ライフサイエンスコーパス: intercellular adhesion molecule

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1 evirus A21, an EV with tropism for the human intercellular adhesion molecule 1 (hICAM-1), through ser

2 thelial growth factor (VEGF)), inflammatory (intercellular adhesion molecule 1 (ICAM-1) and cyclooxyg

3 human melanoma cell line (Lu1205) increased intercellular adhesion molecule 1 (ICAM-1) and E-selecti

4 We find that intercellular adhesion molecule 1 (ICAM-1) and ICAM-2 on

5 e endothelium and in adhesion to immobilized intercellular adhesion molecule 1 (ICAM-1) and vascular

6 ed protein kinases (MAPKs) and expression of intercellular adhesion molecule 1 (ICAM-1) and vascular

7 the proinflammatory cell adhesion molecules intercellular adhesion molecule 1 (ICAM-1) and vascular

8 ction associated antigen 1 (LFA-1) binds the intercellular adhesion molecule 1 (ICAM-1) by its alpha(

9 In this study, the binding affinity of human intercellular adhesion molecule 1 (ICAM-1) chimera and l

10 ezrin/radixin/moesin (ERM) phosphorylation, intercellular adhesion molecule 1 (ICAM-1) clustering, a

11 Infected IL-17R-deficient corneas had low intercellular adhesion molecule 1 (ICAM-1) expression, a

12 Intercellular adhesion molecule 1 (ICAM-1) is a cell-sur

13 The intercellular adhesion molecule 1 (ICAM-1) is induced in

14 ascular cell adhesion molecule (VCAM-1), and intercellular adhesion molecule 1 (ICAM-1) on endothelia

15 to LLV was able to trigger the clustering of intercellular adhesion molecule 1 (ICAM-1) on endothelia

16 scribed as an inflammatory disease, in which intercellular adhesion molecule 1 (ICAM-1) plays a key r

17 re we show that HDL suppresses expression of intercellular adhesion molecule 1 (ICAM-1) through the t

18 shown to bind to several receptors, of which intercellular adhesion molecule 1 (ICAM-1) upregulation

19 the NF-kappaB pathway instantly upregulates intercellular adhesion molecule 1 (ICAM-1) which binds i

20 This is the case for intercellular adhesion molecule 1 (ICAM-1), a glycoprote

21 ction also increased the cellular content of intercellular adhesion molecule 1 (ICAM-1), a molecule i

22 ow a group of PfEMP1 proteins interacts with intercellular adhesion molecule 1 (ICAM-1), allowing us

23 rogenic TGRL increased expression of VCAM-1, intercellular adhesion molecule 1 (ICAM-1), and E-select

24 Leukocyte infiltration, improved levels of intercellular adhesion molecule 1 (ICAM-1), and oxidativ

25 tenuated the over expression of VEGF and the intercellular adhesion molecule 1 (ICAM-1), and reduced

26 gnificant in only 1 replication set included intercellular adhesion molecule 1 (ICAM-1), anti-LG3, am

27 "outside-in" signaling when bound to ligand intercellular adhesion molecule 1 (ICAM-1), but little i

28 vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule 1 (ICAM-1), E-selectin,

29 d inflammation: coagulation factor III (F3), intercellular adhesion molecule 1 (ICAM-1), interferon g

30 tu-like expression of cadherins, E-selectin, intercellular adhesion molecule 1 (ICAM-1), vascular cel

31 We examined human effector T lymphocytes on intercellular adhesion molecule 1 (ICAM-1)-coated surfac

32 l host factors impacting protection included intercellular adhesion molecule 1 (ICAM-1)-dependent pol

33 cell morphology alterations, and crawling on intercellular adhesion molecule 1 (ICAM-1)-expressing ce

34 that is enhanced by the binding of LFA-1 to intercellular adhesion molecule 1 (ICAM-1).

35 nt/beta-catenin signaling in AECs attenuated intercellular adhesion molecule 1 (ICAM-1)/vascular cell

36 d proteins HLA-A, HLA-B, and HLA-C antigens; intercellular adhesion molecule 1 (ICAM-1); S100; transc

37 nregulate MHC-I and PECAM-I but not B7.2 and intercellular adhesion molecule 1 (ICAM-I), consistent w

38 in T cells increased expression of IFNG and intercellular adhesion molecule 1 (ICAM1) and induced T-

39 , unlike amphiregulin and TNFRI, full-length intercellular adhesion molecule 1 (ICAM1) is released fr

40 pression of asparaginyl endopeptidase (AEP), intercellular adhesion molecule 1 (ICAM1), and ras-relat

41 monocyte chemoattractant protein-1 (MCP-1), intercellular adhesion molecule 1 (ICAM1), F4/80, plasmi

42 out mice originated from decreased levels of intercellular adhesion molecule 1 (ICAM1)/vascular cell

43 s, hepatic decompensation, and soluble serum intercellular adhesion molecule 1 (sICAM-1) MFI.

44 otein (hs-CRP), adiponectin, leptin, soluble intercellular adhesion molecule 1 (sICAM-1), soluble vas

45 or, neutrophil count, IL-1alpha, E-selectin, intercellular adhesion molecule 1 [ICAM-1], myeloperoxid

46 IL-6], IL-8, IL-1alpha, CXCL1, CXCL2, CXCL3, intercellular adhesion molecule 1 [ICAM1]), chemoattract

47 s and to enhanced cell-surface expression of intercellular adhesion molecule 1 and altered expression

48 stained positive for 2 inflammatory markers, intercellular adhesion molecule 1 and interleukin 8.

49 Unexpectedly, other proteins, including intercellular adhesion molecule 1 and moesin, were selec

50 L oxidation and 2) a significant decrease in intercellular adhesion molecule 1 and OLR1 gene expressi

51 Soluble intercellular adhesion molecule 1 and soluble vascular c

52 munoblots were used to measure expression of intercellular adhesion molecule 1 and the inducible form

53 n the luminal surface, such as clustering of intercellular adhesion molecule 1 and vascular cell adhe

54 derived from clustering of apically disposed intercellular adhesion molecule 1 and vascular cell adhe

55 apitulated when a combination of recombinant intercellular adhesion molecule 1 and vascular cell adhe

56 dies against Macrophage-1 antigen (Mac-1) or intercellular adhesion molecule 1 and were reproduced in

57 ion of NF-kappaB, which in turn up-regulated intercellular adhesion molecule 1 as evident from chroma

58 D showed increased endothelial inflammation (intercellular adhesion molecule 1 expression) and increa

59 -1 displayed an attenuated interleukin-6 and intercellular adhesion molecule 1 expression, resulting

60 atter correlated with diastolic function and intercellular adhesion molecule 1 expression.

61 reactive protein, interleukin 6, and soluble intercellular adhesion molecule 1 in plasma.

62 the lymphocyte function-associated antigen 1-intercellular adhesion molecule 1 interaction, reduced T

63 nduced expression of MHC-I, MHC-II, and CD54/intercellular adhesion molecule 1 molecules.

64 but involved class II histocompatibility and intercellular adhesion molecule 1 molecules.

65 cantly increased KC numbers via induction of intercellular adhesion molecule 1 on liver sinusoidal en

66 the expression of endothelial E-selectin and intercellular adhesion molecule 1 was decreased by eithe

67 6, tumor necrosis factor alpha, and soluble intercellular adhesion molecule 1 were measured.

68 Focusing on intercellular adhesion molecule 1(ICAM)-1 as a model, we

69 e function-associated antigen 1) for ICAM-1 (intercellular adhesion molecule 1) but significantly low

70 n 6, tumor necrosis factor alpha and soluble intercellular adhesion molecule 1) were unsuitable for p

71 Deficiency of intercellular adhesion molecule 1, a counter-receptor fo

72 The expression of intercellular adhesion molecule 1, an NF-kappaB-dependen

73 phaIIbbeta3 with endothelial alphavbeta3 and intercellular adhesion molecule 1, and (3) a stimulatory

74 4 BCC tumor mRNA markers (CD25, CD3epsilon, intercellular adhesion molecule 1, and CD68) that have b

75 lpha, interleukin (IL)-1beta, IL-6, KC/IL-8, intercellular adhesion molecule 1, and cluster of differ

76 active protein, adiponectin, leptin, soluble intercellular adhesion molecule 1, and E-selectin all fe

77 s showed increased interleukin (IL)-6, IL-8, intercellular adhesion molecule 1, and platelet endothel

78 elated adhesion molecules (e.g., P-selectin, intercellular adhesion molecule 1, and vascular cell adh

79 anulocyte colony-stimulating factor, soluble intercellular adhesion molecule 1, macrophage migration-

80 selectin, vascular cell adhesion molecule 1, intercellular adhesion molecule 1, platelet endothelial

81 ceptor-2, vascular cell adhesion molecule 1, intercellular adhesion molecule 1, selectins, and integr

82 orrelated with IL-6, soluble TNF receptor 2, intercellular adhesion molecule 1, vascular adhesion mol

83 ld increase in the expression of E-selectin, intercellular adhesion molecule 1, vascular cell adhesio

84 sinophils also showed enhanced expression of intercellular adhesion molecule 1, which depended on dir

85 s also associated with the overexpression of intercellular adhesion molecule 1, which is expressed on

86 ng Raman-active molecules were conjugated to intercellular adhesion molecule 1- (ICAM-1-) specific mo

87 MP uptake is partly intercellular adhesion molecule 1-dependent and leads to

88 induced pulmonary inflammation, with altered intercellular adhesion molecule 1-dependent slow neutrop

89 g receptors DC-SIGN (dendritic-cell-specific intercellular adhesion molecule 1-grabbing nonintegrin;

90 gands, vascular cell adhesion molecule 1 and intercellular adhesion molecule 1.

91 orce-dependent kinetics of dissociation from intercellular adhesion molecule 1.

92 ntiation, respectively; the plasma levels of intercellular adhesion molecule 1; and CCR6 expression i

93 th factor beta1 and beta2; thrombospondin 2; intercellular adhesion molecule 1; interleukin 6 [IL-6];

94 rs of endothelial adhesion (sICAM-1 [soluble intercellular adhesion molecule 1] and sVCAM-1 [soluble

95 The major ligands of LFA-1 include three intercellular adhesion molecules 1, 2, and 3 (ICAM 1, 2,

96 creased vascular inflammation marker soluble intercellular adhesion molecule-1 (-10%, P < 0.01).

97 r alpha receptor II (B = 0.07, p < .01), and intercellular adhesion molecule-1 (B = 0.04, p < .05) le

98 efined as CD146(+)CD45(-)) exhibit increased intercellular adhesion molecule-1 (CD54) and Fas in resp

99 NOS), nuclear factor-kappa B (NF-kappaB) and intercellular adhesion molecule-1 (ICAM) (P < 0.001, res

100 of constitutive as well as IL-1beta-induced intercellular adhesion molecule-1 (ICAM-1) (of 55% and 5

101 ) to circulating pro-inflammatory cytokines, intercellular adhesion molecule-1 (ICAM-1) and acute cor

102 f these cells, concomitant with reduction of intercellular adhesion molecule-1 (ICAM-1) and diminishi

103 contact points for the known HRV receptors, intercellular adhesion molecule-1 (ICAM-1) and low-densi

104 t3 interaction in correlation with increased intercellular adhesion molecule-1 (ICAM-1) and soluble-I

105 lls, we found that GPx-1 deficiency augments intercellular adhesion molecule-1 (ICAM-1) and vascular

106 otential of these cells through reduction of intercellular adhesion molecule-1 (ICAM-1) and vascular

107 tic cell line THP-1 to a surface coated with intercellular adhesion molecule-1 (ICAM-1) as a function

108 udy was to identify mechanisms through which intercellular adhesion molecule-1 (ICAM-1) augments the

109 Intercellular adhesion molecule-1 (ICAM-1) contains five

110 We have previously shown that intercellular adhesion molecule-1 (ICAM-1) expressed by

111 tumor necrosis factor-alpha (TNF-alpha) and intercellular adhesion molecule-1 (ICAM-1) in aqueous hu

112 Here, the role of epithelial intercellular adhesion molecule-1 (ICAM-1) in gammadelta

113 Herein, we describe the overexpression of intercellular adhesion molecule-1 (ICAM-1) in human TNBC

114 ntigen-1 (LFA-1) interaction with its ligand intercellular adhesion molecule-1 (ICAM-1) induces a gen

115 sion and display high spontaneous binding to intercellular adhesion molecule-1 (ICAM-1) ligand under

116 yte function-associated antigen-1 (LFA-1) to intercellular adhesion molecule-1 (ICAM-1) mediates leuk

117 Intercellular adhesion molecule-1 (ICAM-1) mediates the

118 tumor necrosis factor alpha (TNFalpha), and intercellular adhesion molecule-1 (ICAM-1) messenger RNA

119 n species accumulation, CD14 expression, and intercellular adhesion molecule-1 (ICAM-1) mRNA and prot

120 recognition of pMHC and the adhesion ligand intercellular adhesion molecule-1 (ICAM-1) on supported

121 P-selectin and intercellular adhesion molecule-1 (ICAM-1) participate i

122 PfEMP1 and human endothelial proteins CD36, intercellular adhesion molecule-1 (ICAM-1), and endothel

123 tor inhibitor-1, soluble E-selectin, soluble intercellular adhesion molecule-1 (ICAM-1), and soluble

124 elial migration mediated by a combination of intercellular adhesion molecule-1 (ICAM-1), vascular adh

125 t endothelial adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1), vascular adh

126 pha by restraining the induced expression of intercellular adhesion molecule-1 (ICAM-1), vascular cel

127 sation requires selectin-mediated tethering, intercellular adhesion molecule-1 (ICAM-1)-dependent fir

128 ogo-B regulates leukocyte transmigration and intercellular adhesion molecule-1 (ICAM-1)-dependent sig

129 ated neutrophils, microglia/macrophages, and intercellular adhesion molecule-1 (ICAM-1)-positive bloo

130 otein that interacts with the host receptor, intercellular adhesion molecule-1 (ICAM-1).

131 ) in a low affinity state to slow rolling on intercellular adhesion molecule-1 (ICAM-1).

132 ression was notable in blood vessels, as was intercellular adhesion molecule-1 (ICAM-1).

133 immunohistochemically for the expression of intercellular adhesion molecule-1 (ICAM-1).

134 of the endothelial mechanosensitive receptor intercellular adhesion molecule-1 (ICAM-1).

135 protein (LDL) cholesterol, triglyceride, and intercellular adhesion molecule-1 (ICAM-1).

136 kers human leukocyte antigen-DR (HLA-DR) and intercellular adhesion molecule-1 (ICAM-1).

137 dhesion molecules in the vasculature such as intercellular adhesion molecule-1 (ICAM-1).

138 urface proteins, including CD69, L-selectin, intercellular adhesion molecule-1 (ICAM-1, CD54), CD44,

139 ster of differentiation 8a (Cd8a), Cd14, and intercellular adhesion molecule-1 (Icam1) by about two-f

140 ells so modified expressed reduced levels of intercellular adhesion molecule-1 (ICAM1; CD54); blockad

141 the prospective association between soluble intercellular adhesion molecule-1 (sICAM-1) and cancer r

142 dence of proliferative DR (PDR), and soluble intercellular adhesion molecule-1 (sICAM-1) and TNF-alph

143 active protein (CRP), serum amyloid A (SAA), intercellular adhesion molecule-1 (sICAM-1) and vascular

144 e measured levels of UA and soluble forms of intercellular adhesion molecule-1 (sICAM-1), vascular ce

145 generate polyplexes carrying siRNA targeting intercellular adhesion molecule-1 (siICAM-1).

146 Ld plus costimulatory ligands, i.e. B7-1 and intercellular adhesion molecule-1 along with 2C T cell r

147 h-sensitivity C-reactive protein and soluble intercellular adhesion molecule-1 and adjusted for these

148 Clinical risk factors, soluble intercellular adhesion molecule-1 and endocan (both form

149 [sRAGE]) and endothelial biomarkers (soluble intercellular adhesion molecule-1 and endocan [full-leng

150 n, including the metastasis-related proteins intercellular adhesion molecule-1 and urokinase-type pla

151 The lymphatic endothelium expresses intercellular adhesion molecule-1 and vascular adhesion

152 We also measured the expression of intercellular adhesion molecule-1 and vascular cell adhe

153 A1 exon skipping mutations had higher plasma intercellular adhesion molecule-1 and vascular cell adhe

154 , CCL5, and CCL20 and the adhesion molecules intercellular adhesion molecule-1 and vascular cell adhe

155 re, CB2R agonists decreased the induction of intercellular adhesion molecule-1 and vascular cell adhe

156 alpha receptor II) and endothelial function (intercellular adhesion molecule-1 and vascular cell adhe

157 derived from clustering of apically disposed intercellular adhesion molecule-1 and vascular cell adhe

158 ference studies identified interleukin-6 and intercellular adhesion molecule-1 as key NF-kappaB targe

159 in alpha(L)beta(2)-dependent slow rolling on intercellular adhesion molecule-1 by activating Src fami

160 We hypothesized that the expression of intercellular adhesion molecule-1 even in vessels with h

161 ced tumor necrosis factor (TNF)alpha-induced intercellular adhesion molecule-1 expression and attenua

162 eling-positive cells, TNF-alpha release, and intercellular adhesion molecule-1 expression compared wi

163 tes monocyte adhesion by inducing VCAM-1 and intercellular adhesion molecule-1 expression in endothel

164 leased platelet miR-320b on endothelial cell intercellular adhesion molecule-1 expression was shown.

165 reased vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression, and neutro

166 Removal of P-Rex1 significantly reduced intercellular adhesion molecule-1 expression, polymorpho

167 anism and induced an increase in endothelial intercellular adhesion molecule-1 expression, production

168 helial vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression, reduced in

169 HUVEC intercellular adhesion molecule-1 expression, stiffness,

170 treatment failed to inhibit TNFalpha-induced intercellular adhesion molecule-1 expression, treatment

171 he effect of adiponectin on TNFalpha-induced intercellular adhesion molecule-1 expression.

172 on, and endothelial activation, monitored by intercellular adhesion molecule-1 expression.

173 nduced vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression.

174 ges have been assumed to mediate adhesion to intercellular adhesion molecule-1 for T-cell conjugation

175 signaling were quite distinct so that LFA-1/intercellular adhesion molecule-1 interaction exerted a

176 antibody crosslinking or by crosslinking its intercellular adhesion molecule-1 ligand on the supporte

177 ses in vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 mRNA expression in the

178 Intercellular adhesion molecule-1 on melanoma cells and

179 Blocking intercellular adhesion molecule-1 prevents cellular egre

180 es produced greater levels of chemokines and intercellular adhesion molecule-1 that are associated wi

181 Binding of intercellular adhesion molecule-1 to the beta2-integrin

182 spleen tyrosine kinase and cell adhesion to intercellular adhesion molecule-1 under dynamic flow.

183 and expression of constitutive and inducible intercellular adhesion molecule-1 was significantly high

184 g/L (P<0.0001), and median levels of soluble intercellular adhesion molecule-1 were 374 versus 333 ng

185 n-8, monocyte chemoattactrant protein-1, and intercellular adhesion molecule-1 were analyzed after tr

186 uced pulmonary adhesion molecule expression (intercellular adhesion molecule-1) and tissue infiltrati

187 MC releasate elevated ICAM-1 (intercellular adhesion molecule-1) expression on HUVEC (

188 activator [tPA]) and endothelial activation (intercellular adhesion molecule-1) in serial biopsies ob

189 ascular cell adhesion molecule-1 and soluble intercellular adhesion molecule-1) were measured.

190 ons of vascular cell adhesion molecule-1 and intercellular adhesion molecule-1, albeit less efficient

191 lasma levels of tumor necrosis factor-alpha, intercellular adhesion molecule-1, and C-reactive protei

192 rom levels of C-reactive protein and soluble intercellular adhesion molecule-1, and endothelial funct

193 ssion of vascular endothelial growth factor, intercellular adhesion molecule-1, and tumor necrosis fa

194 rosis factor-alpha levels as well as cardiac intercellular adhesion molecule-1, cytokine-induced neut

195 unds of RW decreased serum concentrations of intercellular adhesion molecule-1, E-selectin, and IL-6

196 expression of NF-kappaB target genes VCAM-1, intercellular adhesion molecule-1, E-selectin, and tissu

197 rial loads were associated with higher serum intercellular adhesion molecule-1, E-selectin, and vascu

198 selectin, vascular cell adhesion molecule-1, intercellular adhesion molecule-1, fibrinogen-like prote

199 Soluble intercellular adhesion molecule-1, IFN-lambda1, and eosi

200 nd inflammatory markers [C-reactive protein, intercellular adhesion molecule-1, interleukin-6, and tu

201 high-sensitivity C-reactive protein, soluble intercellular adhesion molecule-1, leptin, hemoglobin A(

202 osis protein-2, cyclin D1, cyclooxygenase-2, intercellular adhesion molecule-1, matrix metalloprotein

203 Model 3 identified a set of 6 biomarkers (intercellular adhesion molecule-1, matrix metalloprotein

204 iomarkers strongly associated with death/MI: intercellular adhesion molecule-1, matrix metalloprotein

205 enofibrate also attenuated overexpression of intercellular adhesion molecule-1, monocyte chemoattract

206 ession of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, monocyte chemoattract

207 ut reduced expression or secretion of T-bet, intercellular adhesion molecule-1, nucleotide-binding ol

208 sitivity C-reactive protein, fibrinogen, and intercellular adhesion molecule-1, suggested that GlycA

209 or necrosis factor-alpha, interleukin-6, and intercellular adhesion molecule-1, than iron-overloaded

210 e chemotactic protein-1, C-reactive protein, intercellular adhesion molecule-1, vascular cell adhesio

211 ecreted levels of the proangiogenic proteins intercellular adhesion molecule-1, vascular cell adhesio

212 (tumor necrosis factor-alpha, interleukin-6, intercellular adhesion molecule-1, vascular cell adhesio

213 gamma), endothelial cell adhesion molecules (intercellular adhesion molecule-1, vascular cell adhesio

214 ay and expression of cell adhesion molecules intercellular adhesion molecule-1, vascular cell adhesio

215 , enhanced expression of adhesion molecules (intercellular adhesion molecule-1, vascular cell adhesio

216 tion of retinal tumor necrosis factor-alpha, intercellular adhesion molecule-1, vascular cell adhesio

217 reduced or absent expression of P-selectin, intercellular adhesion molecule-1, vascular cell adhesio

218 In human lung tissues, intercellular adhesion molecule-1, vascular cell adhesio

219 vascular cell adhesion molecule (VCAM)-1 and intercellular adhesion molecule-1, whereas NOR1 deficien

220 microscopy and contrast-enhanced ultrasound, intercellular adhesion molecule-1-targeted and rhodamine

221 Intercellular adhesion molecule-1-targeted and rhodamine

222 s were translatable in vivo, confirming that intercellular adhesion molecule-1-targeted and rhodamine

223 phages adhere to the beta(2) integrin ligand intercellular adhesion molecule-1.

224 senting cells was predominantly dependent on intercellular adhesion molecule-1.

225 n-6, vascular endothelial growth factor, and intercellular adhesion molecule-1.

226 complement fragments iC3b and C3d but not to intercellular adhesion molecule-1.

227 ectin, retinol-binding protein 4) or soluble intercellular adhesion molecule-1.

228 ls of plasma endothelial biomarkers (soluble intercellular adhesion molecule-1: OR, 1.58; 95% CI, 1.2

229 huTreg, or their respective porcine ligands intercellular adhesion molecule 2 (CD102) and vascular c

230 sured on choroidal-scleral flat mounts using intercellular adhesion molecule 2 immunofluorescence sta

231 riven by an endothelial-specific promoter of intercellular adhesion molecule 2.

232 ard this goal, we recently demonstrated that intercellular adhesion molecule-2 (ICAM-2) converted neu

233 and beta1, and their counterligands, such as intercellular adhesion molecule-2 and P-selectin, in bre

234 on Willebrand factor [vWF], VE-cadherin, and intercellular adhesion molecule-2), but not all (eg, VEG

235 dherin, von Willebrand factor, endoglin, and intercellular adhesion molecule-2.

236 Serum levels of E-selectin, intercellular adhesion molecule 3 matrix metalloproteina

237 eting the C-type lectin receptor DC-specific intercellular adhesion molecule 3-grabbing nonintegrin (

238 membrane receptors, dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (

239 and 2, dectin 1, and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin i

240 annose receptor- and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin-m

241 engulfed by mucosal dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin-p

242 rs, the most important being the DC-specific intercellular adhesion molecule-3 (ICAM-3)-grabbing noni

243 better interaction with DC-SIGN [DC-specific intercellular adhesion molecule-3 (ICAM-3)-grabbing noni

244 the C-type lectins, dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin

245 or downregulation of dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin

246 st Dll4, CD68, CD14, Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin

247 ans cells (LCs), and dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin

248 face lectin DC-SIGN (dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin)

249 recognition receptor dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (

250 was not mediated by dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (

251 r receptors, such as dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (

252 Dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (

253 R, efficiently bound dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (

254 the C-type lectin receptor (CLR) DC-specific intercellular adhesion molecule-3-grabbing nonintegrin (

255 We used dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin a

256 DC-SIGN (dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin)

257 ding molecules CCR5, dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin,

258 CD3, CCR5, Langerin, dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin,

259 d F(ab')2 fragments of IVIg with DC-specific intercellular adhesion molecule-3-grabbing nonintegrin.

260 repeats and discoidin I-like domains 3, and intercellular adhesion molecule 4; the first three have

261 ecule (BCAM/Lu) and ECM laminin, and between intercellular adhesion molecule-4 (ICAM-4) and endotheli

262 RBCs to endothelial cells is mediated by the intercellular adhesion molecule-4 (ICAM-4), which appear

263 rocyte adhesion receptor Landsteiner-Wiener (intercellular adhesion molecule-4).

264 Here we identify neuron-specific intercellular adhesion molecule 5 (ICAM-5/telencephalin)

265 al fibrillary acidic protein (p = 0.001) and intercellular adhesion molecule-5 (p = 0.001).

266 The telencephalon-associated intercellular adhesion molecule-5 (telencephalin; ICAM-5

267 f) ligand 2, neuron-specific enolase, S100b, intercellular adhesion molecule-5, and brain-derived neu

268 CEA functions as an intercellular adhesion molecule and is upregulated in a

269 tein and mRNA analysis demonstrated enhanced intercellular adhesion molecule and vascular cell adhesi

270 e (VCAM); 5) interleukin (IL)-6; 6) IL-8; 7) intercellular adhesion molecule; and 8) IL-10.

271 -1, Bax and caspase-3, protein expression of intercellular adhesion molecule as well as the number of

272 Soluble endothelial selectin and soluble intercellular adhesion molecule concentrations decreased

273 that AP-1 regulates the localization of the intercellular adhesion molecule E-cadherin and that loss

274 barrier alteration is prevented by reducing intercellular adhesion molecule expression and pericyte

275 duced pulmonary interleukin-6 transcription, intercellular adhesion molecule expression, neutrophil i

276 th complex I inhibition, NFKB activation and intercellular adhesion molecule expression.

277 NFAT-independent adhesion of T cells to the intercellular adhesion molecule ICAM-1, with little effe

278 t but is essential for efficient adhesion to intercellular adhesion molecule (ICAM) 1 and vascular ce

279 retained locally through constitutive LFA-1-intercellular adhesion molecule (ICAM) 1 interactions.

280 exhibiting a 70 and 50% increase in retinal intercellular adhesion molecule (ICAM)-1 expression and

281 Intercellular adhesion molecule (ICAM)-1 functions to en

282 ctivity of platelets taken from mice lacking intercellular adhesion molecule (ICAM)-1 identified a ma

283 selectin reduced their rolling velocity when intercellular adhesion molecule (ICAM)-1 was available.

284 domain, antagonized the I domain binding to intercellular adhesion molecule (ICAM)-1, complement C3

285 ng loops in vascular cell adhesion molecule, intercellular adhesion molecule (ICAM)-1, ICAM-2, ICAM-3

286 In the validation cohort concentrations of intercellular adhesion molecule (ICAM)-1, IL-8, and vasc

287 Antibody blockade of intercellular adhesion molecule (ICAM)-1, vascular cell

288 BS resulted in significant downregulation of intercellular adhesion molecule (ICAM)-1, vascular cell

289 f other genes such as interleukin (IL)-8 and intercellular adhesion molecule (ICAM)-1.

290 ascular cell adhesion molecule (VCAM)-1, and intercellular adhesion molecule (ICAM)-1.

291 found on lymphocytes, and its cognate ligand intercellular adhesion molecule (ICAM)-1.

292 Interactions between intercellular adhesion molecules (ICAMs) and their ligan

293 E(-)H(+) beta2 integrins bind intercellular adhesion molecules (ICAMs) in cis, which i

294 igen-1 (LFA-1; integrin alpha(L)beta(2)) for intercellular adhesion molecules (ICAMs) on endothelia o

295 rations in the jugular bulb, whereas soluble intercellular adhesion molecule increased significantly

296 ve activities involved CD40, CD80, CD86, and intercellular adhesion molecule interactions and require

297 Elevated serum levels of soluble-intercellular adhesion molecule, soluble-vascular cell a

298 spine apparatus, and telencephalin (TLCN, or intercellular adhesion molecule type 5), a protein assoc

299 tissue plasminogen activator, interleukin-6, intercellular adhesion molecule, vascular cell adhesion

300 complex), and the adhesion molecule soluble intercellular adhesion molecule were measured.

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