ライフサイエンスコーパス: cell adhesion molecule

1 s, most commonly in the brain, on the neural cell adhesion molecule.

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

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

4 blocking adhesion mediated by the L1 neural cell adhesion molecule.

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

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

7 ge-independent growth, are both dependent on cell adhesion molecules.

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

9 intravenously injected antibody to vascular cell adhesion molecule 1 (anti-VCAM) in the inflamed bra

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

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

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

13 ults showed that carcinoembryonic Ag-related cell adhesion molecule 1 (CEACAM-1), a molecule expresse

14 ntify the NET-associated carcinoembryonic Ag cell adhesion molecule 1 (CEACAM1) as an essential eleme

15 with absent carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) exhibited increased i

16 ion between carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) expression and malign

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

18 ed in wildtype mice, glycosylation-dependent cell adhesion molecule 1 (Glycam1), expressed 7-fold hig

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

20 ntibodies against mucosal vascular addressin cell adhesion molecule 1 (MADCAM1), which is capable of

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

22 Neural cell adhesion molecule 1 (NCAM1; CD56) is expressed in u

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

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

25 continuous detection of platelet endothelial cell adhesion molecule 1 (PECAM-1)-dependent, outside-in

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

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

28 ted to the lungs via RAGE-dependent vascular cell adhesion molecule 1 (VCAM-1) expression on lung end

29 red by binding of beta1-integrin to vascular cell adhesion molecule 1 (VCAM-1) on neurons in the infl

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

31 t induction of the pro-inflammatory vascular cell adhesion molecule 1 (VCAM1) cell-adhesion protein.

32 profile with focal upregulation of vascular cell adhesion molecule 1 (VCAM1), a protein that facilit

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

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

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

36 BD-E2 rats exhibited a reduction in vascular cell adhesion molecule 1 expression and reduced cytokine

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

38 ercellular adhesion molecule 1, and vascular cell adhesion molecule 1 expression; and (e) ELISA for c

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

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

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

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

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

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

45 l-derived von Willebrand factor and vascular cell adhesion molecule 1, sensitizes DTCs to chemotherap

46 tercellular Adhesion Molecule 1 and Vascular Cell Adhesion Molecule 1, thereby amplifying leukocyte t

47 rkers (Flk1, Tal1/Scl1, platelet endothelial cell adhesion molecule 1, vascular endothelial-cadherin,

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

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

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

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

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

53 beta-toxin (CPB) binds platelet endothelial cell adhesion molecule-1 (PECAM-1) (also known as CD31)

54 se in the expression of platelet endothelial cell adhesion molecule-1 (PECAM-1) and a decrease in the

55 se in the expression of platelet endothelial cell adhesion molecule-1 (PECAM-1) and a decrease in the

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

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

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

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

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

61 pancreatic cancer and found soluble vascular cell adhesion molecule-1 (sVCAM-1) increases in response

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

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

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

65 g-induced endothelial expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhe

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

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

68 ar adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1), are expressed.

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

70 subunit on myeloma cells stimulated vascular cell adhesion molecule-1 (VCAM1) on MSCs, leading to the

71 : 1.30 mmol/L; P = 0.021), and intercellular cell adhesion molecule-1 (WA: 153.9 ng/mL; CB: 159.4 ng/

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

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

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

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

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

77 othelial growth factor, and soluble vascular cell adhesion molecule-1 were associated with DFU healin

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

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

80 -1 increased eosinophil adhesion to vascular cell adhesion molecule-1, caused redistribution of integ

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

82 llular adhesion molecule-1, soluble vascular cell adhesion molecule-1, soluble E-Selectin, and P-Sele

83 fms-like tyrosine kinase-1, soluble vascular cell adhesion molecule-1, soluble intercellular adhesion

84 inflammation (p65, caspase 1, VCAM [vascular cell adhesion molecule-1], ICAM [intercellular adhesion

85 of endothelial absence of mucosal addressin cell-adhesion molecule-1 (MAdCAM-1), which was also coup

86 eptor mouse carcinoembryonic antigen-related cell adhesion molecule 1a (mCEACAM1a) and mediate virus

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

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

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

90 ancer carcinoembryonic antigen (CEA)-related cell adhesion molecules 5 (CEACAM5) & 1 (CEACAM1) were u

91 usly unrecognized guidance mechanism whereby cell adhesion molecules act in trans to modulate the res

92 Here, we report that that the cell adhesion molecule ALCAM (CD166) can act as an extra

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

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

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

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

97 urexophilin3 are ligands for the presynaptic cell adhesion molecule alpha-neurexin.

98 2)delta-2 is independent of the prototypical cell-adhesion molecules alpha-neurexins (alpha-Nrxns); h

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

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

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

102 e subpopulations expressing CD24, epithelial cell adhesion molecule and folate receptor alpha protein

103 s expressing the oncogenic target epithelial cell adhesion molecule and identify a panel of three nov

104 ion in the polysialylated form of the neural cell adhesion molecule and in perineuronal nets surround

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

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

107 istinct interactions are collectively called cell adhesion molecules and are divided into four major

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

109 lls found a strong positive correlation with cell adhesion molecules and IFN response pathways and a

110 Differences in cell adhesion molecules and leukocyte adhesion were abla

111 Here, we discuss how glial cell adhesion molecules and the extracellular matrix mol

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

113 ynaptic binding with neurexin, a presynaptic cell adhesion molecule, and also binds to PSD-95, althou

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

115 increased HEVs, upregulated chemokines, and cell adhesion molecules, and led to greater numbers of T

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

117 e functionalized with anti-EpCAM (epithelial cell adhesion molecule) antibodies to isolate CTCs from

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

119 Many cell adhesion molecules are present along myelinated axo

120 Genes encoding cell adhesion molecules are significantly enriched in Ee

121 tion factor of the Wnt signaling pathway and cell adhesion molecule, as a CK5 interactor, which we co

122 ein level of alpha5beta1 integrin, the major cell adhesion molecule at the surface of HeLa and MDA-MB

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

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

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

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

127 to promote the cytokine-induced inflammatory cell adhesion molecule (CAM) expression including VCAM-1

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

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

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

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

132 in vivo RNAi screen of PyN-expressed axonal cell adhesion molecules (CAMs) and select Ephs/ephrins.

133 On the other hand, up-regulation of cell adhesion molecules (CAMs) associated genes was only

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

135 derstanding the dynamical gene regulation of cell adhesion molecules (CAMs) responsible for the emerg

136 ndrocyte-axon contact is mediated by several cell adhesion molecules (CAMs) that are positioned at di

137 y impacts the synthesis of membrane-targeted cell adhesion molecules (CAMs), measured by pulsed stabl

138 ed that G protein-coupled receptors (GPCRs), cell adhesion molecules (CAMs), receptor tyrosine kinase

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

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

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

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

143 A novel electrochemical sensor for a neural cell adhesion molecule (CD56) was constructed by glycosy

144 D83, SIGLEC12, as well as the CD2 ligand and cell adhesion molecule CD58, all of which may be involve

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

146 eins of the carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family, which interact w

147 up-regulate carcinoembryonic antigenrelated cell adhesion molecules (CEACAMs) on the surface of smal

148 Cell adhesion molecule close homolog of L1 (CHL1) and th

149 euronal effector genes, such as channels and cell adhesion molecules, contribute disproportionately t

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

151 Two interacting cell adhesion molecules, Dpr11 and DIPgamma, are essenti

152 ing protein-1 (Xbp1), (ii) the Down Syndrome Cell Adhesion Molecule (Dscam) gene and iii) the embryon

153 The Down Syndrome Cell Adhesion Molecule (Dscam) gene from Drosophila is o

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

155 Down syndrome cell adhesion molecules (dscam and dscaml1) are essentia

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

157 ttern with the epithelial cell-specific cell-cell adhesion molecule E-cadherin in the dental epitheli

158 The cell adhesion molecule E-cadherin is a major component o

159 lls), we show that IFs downregulate the cell-cell adhesion molecule E-cadherin on non-tumorigenic cel

160 The endothelial cell adhesion molecule E-selectin is a key component of

161 ing on HUVEC cells by decreasing endothelial cell adhesion molecule E-Selectin production, (ii) trans

162 C with a concurrent reduction in endothelial cell adhesion molecule E-selectin, (ii) transmigration t

163 in cone-dominant species, we identified the cell-adhesion molecule ELFN2 to be pivotal for the funct

164 We found that the SAX-7/L1CAM cell adhesion molecule engages in distinct molecular mec

165 that the extracellular domain of epithelial cell adhesion molecule (EpCAM) (EpEX) significantly incr

166 d to an antibody specific for the epithelial cell adhesion molecule (EpCAM) and sorted into four zone

167 Although epithelial cell adhesion molecule (EpCAM) has previously been shown

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

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

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

171 otein 12 (AKAP12), cytokeratin 7, epithelial cell adhesion molecule (EPCAM), and carbamoyl palmitate

172 surface receptors, which included epithelial cell adhesion molecule (EpCAM), carbonic anhydrase IX (C

173 specificity for a model antigen, epithelial cell adhesion molecule (EpCAM), this study demonstrates

174 at is monovalent for both Met and epithelial cell adhesion molecule (EpCAM).

175 onstant [K(D)], 2.9 nM) and mouse epithelial cell adhesion molecule (EpCAM; K(D), 21 nM), and with [(

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

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

178 cted T cell-associated molecule (CRTAM) is a cell adhesion molecule expressed by intraepithelial T ce

179 ofascin-155 (Nfasc155) is an essential glial cell adhesion molecule expressed in paranodal septate-li

180 I classical cadherins constitute a family of cell adhesion molecules expressed in complex combinatori

181 adder cancer cells based on their Epithelial Cell Adhesion Molecule expression (>90%) and detection b

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

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

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

185 tions, L1, a brain derived neuronal specific cell adhesion molecule, has been covalently bound to the

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

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

188 mics identified the immunoglobulin family of cell adhesion molecules (IgCAMs) as direct substrates, w

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

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

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

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

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

194 the expression of intercellular and vascular cell adhesion molecules in EC, an effect that was also H

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

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

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

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

199 imited knowledge exists on the relevant cell-cell adhesion molecules involved in physiological epithe

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

201 Bidirectional signaling by cell adhesion molecules is thought to mediate synapse fo

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

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

204 Proteolytic cleavage of the cell adhesion molecule L1 (L1) in brain tissue and in cu

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 (2019) identify the cell adhesion molecule L1CAM as integral to the mechanis

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

211 ine-methacrylate) coated beads to isolate L1 cell adhesion molecule (L1CAM)-positive extracellular ve

212 Lutheran/basal cell adhesion molecule (Lu/BCAM) promotes tumor cell mig

213 on to recombinant mucosal vascular addressin cell adhesion molecule (MAdCAM-)1 in vitro as well as th

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

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

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

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

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

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

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

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

222 Since neural cell adhesion molecule (NCAM) activates FGF receptors, w

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

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

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

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

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

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

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

230 ariable inter-subject accumulation of neural cell adhesion molecule (NCAM)-positive myofibres, and an

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

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

233 We identified Neural Cell Adhesion Molecule (NCAM1) as a potential ZIKV recep

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

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

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

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

238 conserved IgCAMs (immunoglobulin superfamily cell adhesion molecules), neuroglian (Nrg) and fasciclin

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

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

241 Many mutations on X-linked cell adhesion molecule NLGN4X result in ASD or intellect

242 lso identify transcription factors (TFs) and cell-adhesion molecules not previously implicated in NC

243 n junctions in vivo, which includes neuronal cell adhesion molecule (NRCAM).

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

245 nodes of Ranvier is mediated by a number of cell adhesion molecules of the immunoglobulin superfamil

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

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

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

249 ffinity ligands specific for the endothelial cell adhesion molecules, PECAM-1 (CD31) and ICAM-1 (CD54

250 growth response (EGR3), platelet endothelial cell adhesion molecule (PECAM1) and L-selectin (SELL) we

251 of the conserved IgSF9-family trans-synaptic cell adhesion molecules, plays a novel and specific role

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

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

254 tibodies have utility for killing epithelial cell adhesion molecule-positive cells when used as a tar

255 examine this concept, we cultured epithelial cell adhesion molecule-positive reactive cholangioids (E

256 and NCAM1/2, respectively, Nrg and Fas2 are cell adhesion molecules primarily studied in the context

257 ic axonal plasma membrane domains through L1 cell-adhesion molecule protein, where it couples microtu

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

259 Synaptic cell adhesion molecules regulate signal transduction, sy

260 ic studies have strongly implicated synaptic cell adhesion molecules (sCAMs) in several such disorder

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

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

263 sion of numerous protein families, including cell-adhesion molecules, surface receptors, and their li

264 Furthermore, we identified the conserved cell adhesion molecule SYG-1/Neph as a receptor for the

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 The trans-synaptic interaction of the cell-adhesion molecules teneurins (TENs) with latrophili

268 is also observed with a loss of GlialCAM, a cell adhesion molecule that binds to ClC-2 in glia.

269 -519d in determining expression of a pivotal cell adhesion molecule that may impact risks of malignan

270 4 (NECL4, CADM4) is a Schwann cell-specific cell adhesion molecule that promotes axo-glial interacti

271 in and proline-rich receptor-1 (IGPR-1) is a cell adhesion molecule that regulates angiogenesis and e

272 codes single-pass transmembrane postsynaptic cell adhesion molecules that are important for synapse a

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

274 Neuroligins, postsynaptic cell adhesion molecules that are linked to neuropsychiat

275 Neurexins are well-characterized presynaptic cell adhesion molecules that engage multifarious postsyn

276 of muscle relied upon the same suite of cell-cell adhesion molecules that functioned in the endogenou

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

278 roligins (NLGNs) are a class of postsynaptic cell adhesion molecules that interact with presynaptic n

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

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

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

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

283 Neurexins are presynaptic, cell-adhesion molecules that specify the functional prop

284 n, intercellular adhesion molecule, vascular cell adhesion molecule, thrombomodulin) and inflammatory

285 n, intercellular adhesion molecule, vascular cell adhesion molecule, thrombomodulin, endocan, C-react

286 vascular endothelial growth factor, vascular cell adhesion molecule, thrombomodulin, endocan, interle

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

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

289 This study demonstrates that cell adhesion molecule transmembrane and immunoglobulin

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

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

292 es lipopolysaccharide (LPS)-induced vascular cell adhesion molecule (VCAM) protein levels by ~50%, wh

293 hotoxin beta receptor (LTbetaR) and vascular cell adhesion molecule (VCAM), but not intercellular adh

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

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

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

297 Membrane-anchored PrP(C) and neural cell adhesion molecule were not required for S-PrP-initi

298 otein V), GRN (granulin), and MCAM (melanoma cell adhesion molecule) were associated with PLT, while

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

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