ライフサイエンスコーパス: cell adhesion molecule

1 ted Ag 1 and lacked expression of epithelial cell adhesion molecule.

2 hibit increased surface expression of the L1 cell adhesion molecule.

3 e ILT3 ligand is a CD166/activated leukocyte cell adhesion molecule.

4 e-gated Nav and Kv7 channels associated with cell adhesion molecules.

5 interactions with platelets and endothelial cell adhesion molecules.

6 en when TM and EPCR are anchored to distinct cell adhesion molecules.

7 flammation, matrix-receptor interaction, and cell adhesion molecules.

8 amplified by chemical signaling initiated by cell adhesion molecules.

9 cretion of major proinflammatory factors and cell adhesion molecules.

10 rs of endothelial activation such as soluble cell adhesion molecules.

11 ssociates with membrane complexes comprising cell adhesion molecules.

12 y interactions between pre- and postsynaptic cell-adhesion molecules.

13 ] vs. 1.66 [1.22-2.63] p < 0.0001), vascular cell adhesion molecule 1 (539 [451-621] vs. 402 [342-487

14 Human carcinoembryonic antigen-related cell adhesion molecule 1 (C?/Au: EACAM1) is a cell-surfa

15 ns between body mass index and two loci near cell adhesion molecule 1 (CADM1) and cell adhesion molec

16 says to establish that the tumour suppressor Cell adhesion molecule 1 (CADM1) inhibits SqCC prolifera

17 neutralization of stem cell factor (SCF) or cell adhesion molecule 1 (CADM1).

18 lar adhesion molecule 2 (CD102) and vascular cell adhesion molecule 1 (CD106).

19 A1, we detected reduced platelet endothelial cell adhesion molecule 1 (CD31) and increased endothelia

20 Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) is expressed at high

21 Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) promotes hepatic insu

22 a heterodimer with carcinoembryonic antigen cell adhesion molecule 1 (CEACAM1), another well-known m

23 , and ultimately for promoting intracellular cell adhesion molecule 1 (ICAM-1) binding.

24 sion by T cells, chemokine and intracellular cell adhesion molecule 1 (ICAM-1) expression in the brai

25 ulates the lateral mobility of intracellular cell adhesion molecule 1 (ICAM-1), but not MHCII.

26 pendent on Schwann cell expression of neural cell adhesion molecule 1 (NCAM1) and ultimately promoted

27 the endothelial activation markers vascular cell adhesion molecule 1 (P < .001 for both) and angiopo

28 Platelet Endothelial Cell Adhesion Molecule 1 (PECAM-1) is a major component

29 ntegrins and recognizes platelet endothelial cell adhesion molecule 1 (PECAM-1), suggesting a role in

30 zed the synapse-organizing proteins Synaptic Cell Adhesion Molecule 1 (SynCAM 1) and EphB2.

31 for NCAM, neuropilin-2 (NRP-2), and synaptic cell adhesion molecule 1 (SynCAM 1) for polysialylation

32 The levels of soluble vascular cell adhesion molecule 1 (VCAM-1) and osteoprotegerin we

33 Here, we show that red pulp vascular cell adhesion molecule 1 (VCAM-1)(+) macrophages are ess

34 pression of an inflammatory marker, vascular cell adhesion molecule 1 (VCAM-1), in atherosclerotic pl

35 llular adhesion molecule 1 (ICAM-1)/vascular cell adhesion molecule 1 (VCAM-1)-mediated adhesion of b

36 ellular adhesion molecule 1 (ICAM1)/vascular cell adhesion molecule 1 (VCAM1), whose expression was a

37 kines, and cell adhesion molecules (vascular cell adhesion molecule 1 [VCAM-1] and intracellular adhe

38 ibitor of metalloproteinases 1; and vascular cell adhesion molecule 1 [VCAM-1]) were measured by usin

39 k of vessels expressing platelet/endothelial cell adhesion molecule 1 and vascular endothelial growth

40 function blocking anti-platelet endothelial cell adhesion molecule 1 antibody, depolymerizing microt

41 s vascular ligand mucosal vascular addressin cell adhesion molecule 1 are proving the value of lympho

42 e posttranscriptional regulation of vascular cell adhesion molecule 1 expression and a reduced number

43 ted with a marked reduction in lung vascular cell adhesion molecule 1 expression and production of se

44 dhesion molecule 1, and platelet endothelial cell adhesion molecule 1 expression when stimulated with

45 cells; IL-4; IL-5; eosinophils, and vascular cell adhesion molecule 1 in the large airways and bronch

46 ocyte chemoattractant protein-1 and vascular cell adhesion molecule 1 in wire-injured carotid arterie

47 lar adhesion molecule 1 and soluble vascular cell adhesion molecule 1 were reduced after whey protein

48 tracellular adhesion molecule 1 and vascular cell adhesion molecule 1) genes involved in myeloid cell

49 of CEACAM1 (carcinoembryonic antigen-related cell adhesion molecule 1), a transmembrane glycoprotein

50 Vascular cell adhesion molecule 1, an adhesion molecule that medi

51 mor necrosis factor alpha receptor, vascular cell adhesion molecule 1, and matrix metalloproteinase 2

52 rkers (CD34, endomucin, platelet endothelial cell adhesion molecule 1, and plasmalemmal vesicle-assoc

53 inished inflammation (expression of vascular cell adhesion molecule 1, plaque macrophage content) and

54 g with soluble and immobilized intercellular cell adhesion molecule 1.

55 lial activation, angiopoietin 2 and vascular cell adhesion molecule 1.

56 for the vascular marker platelet endothelial cell adhesion molecule 1.

57 ed monocyte adhesion by attenuating vascular cell adhesion molecule -1 and monocyte chemoattractant p

58 adhesion molecule mucosal vascular addressin cell adhesion molecule-1 (MAdCAM-1) and that RA increase

59 promotes cell adherence to mucosal addressin cell adhesion molecule-1 (MAdCAM-1) expressed by vascula

60 tibody that binds to human mucosal addressin cell adhesion molecule-1 (MAdCAM-1) to selectively reduc

61 cells, colocalizes with platelet/endothelial cell adhesion molecule-1 (PECAM) to surround leukocytes

62 ion molecules including Platelet-Endothelial Cell Adhesion Molecule-1 (PECAM-1 or CD31) improves drug

63 Platelet endothelial cell adhesion molecule-1 (PECAM-1) is a 130-kDa member o

64 cule (MCAM)/MUC18, CD31/platelet endothelial cell adhesion molecule-1 (PECAM-1), CD144/VE-cadherin, a

65 One CAM member, platelet-endothelial-cell adhesion molecule-1 (PECAM-1), plays an important r

66 ion of the shear sensor platelet endothelial cell adhesion molecule-1 (PECAM-1).

67 urface targets like the Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1, a highly expressed en

68 r adhesion molecule-1 (sICAM-1) and vascular cell adhesion molecule-1 (sVCAM-1) were higher following

69 p II: 0.14 (0.20) mug/mL, P = .02); vascular cell adhesion molecule-1 (VCAM-1) (Group I: 0.34 (0.67)

70 an PDEs of the endothelial proteins vascular cell adhesion molecule-1 (VCAM-1) and endothelial nitric

71 ing that controls expression of the vascular cell adhesion molecule-1 (VCAM-1) and monocyte adhesion

72 enesis, but increased expression of vascular cell adhesion molecule-1 (VCAM-1) in primary culture of

73 lular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin, resul

74 subsequent induction of endothelial vascular cell adhesion molecule-1 (VCAM-1), which is required for

75 ar adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1).

76 and increased plasma levels of intercellular cell adhesion molecule-1 and monocyte chemoattractant pr

77 and plasma adhesion molecules, intercellular cell adhesion molecule-1 and monocyte chemoattractant pr

78 ination by increasing expression of vascular cell adhesion molecule-1 and the transcytosis protein Ca

79 Furthermore, vascular cell adhesion molecule-1 expression in both mouse and hu

80 was associated with an increase in vascular cell adhesion molecule-1 expression, which itself was re

81 d with beta-blocker showed enhanced vascular cell adhesion molecule-1 expression.

82 tores the expression of platelet endothelial cell adhesion molecule-1 in glomerular endothelial cells

83 l adhesion molecules E-selectin and vascular cell adhesion molecule-1 in the microvasculature of kidn

84 Platelet-endothelial cell adhesion molecule-1 is a transmembrane protein conn

85 , neuron-specific enolase, and intracellular cell adhesion molecule-1 levels did not differ between n

86 derived microparticles, platelet-endothelial cell adhesion molecule-1 lung protein content, and immun

87 me-controlled ventilation increased vascular cell adhesion molecule-1 messenger RNA expression (volum

88 onic PTSD had a greater increase in vascular cell adhesion molecule-1 over time (B = 0.003, p < .05).

89 cles and a reduction of platelet-endothelial cell adhesion molecule-1 protein levels in the high-tida

90 thelial activation markers (soluble vascular cell adhesion molecule-1) decreased but remained elevate

91 tercellular adhesion molecule-1 and vascular cell adhesion molecule-1) in 524 middle-aged women in th

92 Tumour necrosis factor alpha, vascular cell adhesion molecule-1, 8-isoprostane, leptin, circula

93 intercellular adhesion molecule-1, vascular cell adhesion molecule-1, and E-selectin expressions are

94 igh-mobility group protein B1, intracellular cell adhesion molecule-1, and leptin, as well as previou

95 -1 increased eosinophil adhesion to vascular cell adhesion molecule-1, caused redistribution of integ

96 necrosis factor receptor-1, soluble vascular cell adhesion molecule-1, granulocyte colony-stimulating

97 asing the expression of E-selectin, vascular cell adhesion molecule-1, intercellular adhesion molecul

98 Plasminogen activator inhibitor 1, vascular cell adhesion molecule-1, intracellular adhesion molecul

99 oparticles positive for platelet-endothelial cell adhesion molecule-1, which could serve as potential

100 1 and loss of binding to its ligand vascular cell adhesion molecule-1.

101 nder and education) in an intron of the gene cell adhesion molecule 2 (CADM2) for performance on the

102 ci near cell adhesion molecule 1 (CADM1) and cell adhesion molecule 2 (CADM2), which encode membrane

103 Changes in expression of the neural cell adhesion molecule 2 (NCAM2) have been proposed to c

104 e targeting carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) for tumor delivery of

105 ith catecholamines, carcinoembryonic antigen cell adhesion molecule 8 (CEACAM8), and IFN-gamma caused

106 sitively associated with activated leukocyte cell adhesion molecule (ALCAM) and C-reactive protein (C

107 Activated leukocyte cell adhesion molecule (ALCAM) is a cell adhesion molecu

108 Activated leukocyte cell adhesion molecule (ALCAM) is expressed on various c

109 Activated leukocyte cell adhesion molecule (ALCAM) mediates cell aggregation

110 included networks for calcium signaling and cell adhesion molecules, among others.

111 nin is caused by its dual functionality as a cell adhesion molecule and a signaling molecule.

112 ody weight), caused low levels of epithelial cell adhesion molecule and cytokeratin 19 gene messenger

113 vate, its high-affinity state binds vascular cell adhesion molecule and fibronectin 100- to 1,000-fol

114 ing our attention on two markers, epithelial cell adhesion molecule and leucine-rich repeat-containin

115 -expression of the melanoma markers melanoma cell adhesion molecule and melanoma-associated chondroit

116 n silico network model of interactions among cell adhesion molecules and a network-focused microarray

117 h could be because of impaired expression of cell adhesion molecules and an altered cell surface glyc

118 ble TXA2 metabolite) and PGF2alpha , soluble cell adhesion molecules and blood pressure were measured

119 te adhesion is mediated mainly by selectins, cell adhesion molecules and chemokines induced by pro-in

120 icine includes peptidases and other enzymes, cell adhesion molecules and integrins, localized in diff

121 cores, and proinflammatory VCAM-1 (vascular cell adhesion molecule) and MCP-1 (monocyte chemotactic

122 activation and circulating soluble vascular cell adhesion molecule), and a significant improvement i

123 action with CD166/ALCAM (activated leukocyte cell adhesion molecule), and physically associates with

124 class I human leukocyte antigen, epithelial cell adhesion molecule, and cytokeratin-19.

125 radically different role for this well-known cell adhesion molecule, and propose that Fas2-mediated i

126 determining region Y)-box 9, and epithelial cell adhesion molecule; and enriched for transcripts of

127 in superfamily molecules such as the Aplysia cell adhesion molecule (apCAM) leads to actin filament a

128 cantilever that was modified with an Aplysia cell adhesion molecule (apCAM)-coated microbead.

129 Their cell adhesion molecules are cadherins: type 1 cadherins

130 Genes encoding cell adhesion molecules are significantly enriched in Ee

131 However, many other postsynaptic cell-adhesion molecules are known and the relative contr

132 ll expression profiles of candidate synaptic cell adhesion molecules, are not known.

133 gated sodium channels (VGSCs) aggregate with cell adhesion molecules at discrete subcellular location

134 E-cadherin is a cell adhesion molecule best known for its function in su

135 culating cells, especially by overexpressing cell adhesion molecules, but also by other as yet unknow

136 f neurexin isoforms and other trans-synaptic cell-adhesion molecules by microfluidics-based RT-PCR.

137 Cell adhesion molecule cadherins play important roles in

138 approximately 20-30%; P < 0.05) decreases in cell adhesion molecule (Cadm)4 and p39 mRNAs, as well as

139 Contactin-4 (CNTN4) is a complex cell adhesion molecule (CAM) localized at neuronal membr

140 on depends on Neuroligin 2 (NL2), a synaptic cell adhesion molecule (CAM).

141 d by a 24-48 hour-long response of increased cell adhesion molecules (CAM), trophic and anti-inflamma

142 and pathogen infection is mainly mediated by cell adhesion molecules (CAM).

143 Cell adhesion molecules (CAMs) play a central role in th

144 are maintained by membrane receptors called cell adhesion molecules (CAMs), which are expressed on c

145 growth cone positioning is consolidated via cell-adhesion molecule Capricious in R8 axons.

146 ut mice lacking both NF186 and the paranodal cell adhesion molecule Caspr, demonstrating that a paran

147 , we report evidence of a major role for the cell adhesion molecule CD166, which we discovered to be

148 Our results demonstrate that the cell adhesion molecule CD34 was widely expressed by the

149 bers of the carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family as receptors of H

150 n of gene expression for carcinoembryonic Ag cell adhesion molecule (CEACAM) family members in the br

151 uring tumorigenesis along with expression of cell adhesion molecule CEACAM1.

152 Carcinoembryonic antigen-related cell adhesion molecules (CEACAMs) comprise a large famil

153 s (rs12764057, rs10822974, rs7903491) in the cell-adhesion molecule CTNNA3 were significant in the co

154 In vivo silencing of endothelial cell adhesion molecules curbed post-MI monocyte recruitm

155 in levels of cytokines [activated leukocyte cell adhesion molecule, CXCL-16, and ErbB3] to those in

156 In brain, signaling mediated by cell adhesion molecules defines the identity and functio

157 Down syndrome cell adhesion molecule (Dscam) is expressed by mouse RGC

158 Increased expression of Down Syndrome Cell Adhesion Molecule (Dscam) is implicated in the path

159 f-function mouse allele of the Down syndrome cell adhesion molecule (Dscam) to complement loss-of-fun

160 The Down syndrome cell-adhesion molecule (Dscam) confines these anatomical

161 on-induced protein expression of endothelial cell adhesion molecules E-selectin and vascular cell adh

162 CR4(+) with reduced expression of epithelial cell adhesion molecule (EpCAM(-)), which also shows the

163 xpression of PRC2-repressed genes epithelial cell adhesion molecule (EpCAM) and pluripotency genes.

164 of alpha-amanitin-conjugated anti-epithelial cell adhesion molecule (EpCAM) antibody lead to complete

165 Overexpression of epithelial cell adhesion molecule (EpCAM) has been implicated in ad

166 The epithelial cell adhesion molecule (EpCAM) is closely correlated wit

167 Epithelial cell adhesion molecule (EpCAM) is expressed at the basol

168 response to contact sensitizers, epithelial cell adhesion molecule (EpCAM) on LCs promotes LC dendri

169 ancer cell death by cross-linking epithelial cell adhesion molecule (EpCAM) on tumor cells with a clu

170 ed with antibodies against either epithelial cell adhesion molecule (EpCAM) or epidermal growth facto

171 ds coated with antibodies against epithelial-cell adhesion molecule (EpCAM) via magnetic-activated ce

172 mens were stained with trichrome, epithelial cell adhesion molecule (EpCAM), K19, CD34, glutamine syn

173 1beta, HNF3beta, HNF4alpha, HNF6, Epithelial cell adhesion molecule (EpCAM), Leucine-rich repeated-co

174 ssion of several genes, including epithelial cell adhesion molecule (EpCAM).

175 the cell surface antigen known as epithelial cell adhesion molecule (EpCAM).

176 endothelial MPs, epithelial MPs (epithelial cell adhesion molecule [EpCAM](+)MPs, E-cadherin(+)MPs),

177 ), identifying cancer stem cells (epithelial cell adhesion molecule [EpCAM], neural cell adhesion mol

178 lustered delta-protocadherins are homophilic cell adhesion molecules essential for the development of

179 gether, we have identified TMIGD1 as a novel cell adhesion molecule expressed in kidney epithelial ce

180 bers of the carcinoembryonic antigen-related cell adhesion molecule family (CEACAMs) as host cell rec

181 eukocyte cell adhesion molecule (ALCAM) is a cell adhesion molecule found on blood-brain barrier endo

182 Neuroligins are postsynaptic cell-adhesion molecules genetically linked to autism.

183 Human epithelial cell adhesion molecule (HEPCAM) is a tumor-associated an

184 ough Pcdh19 is known to be a homophilic cell-cell adhesion molecule, how its mutations bring about fe

185 6 substrate MMP14 (MT1-MMP) as well as L1CAM cell adhesion molecule, identified here as a novel MMP16

186 The Ig-like cell adhesion molecule (IgCAM) BT-IgSF (brain- and testi

187 known as OB cadherin or CDH11) is a cell-to-cell adhesion molecule implicated in many biological fun

188 Neuroligins are postsynaptic cell-adhesion molecules implicated in autism and other n

189 alpha- and beta-neurexins are presynaptic cell-adhesion molecules implicated in autism and schizop

190 tores the expression of platelet endothelial cell adhesion molecule in glomerular endothelial cells a

191 related cytokines, eosinophils, and vascular cell adhesion molecule in the bronchopulmonary LNs and l

192 ABSTRACT: N-cadherin is the major cell-cell adhesion molecule in vascular smooth muscle cells (

193 between the nucleoskeleton, cytoskeleton and cell adhesion molecules in cells expressing the mutant p

194 terized; pemphigus antigens are desmogleins (cell adhesion molecules in desmosomes), and pemphigoid a

195 on; it also lowered the expression of cancer cell adhesion molecules in ECs by decreasing NF-kappaB s

196 tivated astrocytes, microglia, and increased cell adhesion molecules in the vasculature.

197 and adenovirus receptor (CAR), a single-pass cell adhesion molecule, in the adult brain.

198 Targeting nanocarriers (NC) to endothelial cell adhesion molecules including Platelet-Endothelial C

199 ies directed against several region-specific cell adhesion molecules, including neurofascin, contacti

200 sed surface expression of several sialylated cell adhesion molecules, including the known megakaryocy

201 group of glycophosphatidylinositol-anchored cell adhesion molecules involved in the wiring of the ne

202 we show that Cadherin-6 (Cdh6), a homophilic cell adhesion molecule, is a reliable marker of ChCs and

203 Neurexin 1 (NRXN1), a presynaptic cell adhesion molecule, is implicated in several neurode

204 el endothelium by reducing expression of the cell adhesion molecules ITGA5 and ALCAM.

205 Two proteins, the neural cell adhesion molecule L1 and dipeptidyl peptidase 4, we

206 ntially relevant to skin homeostasis: neural cell adhesion molecule L1 and dipeptidyl peptidase 4.

207 The cell adhesion molecule L1 and the extracellular matrix p

208 ficking of multiple receptors, including the cell adhesion molecule L1/NgCAM, the neurotransmitter re

209 enriched with clonal mutations involving L1 cell adhesion molecule (L1CAM) and integrin signaling pa

210 by negative emotional arousal, and of the L1 cell adhesion molecule (L1CAM) interactions gene set wit

211 ssociated with cell adhesion, among which L1 cell adhesion molecule (L1CAM) was significantly higher

212 consistent with the C. elegans divergent L1 cell adhesion molecule LAD-2 acting as a non-canonical e

213 ed by tumor blood vessels, of which melanoma cell adhesion molecule (MCAM) and its extracellular matr

214 We further identify the melanoma cell adhesion molecule (MCAM) as a novel KDM3A target ge

215 5a promotes depalmitoylation of the melanoma cell adhesion molecule (MCAM) at cysteine 590.

216 We propose that melanoma cell adhesion molecule (MCAM) is a surface marker and ad

217 chemical assessments indicated that melanoma cell adhesion molecule (MCAM) was a major Gal-1 ligand o

218 cell membrane glycoproteins, CD146/melanoma cell adhesion molecule (MCAM)/MUC18, CD31/platelet endot

219 (SOX9); integrin, alpha 6 (ITGA6); melanoma cell adhesion molecule (MCAM); phosphatidylinositol glyc

220 ults provide novel mechanistic insights into cell adhesion molecule-mediated axon-axon interactions t

221 Our results identify cell-adhesion molecule-mediated inhibition as a regulato

222 ion of several membrane proteins: ankyrin-R, cell adhesion molecules, metabotropic glutamate receptor

223 oscopy, we determined that moDCs express the cell adhesion molecule mucosal vascular addressin cell a

224 during CIL requires the participation of the cell adhesion molecule N-cadherin, which starts to be ex

225 A) and its major protein carrier, the neural cell adhesion molecule NCAM, play important roles in man

226 Prominent family members are the neural cell adhesion molecules NCAM and L1, which were the firs

227 The neural cell adhesion molecule (NCAM) and the receptor tyrosine

228 of PrP(C) protein interactors, the neuronal cell adhesion molecule (NCAM) has been studied in vivo,

229 The neural cell adhesion molecule (NCAM) is the major carrier of po

230 acid is a glycan modification of the neural cell adhesion molecule (NCAM) produced by the polysialyl

231 ic region (PBR) that are required for neural cell adhesion molecule (NCAM) recognition and subsequent

232 As a modification of the neural cell adhesion molecule (NCAM), polySia is produced by th

233 dies to these targets, including CD56/neural cell adhesion molecule (NCAM), promoted phagocytosis in

234 charged glycan mainly attached to the neural cell adhesion molecule (NCAM).

235 ation of polysialic acid (polySia) on neural cell adhesion molecules (NCAM).

236 elial cell adhesion molecule [EpCAM], neural cell adhesion molecule [NCAM], epithelial growth factor

237 is is the first demonstration of a bona fide cell adhesion molecule, NECL4, regulating choline homeos

238 We previously showed that the cell adhesion molecule Nectin-4 is overexpressed in ovar

239 he NRXN1 gene, which encodes the presynaptic cell-adhesion molecule neurexin-1, were repeatedly assoc

240 rm tripartite complexes with the presynaptic cell-adhesion molecules neurexins or 'deleted-in-colorec

241 1 as a trans-synaptic binding partner of the cell adhesion molecule neurofascin-186 (NF186) expressed

242 immunostaining with an antibody against the cell adhesion molecule neuroglian reveals the same larva

243 hat conditional deletion of the postsynaptic cell adhesion molecule neuroligin-3 in parvalbumin inter

244 r molecular families: transcription factors, cell adhesion molecules, neuropeptides, and calcium bind

245 cules [neurofascin-186, neuron glial-related cell adhesion molecule (NrCAM)] can arrange in a more co

246 f cancer-related death, and it involves cell-cell adhesion molecules of the cadherin family.

247 mice of neuroligin-2 (Nlgn2), a postsynaptic cell-adhesion molecule of inhibitory synapses linked to

248 gnetically based on expression of epithelial cell adhesion molecules; only those with a proper morpho

249 s such as surface antigens (e.g., epithelial cell adhesion molecule or EpCAM) or size to separate the

250 evel and suggest that expression of synaptic cell-adhesion molecules overlaps with other key features

251 Thus, SOD conjugated with antibodies to cell adhesion molecule PECAM (Ab/SOD) inhibits pro-infla

252 to adjacent epitopes of platelet endothelial cell adhesion molecule (PECAM)-1 stimulate each other's

253 lin receptor (pIgR) and platelet endothelial cell adhesion molecule (PECAM-1).

254 ogen; decreased total cathepsin-L1, vascular cell adhesion molecule, periostin, and neutrophil gelati

255 or genes (Cd133, Cd24, Nanog, and epithelial cell adhesion molecule), PMN infiltration, and clinical

256 esults together with those related to neural cell adhesion molecule polysialylation establish a parad

257 highly specific capture of EpCAM (epithelial cell adhesion molecule) positive CTCs from blood.

258 ontrolled via secreted signaling factors and cell adhesion molecules provided from local niche struct

259 The polysialylated form of the neural cell adhesion molecule (PSA-NCAM) functions broadly, ser

260 Synaptic cell adhesion molecules regulate signal transduction, sy

261 hypodermal cells in a pattern similar to the cell adhesion molecule SAX-7/L1CAM.

262 Gliomedin interacts with neuronal cell adhesion molecules, such as neurofascin, but the st

263 ptic dimerization, similar to other synaptic cell adhesion molecules, such as Neuroligin/Neurexin.

264 interactions that is presumably mediated by cell adhesion molecules suggests that there exists a log

265 emoattractant protein-1, soluble endothelial cell adhesion molecule, symmetrical dimethylarginine, as

266 ve optogenetic ablation of ACs marked by the cell-adhesion molecule Teneurin-3 (Tenm3) and pharmacolo

267 -519d in determining expression of a pivotal cell adhesion molecule that may impact risks of malignan

268 4 (NECL4, CADM4) is a Schwann cell-specific cell adhesion molecule that promotes axo-glial interacti

269 L-selectin is a cell adhesion molecule that tethers free-flowing leukocy

270 erins are a superfamily of calcium-dependent cell adhesion molecules that are involved in brain devel

271 Neurexins (Nrxns) are essential synaptic cell adhesion molecules that are involved in synaptic tr

272 Nectins are cell adhesion molecules that are widely expressed in hum

273 ression of important chemokine receptors and cell adhesion molecules that control the interaction of

274 Neuroligins (NLGNs) are postsynaptic cell adhesion molecules that interact trans-synaptically

275 ns are evolutionarily conserved postsynaptic cell adhesion molecules that interact with presynaptic n

276 lustering is thought to depend on two axonal cell adhesion molecules that mediate interactions betwee

277 he vertebrate Dscams (DSCAM and DSCAML1) are cell adhesion molecules that support the development of

278 Neuroligins are postsynaptic cell-adhesion molecules that bind presynaptic neurexins

279 Neuroligins are postsynaptic cell-adhesion molecules that bind to presynaptic neurexi

280 Neuroligins are postsynaptic cell-adhesion molecules that bind to presynaptic neurexi

281 Neuroligins are postsynaptic cell-adhesion molecules that contribute to synapse speci

282 in which the folate receptor interacts with cell adhesion molecules, thus regulating the apical cell

283 Multicellular organisms rely on cell adhesion molecules to coordinate cell-cell interact

284 tors to the learning rate and linking neural cell adhesion molecules to memory maintenance.

285 components, such as extracellular matrix and cell adhesion molecules, to mechanosensitive intracellul

286 lutamatergic synapse-inducing (synaptogenic) cell adhesion molecule trans-interacting with presynapti

287 of approximately 40 gene families, including cell-adhesion molecules, transmitter-modulator receptors

288 a interferon (IFN-alpha), key cytokines, and cell adhesion molecules (vascular cell adhesion molecule

289 ular adhesion molecule (ICAM) 1 and vascular cell adhesion molecule (VCAM) 1 and for proper trafficki

290 showed by the reduced expression of vascular cell adhesion molecule (VCAM)-1 in human cultured endoth

291 mor necrosis factor (TNF)-alpha; 4) vascular cell adhesion molecule (VCAM); 5) interleukin (IL)-6; 6)

292 monstrate that spatial variation in vascular cell adhesion molecule (VCAM-1) expression correlates wi

293 ed expression levels of E-selectin, vascular cell adhesion molecule (VCAM-1), and intercellular adhes

294 proteins (fibrinogen, haptoglobin and CRP), cell adhesion molecules (VCAM-1), endothelial growth fac

295 glycosylphosphatidylinositol-anchored neural cell adhesion molecules were identified and validated as

296 s, beta subunits play nonconducting roles as cell adhesion molecules, which allow them to function in

297 ve and maintain photoreceptor diversity, and cell adhesion molecules, which may mediate spatial patte

298 duced target genes encode diverse epithelial cell adhesion molecules, while mesenchymal genes involve

299 alpha- and beta-neurexins are presynaptic cell-adhesion molecules whose general importance for syn

300 expressed during these stages, including the cell adhesion molecule with homology to L1 (Chl1).