were

222 y reduce inflammatory responses by targeting leukocyte recruitment mediated by extracellular cyclophi

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

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

225 ntrol in BMT mice is not related to impaired leukocyte recruitment or defective APC function.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 Leukocyte recruitment to inflammation sites progresses i

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

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

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

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

247 RATIONALE: Leukocyte recruitment to sites of allergic inflammation

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

249 Leukocyte recruitment to sites of infection or inflammat

250 Leukocyte recruitment to sites of inflammation is critic

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

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

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

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

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

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

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

258 tion in EIU animals significantly suppressed leukocyte recruitment to the anterior chamber, vitreous,

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

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

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

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

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

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

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

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

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

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

272 VCAM-1 is critical for T cell activation and leukocyte recruitment to the inflammation site and, ther

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

281 ss the cellular and regulatory mechanisms of leukocyte recruitment to the vessel wall in cardiovascul

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

283 zebrafish reveals a novel mechanism of early leukocyte recruitment to wounds through a concentration

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

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

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

289 Leukocyte recruitment was analyzed by intravital microsc

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