ライフサイエンスコーパス: leukocyte

1 s in response to the presence of an adhering leukocyte.

2 the alphaLbeta2-mediated rolling adhesion of leukocytes.

3 to resist killing by human polymorphonuclear leukocytes.

4 d infiltrating cells such as macrophages and leukocytes.

5 ed in female, but not male, human and murine leukocytes.

6 8(-/-) leukocytes extravasated later than WT leukocytes.

7 regions, which were enriched in infiltrating leukocytes.

8 ucing the recruitment of tissue-infiltrating leukocytes.

9 latelets can modulate the immune response of leukocytes.

10 e formation, and also formed aggregates with leukocytes.

11 elation between CXCR4 signal and presence of leukocytes.

12 o not play merely passive roles in activated leukocytes.

13 velopment leads to increased infiltration of leukocytes.

14 ng regeneration, along with Il4ra-expressing leukocytes.

15 eds of MHC-bound peptides from graft-derived leukocytes.

16 s of hemiketals E2 and D2 by activated human leukocytes.

17 tion has been the least explored amongst all leukocytes.

18 al upon challenge by human polymorphonuclear leukocytes.

19 and nonparenchymal cells, including CD45(+) leukocytes.

20 eases that are reflected by changes in blood leukocytes.

21 t, dendritic cells as the major infiltrating leukocytes.

22 Compared to WT leukocytes, CtsB(-/-) leukocytes accumulated in a higher number in angiogenic

23 The recruitment of blood leukocytes across the endothelium to sites of tissue inf

24 poxide intermediate LTA4 into LTB4, a potent leukocyte activating agent, while the aminopeptidase act

25 . coli-induced "oxidative burst," as well as leukocyte activation, without affecting host phagocytosi

26 and partly prevented increases in VCAM-1 and leukocyte adhesion after treatment with tumour necrosis

27 ion in the genetic absence of Coro1A impairs leukocyte adhesion and extravasation in inflamed cremast

28 L-selectin regulates leukocyte adhesion and rolling along the endothelium.

29 the effects of hemodynamics and cytokines on leukocyte adhesion and trans-endothelial migration (TEM)

30 3 cells, suggesting that these miRs regulate leukocyte adhesion by modulating the expression of adhes

31 activation on neutrophils is the hallmark of leukocyte adhesion deficiency (LAD) syndrome in humans,

32 Insulin decreased VCAM-1 expression and leukocyte adhesion in quiescent tumour endothelial cells

33 Using a leukocyte adhesion in vitro assay under shear forces mim

34 Leukocyte adhesion is mediated mainly by selectins, cell

35 The leukocyte adhesion receptor L-selectin forms bonds with

36 is study investigated the regulation of firm leukocyte adhesion to human brain endothelium by two dif

37 Leukocyte adhesion to P-selectin on activated platelets

38 studied endothelial permeability, intravital leukocyte adhesion, involvement of the Akt/WNT/beta-cate

39 by integrin-dependent sickle-red blood cell-leukocyte adhesion.

40 finity triggering mediates chemokine-induced leukocyte adhesion.

41 nted a higher number of circulating platelet-leukocyte aggregates, and neutrophils displayed a greate

42 Intrinsic vascular wall cells and lesional leukocytes alike can produce this cytokine.

43 Leukocyte alpha-galactosidase A enzyme activity was mild

44 Sokal score, increased spleen size, and high leukocyte and peripheral-blood blast counts.

45 to the vessel wall, where they interact with leukocytes and appear to seal gaps that arise between en

46 re-severe disease, but patients with low CSF leukocytes and cytokine concentrations were more likely

47 lammation, which including reduced influx of leukocytes and down regulated tumor-promoting cyto-/chem

48 either GM-CSF or its receptor recruit fewer leukocytes and function relatively well, whereas mice pr

49 CXCR3 axis has a critical role in recruiting leukocytes and inducing RGC death.

50 haracterized by massive transmural influx of leukocytes and lymphocytes, resulting in villous degener

51 However, MPs from leukocytes and monocytes origin were increased in CF pat

52 The TL gap between leukocytes and muscle (LTL-MTLA) was wider (P=0.0003), a

53 s wider (P=0.0003), and the TL ratio between leukocytes and muscle (LTL/MTLA) was smaller (P=0.0001)

54 Leukocytes and other amoeboid cells change shape as they

55 Leukocytes and pathogens can pass directly through the e

56 Association of host cells such as leukocytes and platelets with endothelia under vascular

57 nel by comparing HCC tissue and normal blood leukocytes and showed that methylation profiles of HCC t

58 the endothelium in regulating the passage of leukocytes and small molecules into the CNS has been stu

59 that the contractile stresses exerted by the leukocytes and the VECs can separately perturb the junct

60 of the 3D traction stresses generated by the leukocytes and VECs to elucidate the sequence of mechani

61 shifts in the composition of tissue-resident leukocytes and with an accumulation of activated CD4(+)

62 ctin glycoprotein ligand-1 (PSGL-1) on other leukocytes and with peripheral node addressin (PNAd) on

63 diminished proliferation of hepatocytes and leukocytes, and attenuated overall inflammatory response

64 charged phosphatidylserine (PS) on adherent leukocytes, and clot burden after 48 hours were signific

65 ies new associations between classical human leukocyte antigen (HLA) alleles and common immune-mediat

66 ymorphic genetic system in humans, the human leukocyte antigen (HLA) genes of the adaptive immune sys

67 ability to present neoantigens through human leukocyte antigen (HLA) loss may facilitate immune evasi

68 Then, three decades ago, an unusual human leukocyte antigen (HLA) molecule was identified: HLA-G.

69 Additionally, the human leukocyte antigen (HLA) region was comprehensively studi

70 ne, the C11orf30/LRRC32 locus, and the human leukocyte antigen (HLA) region.

71 kflow Language (CWL) implementation of human leukocyte antigen (HLA) typing using Polysolver or HLAmi

72 Identification of human leukocyte antigen (HLA)-bound peptides by liquid chromat

73 Human leukocyte antigen (HLA)-C*06:02 is identified as the all

74 f age in 715 children positive for the human leukocyte antigen (HLA)-DQ2 and/or HLA-DQ8 from 5 Europe

75 Human leukocyte antigen (HLA)-DQ2.5 (DQA1*05/DQB1*02) is a cla

76 s have reported an association between human leukocyte antigen (HLA)-DRB1 and the risk of PD.

77 Specific alleles of the human leukocyte antigen (HLA)-DRB1 gene (HLA-DRB1) encode a "s

78 estricted by the human MHC-Ib molecule human leukocyte antigen (HLA)-E and specific for an epitope fr

79 , we present loss of heterozygosity in human leukocyte antigen (LOHHLA), a computational tool to dete

80 e production and significantly reduced human leukocyte antigen - antigen D related expression.

81 onse to bacterial stimulation and less human leukocyte antigen - antigen D related.

82 ient presentation of tumor antigens by human leukocyte antigen class I (HLA-I) molecules.

83 n 38 (CD38) and CD69 but low levels of human leukocyte antigen DR, CD80, and CD86 at baseline.

84 egulated macrophage-derived chemokine, human leukocyte antigen DR, CD86, and CD80 correlated positive

85 class II antigen was replaced with the human leukocyte antigen DR4 (HLA-DR4).

86 immune tolerance mechanism induced by human leukocyte antigen G (HLA-G), was investigated.

87 olymorphism rs41269979 in the class II human leukocyte antigen region was more frequent in the invasi

88 nalysis to dissect associations in the human leukocyte antigen region, which suggests important roles

89 n tumor antigen NY-ESO-1 (ESO) and the human leukocyte antigen variant HLA-A*0201 (A2) as a model and

90 rategy relies on initial prediction of human leukocyte antigen-binding peptides by in silico algorith

91 extracellular diffusible ligands or require leukocyte antigen-related (Lar), a receptor protein tyro

92 an knockout (KO) pig cells and class I swine leukocyte antigens (SLA).

93 Before injury, leukocytes are near the vascular region, that is, approx

94 ulating a natural inhibitory receptor called leukocyte-associated Ig-like receptor-1 (LAIR-1).

95 s a threefold higher power output than other leukocyte biofuel cells.

96 More than 80% of the leukocyte blood gene expression response was similar in

97 (100 microg/ml) induced elevated complement, leukocyte CD11b and inflammatory mediators, and in Wista

98 , being expressed mostly in the infiltrating leukocytes (CD45(+) cells), including macrophages (F4/80

99 Activated leukocyte cell adhesion molecule (ALCAM) is a cell adhes

100 creased IFN-beta-mediated apoptosis of major leukocyte cell populations, including CD4(+) and CD8(+)

101 enin targets like glutamine synthetase (GS), leukocyte cell-derived chemotaxin 2, Regucalcin, and Cyc

102 A natural leukocyte chemoattractant was isolated from bovine serum

103 lted in a corresponding decrease in platelet-leukocyte complex formation and markedly reduced generat

104 t numbers, platelet activation, and platelet-leukocyte complex formation in the bronchoalveolar space

105 Leukocytes composed mainly of macrophages and neutrophil

106 ils were the main IL-4-producing endometrial leukocyte (constitutively and during Chlamydia infection

107 me, and more-precise characterization of CSF leukocytes could guide possible host-directed therapeuti

108 Leukocyte count and CD64 expression on neutrophils (nCD6

109 m, which predicted cerebrospinal fluid (CSF) leukocyte count and survival of Vietnamese patients with

110 association between house dust endotoxin and leukocyte count in a national survey.

111 natriuretic peptide, C-reactive protein, and leukocyte count.

112 ressure, lower ultrafiltration rates, higher leukocyte counts and neutrophil-to-lymphocyte ratios.

113 GF-beta1 were thus correlated with the total leukocyte counts in the synovial fluids.

114 lky disease, lower hemoglobin levels, higher leukocyte counts, and similar diffuse uptake in the sple

115 Compared to WT leukocytes, CtsB(-/-) leukocytes accumulated in a higher

116 106/l +/- 8.0 trauma, p < 0.05) and reduced leukocyte cytokine secretion in response to lipopolysacc

117 examined bronchoalveolar lavage (BAL) fluid leukocytes, cytokines, mediators, and epithelial cell fu

118 Leukocyte deconvolution analysis identifies changes in n

119 Time-dependent leukocyte density and diversity and the magnitude of myo

120 Post-MI leukocyte density, residence time in the infarcted area,

121 in nutritional as well as blood parameters, leukocyte depletion, and bone marrow hypoplasia.

122 gration (TEM) and subsequent accumulation of leukocyte-derived foam cells in the artery wall.

123 In contrast, BKV infection of leukocytes did elicit an antiviral response.

124 ic variants of APC were variably detected in leukocyte DNA and/or non-neoplastic intestinal mucosa of

125 and specific and it requires only 50 mug of leukocyte DNA isolated from 2-3 mL of blood to accuratel

126 38), the levels of dG-gx-dC and dG-gx-dA in leukocyte DNA were 1.94 +/- 1.20 and 2.10 +/- 1.77 in 10

127 chical clustering of patterns of age-related leukocyte dynamics.

128 molecule expression, resulting in attenuated leukocyte-endothelial interaction in vitro and in vivo a

129 s of acute ischaemic stroke, blocking of the leukocyte-endothelium adhesion by antagonism of alpha4 i

130 om these studies regarding the mechanisms of leukocyte entry into the kidney during inflammation and

131 C significantly enhanced the infiltration of leukocytes, especially T cells.

132 CTSD(-/-) leukocytes exhibited reduced cytokine release after lipo

133 Wild-type (WT) leukocytes extravasated from limbal vessels, angiogenic

134 CD18(-/-) leukocytes extravasated later than WT leukocytes.

135 e inflammatory response, cell proliferation, leukocyte extravasation and cholesterol biosynthesis.

136 esults reveal an unexpected role for CtsB in leukocyte extravasation and transmigration, which advanc

137 Moreover, leukocytes from 3 of the patients displayed defective IF

138 s II molecule type loaded with peptides from leukocytes from the graft.

139 e functions (e.g., immune system activation, leukocyte function, macrophage response) were preferenti

140 during pneumonia-derived sepsis by enhancing leukocyte function.

141 suggested to mediate the differentiation of leukocytes; however, their intrinsic, direct regulation

142 immune changes are usually measured in blood leukocytes; however, this might not reflect alterations

143 endotoxin challenge, the clonal response of leukocytes in bone marrow of acute myeloid leukaemia (AM

144 studies have reported increased inflammatory leukocytes in circulation of individuals with stress-rel

145 Leukocytes in CSWB-treated blood exhibited significantly

146 The role of the circulating leukocytes in lungs and their relationship with circulat

147 ffects irrespective of the presence of human leukocytes in mice.

148 Leukocytes in murine hearts, pericardial AT, spleen, med

149 l showed pyrimethamine lowers SOD1 levels in leukocytes in patients with SOD1 mutations.

150 egions and had strikingly reduced numbers of leukocytes in the bronchoalveolar lavage fluid and lower

151 were directly proportional to the number of leukocytes in the range of 0.028-4.2 U L(-1) (9-690 mug

152 id not reduce the proportion of infiltrating leukocytes in the tumor microenvironment but altered the

153 In addition, the presence of human leukocytes increased the expression of cytokines and che

154 METHODS AND Leukocytes infiltrating the failing heart were analyzed

155 tion with HA, generates an ECM that promotes leukocyte infiltration and adhesion.

156 n protein 1 (VCAM-1), molecules that mediate leukocyte infiltration and are associated with inflammat

157 e Marsh classification and characterized for leukocyte infiltration and MC distribution.

158 ion of etifoxine was associated with reduced leukocyte infiltration into the brain and microglial pro

159 rized by disruption of the BBB and increased leukocyte infiltration into the CNS.

160 o myocardial infarction (MI), time-dependent leukocyte infiltration is critical to program the acute

161 eficient mice showed reduced tubular injury, leukocyte infiltration, and inflammation following renal

162 ic nephropathy by inducing genes involved in leukocyte infiltration, cell proliferation, and extracel

163 ry membrane thickening and polymorphonuclear leukocyte infiltration, reduced NF-kappaB translocation

164 xpressed genes associated with inhibition of leukocyte infiltration.

165 extensively characterized and implicated in leukocyte inflammatory and immune functions, the roles o

166 The leukocyte integrin alphaMbeta2 (CR3 or Mac-1) has both p

167 The leukocyte integrin Mac-1 (also known as integrin alphaMb

168 Recognition by the leukocyte integrins alphaXbeta2 and alphaMbeta2 of compl

169 ed the edema, migration of polymorphonuclear leukocytes into the peritoneal cavity, as well as abdomi

170 hair cell ablation is sufficient to attract leukocytes into the spiral ganglion, and that fractalkin

171 tolerated dose increases the infiltration of leukocytes into the tumor, slowing tumor growth and prev

172 Here, we hypothesized that excessive leukocyte invasion leads to heart failure and death duri

173 ine that regulates adhesion and migration of leukocytes is expressed by SGNs and signals to leukocyte

174 How Duox establishes long-range signaling to leukocytes is unclear.

175 flammatory mediator production by peritoneal leukocytes isolated from the peritoneal dialysis effluen

176 We analyzed: (1) peripheral blood leukocyte levels and immune responses; and (2) RNA seque

177 We hypothesized that transfusion of leukocytes loaded ex vivo with the lipophilic antifungal

178 number of inflammatory mediators released by leukocytes, mainly neutrophils, upon bacterial challenge

179 indings suggest that posaconazole-loading of leukocytes may hold promise for the therapy of IPA.

180 healthy volunteers were evaluated for blood leukocyte mCD48 expression and sCD48 in serum.

181 , and TIPE2-deficient mice were resistant to leukocyte-mediated neural inflammation.

182 Chemokines are the principal regulators of leukocyte migration and are essential for initiation and

183 or near genes involved in cellular adhesion, leukocyte migration and atherosclerosis (PECAM1, rs18676

184 The chemokine receptor CCR7 drives leukocyte migration into and within lymph nodes (LNs).

185 llowing infection and for the restriction of leukocyte migration into the brain.

186 conditions, as well as in various diseases, leukocyte migration is a crucial issue for the immune sy

187 production, intracellular antioxidation, and leukocyte migration plus genes for proinflammatory cytok

188 f the ImmunoCloak also significantly reduced leukocyte migration through the endothelial cell layer b

189 The effect of strawberry extract and P3G, on leukocyte migration, exudation levels and many inflammat

190 ribed, chronic environmental determinants of leukocyte number are less well understood.

191 ene expression profiling in peripheral blood leukocytes of adult patients admitted to intensive care

192 gonists were impaired in the fibroblasts and leukocytes of all TIRAP-deficient individuals.

193 ession and DNA methylation profiles in blood leukocytes of apparently healthy smokers predicts with r

194 merase reverse transcriptase (TERT) in blood leukocytes of approximately 5% of individuals with inher

195 peroxidase (MPO) and proteinase 3 (PRTN3) in leukocytes of patients with ANCA-associated vasculitis o

196 from bronchoalveolar lavage (BAL) cells and leukocytes of sarcoidosis patients.

197 weakly cytotoxic towards human primary blood leukocytes or retinal pigment epithelial cells at effect

198 ized by low infiltration of tumor-associated leukocytes, particularly macrophages and CD8(+) T cells,

199 tor protein Src homology 2 domain-containing leukocyte phosphoprotein of 76 kDa (SLP-76) plays a cruc

200 13-Series resolvins mediate the leukocyte-platelet actions of atorvastatin and pravastat

201 It incorporates leukocytes, platelets, and growth factors within the den

202 Increased levels of leukocytes, platelets, and tissue factor-positive (TF(+)

203 hematologic and renal toxicity (hemoglobin, leukocytes, platelets, creatinine), and immunohistochemi

204 s inflammation by reducing polymorphonuclear leukocyte (PMN) recruitment to the affected organs.

205 Human neutrophils (polymorphonuclear leukocytes [PMNs]) generate inflammatory responses withi

206 We found here that leukocyte polarity was generated by TIPE2 (TNFAIP8L2), a

207 ptors that are expressed on many of the same leukocyte populations and bind many of the same ligands.

208 protein levels were investigated in distinct leukocyte populations from PD patients with depression a

209 al sampling of multiple tissues and enriched leukocyte populations from SIVmac251-infected macaques w

210 surfaces that allow the capture of distinct leukocyte populations from small volumes blood using cam

211 ruli have identified glomerulus-infiltrating leukocyte populations in NZM2328 (NZM) lupus-prone mice

212 Functionally similar leukocyte populations were grouped by using unbiased hie

213 two OPN isoforms in causing the imbalance of leukocyte populations.

214 hesion to vascular endothelial cells (VECs), leukocytes preferentially extravasate across junctional

215 IL-10 concentration and regulatory T cell-to-leukocyte ratio in RIPK3 knockout mice.

216 ion and elongation protein zeta 2 (fez2) and leukocyte receptor cluster (lrc) member, two genes ident

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

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

219 Leukocyte recruitment and activation within the lungs we

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

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

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

223 Chemokines promote leukocyte recruitment during inflammation.

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

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

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

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

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

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

230 ction exacerbates endothelial exocytosis and leukocyte recruitment.

231 The endotoxin-leukocyte relationship was evaluated by linear regressio

232 PTN has been shown to promote leukocyte responses by inducing their migration and expr

233 Stromal cells regulate leukocyte responses in lymph nodes, but the role of stro

234 caused by activating mutations in either the leukocyte-restricted p110delta catalytic (PIK3CD) subuni

235 n nitrate-fed mice there is reduced systemic leukocyte rolling and adherence, circulating neutrophil

236 sive imaging revealed a dramatic increase in leukocyte rolling and adhesion in veins near the optic n

237 ions with fucosylated glycan ligands mediate leukocyte rolling in the vasculature under shear forces.

238 tomography and computed tomography, labeled leukocyte scintigraphy (LS), and Gallium-67 citrate scin

239 Deleting CXCR3 in leukocytes significantly reduced leukocyte recruitment,

240 In polymorphonuclear leukocytes, SipA or other Salmonella pathogenicity islan

241 We show that mechanisms mediating leukocyte slow rolling and emigration are impaired in Ga

242 Leukocyte-specific integrin alphaDbeta2 (CD11d/CD18) is

243 We analyzed HK biosynthesis in human leukocytes stimulated ex vivo and defined the biosynthet

244 d the detection of ZIKV antigen in a defined leukocyte subset from patients' whole-blood specimens.

245 tudy identifies specific dynamic patterns of leukocyte subset numbers, as well as nongenetic determin

246 ffects modeling to define the dynamics of 62 leukocyte subsets from birth to 6 years of age in 1182 c

247 ermal cell proliferation, and recruitment of leukocyte subsets into the skin.

248 specific cytokine environments and activated leukocyte subsets.

249 a-arrestins, and is widely expressed by many leukocyte subsets.

250 by regulating the accumulation of pathogenic leukocyte subtypes, which drive the fibrotic response.

251 uman-derived peptides differentially stained leukocytes, suggesting peptide-dependent engagement.

252 a that GM-CSF is a major orchestrator of the leukocyte supply chain during inflammation.

253 Leukocyte telomere length (LTL) was measured with the us

254 We studied the associations of leukocyte telomere length (LTL) with all-cause, cardiova

255 ross-sectional associations of mean relative leukocyte telomere length (LTL) with objective measures

256 essed the association of sedentary time with leukocyte telomere length (LTL).

257 LE: Observational studies have found shorter leukocyte telomere length (TL) to be a risk factor for c

258 crosis factor, interleukin 1beta, 6, and 10, leukocyte telomere length, chronic disease status, and f

259 (95% CI, -14.1% to -3.1%) shorter cord blood leukocyte telomeres and 13.2% (95% CI, -19.3% to -6.7%)

260 considers wall shear stress (WSS) dependent leukocyte TEM and compensatory arterial remodeling obeyi

261 Moreover, using the model, we have found leukocyte TEM increases monotonically with decreases in

262 -infected SCs exhibited enhanced adhesion of leukocytes that correlated with decreases in SCB integri

263 response to adversity (CTRA) in circulating leukocytes that may contribute to social gradients in di

264 As compared to direct assays of plasma or leukocytes, the EV detection rate was significantly enha

265 For total leukocytes, there was suggestive evidence in the ALHS of

266 n in TME comprising overt tumor-infiltrating leukocytes (TILeus) induces systemic antitumor immunity

267 reduced the profibrotic responses of uremic leukocytes to endogenous components present in the PDE o

268 le complexes lead to enhanced recruitment of leukocytes to inflamed tissue.

269 However, the differential response of human leukocytes to MPLA and LPS has not been well characteriz

270 feature of sepsis is the reduced capacity of leukocytes to release proinflammatory cytokines in respo

271 ut that platelets support the recruitment of leukocytes to sites of inflammation.

272 kines, thereby inhibiting the recruitment of leukocytes to the location of the tick bite.

273 cifically inhibiting the response of myeloid leukocytes to the pathogen.

274 flammatory lesions, presumably by preventing leukocyte trafficking from the periphery.

275 The role of sphingosine-1 phosphate (S1P) in leukocyte trafficking has been well deciphered in mice b

276 to determine the role of GPBAR1 in mediating leukocyte trafficking in chemically induced models of co

277 vasive, cost-effective method to investigate leukocyte trafficking in the tumor microenvironment, but

278 However, once extravasated, CD18(-/-) leukocytes transmigrated more rapidly than their WT coun

279 that was previously shown to be involved in leukocyte transmigration across the endothelium.

280 Leukocyte transmigration across vessel walls is a critic

281 ng at the cellular level in order to predict leukocyte transmigration and plaque evolution.

282 ticularly in the CNS, where inflammation and leukocyte transmigration must be tightly regulated.

283 CAM-1-mediated adhesion to prevent excessive leukocyte transmigration remain unknown.

284 the opening of gaps before the initiation of leukocyte transmigration.

285 iated with, but TspanC8s remain unstudied in leukocyte transmigration.

286 ession of endothelial adhesion molecules and leukocyte transmigration.

287 permeability and inflammation that influence leukocyte transport across the BBB.

288 n transmigration of freshly isolated primary leukocytes under flow has not been demonstrated, and the

289 ctive protein (CRP) values, haemoglobin, and leukocyte values.

290 ukocytes is expressed by SGNs and signals to leukocytes via its receptor CX3 CR1.

291 il preservative is described that stabilizes leukocyte viability and erythrocyte morphology in whole

292 ME recruitment of leukocytes was delayed but persisted far longer than in

293 RNA from isolated blood leukocytes was used for quantitative polymerase chain re

294 ue partitioning by intravascular staining of leukocytes, we showed that both inflammatory and residen

295 Consequently, TIPE2-deficient leukocytes were defective in polarization and chemotaxis

296 chemokine receptor utilized by HIV to infect leukocytes, whereas CCR5 ligands inhibit infection by bl

297 ibroblasts, myofibroblasts, macrophages, and leukocytes with a reduction in Tnf-alpha gene expression

298 was significantly enhanced by co-culture of leukocytes with cell lines prior to molecular and immuno

299 Activation of leukocytes with LPS followed by treatment with the calci

300 Erythrocyte and leukocyte zinc concentrations and zinc transporter expre