ライフサイエンスコーパス: adhesion molecule

1 tivity, and also functions as a receptor and adhesion molecule.

2 3 ligand is a CD166/activated leukocyte cell adhesion molecule.

3 ed Nav and Kv7 channels associated with cell adhesion molecules.

4 an chains and growth factors, chemokines and adhesion molecules.

5 transcription of cytokines, chemokines, and adhesion molecules.

6 eractions between pre- and postsynaptic cell-adhesion molecules.

7 lated with reduced microglia and endothelial adhesion molecules.

8 PMN migration by affecting the expression of adhesion molecules.

9 -regulation of proinflammatory cytokines and adhesion molecules.

10 tween body mass index and two loci near cell adhesion molecule 1 (CADM1) and cell adhesion molecule 2

11 e detected reduced platelet endothelial cell adhesion molecule 1 (CD31) and increased endothelial-to-

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

13 We find that intercellular adhesion molecule 1 (ICAM-1) and ICAM-2 on B cells are e

14 /moesin (ERM) phosphorylation, intercellular adhesion molecule 1 (ICAM-1) clustering, and monocyte fi

15 by T cells, chemokine and intracellular cell adhesion molecule 1 (ICAM-1) expression in the brain, an

16 dhesion molecule (VCAM-1), and intercellular adhesion molecule 1 (ICAM-1) on endothelial cells.

17 to several receptors, of which intercellular adhesion molecule 1 (ICAM-1) upregulation in brain micro

18 PfEMP1 proteins interacts with intercellular adhesion molecule 1 (ICAM-1), allowing us to predict bin

19 interleukin 1beta (IL-1beta), intracellular adhesion molecule 1 (ICAM-1), and nitric oxide synthase

20 nly 1 replication set included intercellular adhesion molecule 1 (ICAM-1), anti-LG3, aminopeptidase N

21 y alterations, and crawling on intercellular adhesion molecule 1 (ICAM-1)-expressing cells.

22 creased expression of IFNG and intercellular adhesion molecule 1 (ICAM1) and induced T-cell aggregati

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

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

25 ompensation, and soluble serum intercellular adhesion molecule 1 (sICAM-1) MFI.

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

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

28 ion of an inflammatory marker, vascular cell adhesion molecule 1 (VCAM-1), in atherosclerotic plaques

29 hesion molecule 1 [VCAM-1] and intracellular adhesion molecule 1 [ICAM-1]).

30 , and cell adhesion molecules (vascular cell adhesion molecule 1 [VCAM-1] and intracellular adhesion

31 r of metalloproteinases 1; and vascular cell adhesion molecule 1 [VCAM-1]) were measured by using enz

32 Soluble intercellular adhesion molecule 1 and soluble vascular cell adhesion m

33 and Cxcl10) and cell-adhesion (intracellular adhesion molecule 1 and vascular cell adhesion molecule

34 vessels expressing platelet/endothelial cell adhesion molecule 1 and vascular endothelial growth fact

35 on molecule 1, and platelet endothelial cell adhesion molecule 1 expression when stimulated with Aa-L

36 ased endothelial inflammation (intercellular adhesion molecule 1 expression) and increased endothelia

37 ed with diastolic function and intercellular adhesion molecule 1 expression.

38 chemoattractant protein-1 and vascular cell adhesion molecule 1 in wire-injured carotid arteries.

39 function-associated antigen 1-intercellular adhesion molecule 1 interaction, reduced T-cell producti

40 r-resistant bond clusters with intracellular adhesion molecule 1 on inflamed endothelium.

41 dhesion molecule 1 and soluble vascular cell adhesion molecule 1 were reduced after whey protein cons

42 ociated antigen 1) for ICAM-1 (intercellular adhesion molecule 1) but significantly lower than that o

43 llular adhesion molecule 1 and vascular cell adhesion molecule 1) genes involved in myeloid cell recr

44 ACAM1 (carcinoembryonic antigen-related cell adhesion molecule 1), a transmembrane glycoprotein that

45 th endothelial alphavbeta3 and intercellular adhesion molecule 1, and (3) a stimulatory role for thro

46 , adiponectin, leptin, soluble intercellular adhesion molecule 1, and E-selectin all fell short of si

47 ecrosis factor alpha receptor, vascular cell adhesion molecule 1, and matrix metalloproteinase 2, wer

48 (CD34, endomucin, platelet endothelial cell adhesion molecule 1, and plasmalemmal vesicle-associated

49 ased interleukin (IL)-6, IL-8, intercellular adhesion molecule 1, and platelet endothelial cell adhes

50 h soluble and immobilized intercellular cell adhesion molecule 1.

51 he vascular marker platelet endothelial cell adhesion molecule 1.

52 1 and beta2; thrombospondin 2; intercellular adhesion molecule 1; interleukin 6 [IL-6]; stromal cell-

53 or II (B = 0.07, p < .01), and intercellular adhesion molecule-1 (B = 0.04, p < .05) levels.

54 factor-kappa B (NF-kappaB) and intercellular adhesion molecule-1 (ICAM) (P < 0.001, respectively) and

55 concomitant with reduction of intercellular adhesion molecule-1 (ICAM-1) and diminishing the enzymat

56 ese cells through reduction of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion

57 ntify mechanisms through which intercellular adhesion molecule-1 (ICAM-1) augments the adhesive and f

58 We have previously shown that intercellular adhesion molecule-1 (ICAM-1) expressed by endothelial ce

59 Intercellular adhesion molecule-1 (ICAM-1) mediates the firm adhesion

60 man endothelial proteins CD36, intercellular adhesion molecule-1 (ICAM-1), and endothelial protein C

61 lial mechanosensitive receptor intercellular adhesion molecule-1 (ICAM-1).

62 y that binds to human mucosal addressin cell adhesion molecule-1 (MAdCAM-1) to selectively reduce lym

63 (MCAM)/MUC18, CD31/platelet endothelial cell adhesion molecule-1 (PECAM-1), CD144/VE-cadherin, and CD

64 One CAM member, platelet-endothelial-cell adhesion molecule-1 (PECAM-1), plays an important role i

65 f the shear sensor platelet endothelial cell adhesion molecule-1 (PECAM-1).

66 (CRP), serum amyloid A (SAA), intercellular adhesion molecule-1 (sICAM-1) and vascular cell adhesion

67 esion molecule-1 (sICAM-1) and vascular cell adhesion molecule-1 (sVCAM-1) were higher following the

68 0.14 (0.20) mug/mL, P = .02); vascular cell adhesion molecule-1 (VCAM-1) (Group I: 0.34 (0.67) ng/mL

69 Es of the endothelial proteins vascular cell adhesion molecule-1 (VCAM-1) and endothelial nitric oxid

70 s, but increased expression of vascular cell adhesion molecule-1 (VCAM-1) in primary culture of tumou

71 hesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1).

72 Clinical risk factors, soluble intercellular adhesion molecule-1 and endocan (both forms) were not as

73 ndothelial biomarkers (soluble intercellular adhesion molecule-1 and endocan [full-length and cleaved

74 his required the expression of intracellular adhesion molecule-1 and stabilin-1 and was facilitated b

75 on by increasing expression of vascular cell adhesion molecule-1 and the transcytosis protein Caveoli

76 he metastasis-related proteins intercellular adhesion molecule-1 and urokinase-type plasminogen activ

77 II) and endothelial function (intercellular adhesion molecule-1 and vascular cell adhesion molecule-

78 oteins associated with it such as junctional adhesion molecule-1 and vascular endothelial cadherin.

79 assumed to mediate adhesion to intercellular adhesion molecule-1 for T-cell conjugation to dendritic

80 the expression of platelet endothelial cell adhesion molecule-1 in glomerular endothelial cells and

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

82 uron-specific enolase, and vascular cellular adhesion molecule-1) and 1 clinical variable (total hemo

83 adhesion molecule expression (intercellular adhesion molecule-1) and tissue infiltration of inflamma

84 MC releasate elevated ICAM-1 (intercellular adhesion molecule-1) expression on HUVEC (human umbilica

85 llular adhesion molecule-1 and vascular cell adhesion molecule-1) in 524 middle-aged women in the Nur

86 Tumour necrosis factor alpha, vascular cell adhesion molecule-1, 8-isoprostane, leptin, circulating

87 creased eosinophil adhesion to vascular cell adhesion molecule-1, caused redistribution of integrin C

88 NF-kappaB target genes VCAM-1, intercellular adhesion molecule-1, E-selectin, and tissue factor.

89 sis factor receptor-1, soluble vascular cell adhesion molecule-1, granulocyte colony-stimulating fact

90 ctive protein, fibrinogen, and intercellular adhesion molecule-1, suggested that GlycA reflects summa

91 of the proangiogenic proteins intercellular adhesion molecule-1, vascular cell adhesion protein-1, a

92 ndothelial biomarkers (soluble intercellular adhesion molecule-1: OR, 1.58; 95% CI, 1.28-1.96), white

93 ar cell adhesion molecule 1 (CADM1) and cell adhesion molecule 2 (CADM2), which encode membrane prote

94 dothelial-specific promoter of intercellular adhesion molecule 2.

95 1, and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin in macrophages

96 elial cells is mediated by the intercellular adhesion molecule-4 (ICAM-4), which appears on the RBC m

97 geting carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) for tumor delivery of 7-et

98 of claudin 1 (CLDN1), CLDN4, and junctional adhesion molecule A (JAM-A) subunits is induced at the G

99 gma1 engages glycan receptors and junctional adhesion molecule-A (JAM-A) and is thought to undergo a

100 to induce transient expression of ITGA4, an adhesion molecule actively involved in cell extravasatio

101 CD74-silenced macrophages showed that the adhesion molecules ALCAM, ICAM4, and Syndecan-2, as well

102 ely associated with activated leukocyte cell adhesion molecule (ALCAM) and C-reactive protein (CRP) (

103 Activated leukocyte cell adhesion molecule (ALCAM) is a cell adhesion molecule fo

104 Activated leukocyte cell adhesion molecule (ALCAM) is expressed on various cell t

105 Activated leukocyte cell adhesion molecule (ALCAM) mediates cell aggregation, whi

106 The dissociation rates of Cas and two other adhesion molecules, alpha-actinin and talin, were also s

107 talizumab, an antibody against the leukocyte adhesion molecule alpha4 integrin, in patients with acut

108 to the brain and spinal cord by blocking the adhesion molecule alpha4-integrin.

109 Additionally, expression of CD122 and the adhesion molecules alpha4beta7 and CD103 define distinct

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

111 CD169 is a Siglec that may function as an adhesion molecule and a facilitator of the recognition a

112 s caused by its dual functionality as a cell adhesion molecule and a signaling molecule.

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

114 ur attention on two markers, epithelial cell adhesion molecule and leucine-rich repeat-containing G p

115 ld be because of impaired expression of cell adhesion molecules and an altered cell surface glycoprot

116 protein D8 is one of three glycosaminoglycan adhesion molecules and binds to the linear polysaccharid

117 disease was driven by enhanced expression of adhesion molecules and chemokines causing the accumulati

118 hesion is mediated mainly by selectins, cell adhesion molecules and chemokines induced by pro-inflamm

119 n and IL-1 expression is the upregulation of adhesion molecules and chemokines, which leads to allogr

120 nd plays key roles in regulating NK ligands, adhesion molecules and cytokine receptors.

121 Endothelial adhesion molecules and gliosis, increased after hypoperf

122 meability, surface expression of endothelial adhesion molecules and leukocyte transmigration.

123 hanol suppressed post-ischemic expression of adhesion molecules and microglial activation.

124 lving several molecular mediators, including adhesion molecules and platelet-activating factor (PAF).

125 emia/reperfusion (I/R) injury, expression of adhesion molecules and pro- and anti-inflammatory cytoki

126 n, regulates NF-kappaB-mediated induction of adhesion molecules and proinflammatory cytokine expressi

127 TIGIT recognizes nectin and nectin-like adhesion molecules and thus plays a critical role in the

128 lung ILC2s express beta1 and beta2 integrin adhesion molecules and whether these integrins are requi

129 n with CD166/ALCAM (activated leukocyte cell adhesion molecule), and physically associates with the T

130 utations in genes encoding EpCAM, a putative adhesion molecule, and HAI-2, a cell surface protease in

131 urotransmitter receptors, cell signaling and adhesion molecules, and ciliary intraflagellar transport

132 ammatory mediator cytokines, chemokines, and adhesion molecules, and inhibition of PARP1 enzymatic ac

133 perfamily molecules such as the Aplysia cell adhesion molecule (apCAM) leads to actin filament assemb

134 Immunoglobulin superfamily adhesion molecules are among the most abundant proteins

135 g proinflammatory cytokines, chemokines, and adhesion molecules are discussed.

136 Locally, adhesion molecules are distributed at the tips of membra

137 Genes encoding cell adhesion molecules are significantly enriched in Eed(Del

138 sodium channels (VGSCs) aggregate with cell adhesion molecules at discrete subcellular locations, su

139 alpha3beta1, VE-cadherin, ICAM-2, junctional adhesion molecule-B (JAM-B), laminin, and cellular fibro

140 E-cadherin is a cell adhesion molecule best known for its function in suppres

141 ing cells, especially by overexpressing cell adhesion molecules, but also by other as yet unknown mec

142 The up-regulation of cell surface adhesion molecules by BMP9/10 in the presence of TNFalph

143 rface expression of beta1 and beta2 integrin adhesion molecules by using flow cytometry.

144 Junctional adhesion molecule C (JAM-C) is an immunoglobulin superfa

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

146 Contactin-4 (CNTN4) is a complex cell adhesion molecule (CAM) localized at neuronal membranes,

147 pends on Neuroligin 2 (NL2), a synaptic cell adhesion molecule (CAM).

148 a 24-48 hour-long response of increased cell adhesion molecules (CAM), trophic and anti-inflammatory

149 Cell adhesion molecules (CAMs) play a central role in the bar

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

151 The cadherin (cdh) superfamily of adhesion molecules carry O-linked mannose (O-Man) glycan

152 ce lacking both NF186 and the paranodal cell adhesion molecule Caspr, demonstrating that a paranodal

153 microvascular endothelial cells to stimulate adhesion molecules, CCL2, ICAM1, VCAM1 and cytokines, IL

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

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

156 49d/CD49e), chemokine receptors (CXCR4), and adhesion molecules (CD44/CD54).

157 vented the induced expression of the crystal adhesion molecules, CD44 and annexin II, in tubular epit

158 gene expression for carcinoembryonic Ag cell adhesion molecule (CEACAM) family members in the bronchi

159 the aorta in atherosclerosis is regulated by adhesion molecules, chemokines and cytokines.

160 dothelial selectin and soluble intercellular adhesion molecule concentrations decreased (P < 0.001).

161 rm of the human prion protein (PrP(c)) is an adhesion molecule constitutively expressed in the CNS.

162 Satb1 regulates expression of a homophilic adhesion molecule, Contactin 5 (Cntn5).

163 ue morphogenesis and tissue homeostasis, how adhesion molecules control cell shapes and cell patterns

164 aR-deficient mice express a reduced level of adhesion molecules, cytokines and genes associated with

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

166 Down syndrome cell adhesion molecule (Dscam) is expressed by mouse RGCs sho

167 ation marked by upregulation of cell-surface adhesion molecules E-selectin and ICAM-1.

168 RNase angiogenin, the cytokine IL18, and the adhesion molecule Embigin-and discovered that all of the

169 Epithelial cell adhesion molecule (EpCAM) is expressed at the basolatera

170 onse to contact sensitizers, epithelial cell adhesion molecule (EpCAM) on LCs promotes LC dendrite mo

171 east cancer by targeting epithelial cellular adhesion molecule (EpCAM) present on the MCF-7 cell memb

172 ated with antibodies against epithelial-cell adhesion molecule (EpCAM) via magnetic-activated cell so

173 thelial MPs, epithelial MPs (epithelial cell adhesion molecule [EpCAM](+)MPs, E-cadherin(+)MPs), plat

174 T cells are controlled by chemokines and by adhesion molecules, especially integrins, and have criti

175 red delta-protocadherins are homophilic cell adhesion molecules essential for the development of the

176 NOD-Idd22 animals expressed lower levels of adhesion molecules, even in response to inflammatory sti

177 oattractants, chemoattractant receptors, and adhesion molecules expressed by leukocytes, mucosal endo

178 This resulted in reduced pulmonary adhesion molecule expression (intercellular adhesion mol

179 Simvastatin modified surface adhesion molecule expression and activity, facilitating

180 Lower adhesion molecule expression resulted in weaker adherenc

181 ation, inflammatory cytokine, chemokine, and adhesion molecule expression, immune cell infiltration,

182 iR-100 as a potent suppressor of endothelial adhesion molecule expression, resulting in attenuated le

183 as Vegfa/VEGFR1+2 upregulation or increased adhesion molecule expression.

184 which in turn activated Rho A and the focal adhesion molecules FAK, Pyk2 and paxillin.

185 ClfB is a key adhesion molecule for the interaction of S. aureus with

186 Thus, PvGAMA may be an adhesion molecule for the invasion of Duffy-positive and

187 yte cell adhesion molecule (ALCAM) is a cell adhesion molecule found on blood-brain barrier endotheli

188 Protocadherin-10 (Pcdh10) is an adhesion molecule found to protect against tumorigenesis

189 er of carcinoembryonic antigen-like cellular adhesion molecule genes.

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

191 Adhesion molecules hold cells together but also couple c

192 Pcdh19 is known to be a homophilic cell-cell adhesion molecule, how its mutations bring about female-

193 ent adhesion of T cells to the intercellular adhesion molecule ICAM-1, with little effect on cells ex

194 ng the NFkappaB pathway and expression of EC adhesion molecules ICAM1 and VCAM1.

195 The Ig-like cell adhesion molecule (IgCAM) BT-IgSF (brain- and testis-spe

196 n as OB cadherin or CDH11) is a cell-to-cell adhesion molecule implicated in many biological function

197 Neuroligins are postsynaptic cell-adhesion molecules implicated in autism and other neurop

198 the expression of platelet endothelial cell adhesion molecule in glomerular endothelial cells and gl

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

200 iptional and immunohistological analyses for adhesion molecules in a mouse model, we identified brain

201 attenuated the expression of chemokines and adhesion molecules in endothelial cells and reduced NF-k

202 bution of specific phenotypes of T cells and adhesion molecules in exacerbated cell death in steatoti

203 rom MWCNT-exposed mice induced expression of adhesion molecules in primary murine cerebrovascular end

204 evels of ROS, proinflammatory cytokines, and adhesion molecules in SCD mice.

205 ng circulating cells to survive, upregulates adhesion molecules in target organs, recruits immune cel

206 ment, resulting from diminished induction of adhesion molecules in the graft endothelium due to incre

207 ed astrocytes, microglia, and increased cell adhesion molecules in the vasculature.

208 denovirus receptor (CAR), a single-pass cell adhesion molecule, in the adult brain.

209 irected against several region-specific cell adhesion molecules, including neurofascin, contactin and

210 F-alpha-induced expression of chemokines and adhesion molecules, including VCAM-1, IL-6, ICAM-1, E-se

211 co-expressed with ITGA3, a gene encoding the adhesion molecule integrin alpha 3.

212 In addition to interacting with each other, adhesion molecules interact with ion channels and cytoki

213 involved CD40, CD80, CD86, and intercellular adhesion molecule interactions and required production o

214 igand-1 (PSGL-1) has long been studied as an adhesion molecule involved in immune cell trafficking an

215 p of glycophosphatidylinositol-anchored cell adhesion molecules involved in the wiring of the nervous

216 ow that Cadherin-6 (Cdh6), a homophilic cell adhesion molecule, is a reliable marker of ChCs and Cdh6

217 defining molecular signature of J-RGCs, the adhesion molecule JAM-B, regulates morphogenesis, and sh

218 entially regulates intrathymic expression of adhesion molecules known to play a role in T cell progen

219 Two proteins, the neural cell adhesion molecule L1 and dipeptidyl peptidase 4, were fu

220 ly relevant to skin homeostasis: neural cell adhesion molecule L1 and dipeptidyl peptidase 4.

221 The cell adhesion molecule L1 and the extracellular matrix protei

222 ng of multiple receptors, including the cell adhesion molecule L1/NgCAM, the neurotransmitter recepto

223 hed in cell migration proteins including the adhesion molecule L1CAM.

224 ated with cell adhesion, among which L1 cell adhesion molecule (L1CAM) was significantly higher upon

225 Ps, an effect that could be modulated by the adhesion molecule laminin.

226 mined the host receptors for the multivalent adhesion molecule (MAM) from the gut commensal Escherich

227 We have previously shown that multivalent adhesion molecules (MAMs) are abundant in both pathogeni

228 tumor blood vessels, of which melanoma cell adhesion molecule (MCAM) and its extracellular matrix in

229 We further identify the melanoma cell adhesion molecule (MCAM) as a novel KDM3A target gene in

230 membrane glycoproteins, CD146/melanoma cell adhesion molecule (MCAM)/MUC18, CD31/platelet endothelia

231 Our results identify cell-adhesion molecule-mediated inhibition as a regulator of

232 g CIL requires the participation of the cell adhesion molecule N-cadherin, which starts to be express

233 d its major protein carrier, the neural cell adhesion molecule NCAM, play important roles in many ner

234 Prominent family members are the neural cell adhesion molecules NCAM and L1, which were the first to

235 rP(C) protein interactors, the neuronal cell adhesion molecule (NCAM) has been studied in vivo, but t

236 The neural cell adhesion molecule (NCAM) is the major carrier of polysia

237 is a glycan modification of the neural cell adhesion molecule (NCAM) produced by the polysialyltrans

238 gion (PBR) that are required for neural cell adhesion molecule (NCAM) recognition and subsequent poly

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

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

241 the first demonstration of a bona fide cell adhesion molecule, NECL4, regulating choline homeostasis

242 We previously showed that the cell adhesion molecule Nectin-4 is overexpressed in ovarian c

243 The synaptic adhesion molecules Neurexin and Neuroligin alter the dev

244 ipartite complexes with the presynaptic cell-adhesion molecules neurexins or 'deleted-in-colorectal-c

245 In contrast, axonal and glial nodal adhesion molecules [neurofascin-186, neuron glial-relate

246 ndent cleavage and secretion of the synaptic adhesion molecule neuroligin-3 (NLGN3), which promotes g

247 onditional deletion of the postsynaptic cell adhesion molecule neuroligin-3 in parvalbumin interneuro

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

249 e and T-cell chemoattractants, expression of adhesion molecules on the endothelial cell surface, and

250 to regulate the expression of key leukocyte adhesion molecules, on both leukocytes and endothelial c

251 h as surface antigens (e.g., epithelial cell adhesion molecule or EpCAM) or size to separate them fro

252 that molecular MRI targeting the endothelial adhesion molecule P-selectin unmasks the pathological ev

253 cy of crizanlizumab, an antibody against the adhesion molecule P-selectin, were evaluated in patients

254 ections, we investigated the function of the adhesion molecule, P-selectin glycoprotein ligand-1 (PSG

255 eceptor (pIgR) and platelet endothelial cell adhesion molecule (PECAM-1).

256 s together with those related to neural cell adhesion molecule polysialylation establish a paradigm f

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

258 tory and gut-derived factors acts as a novel adhesion molecule, present in adhesive cup structures, t

259 lled via secreted signaling factors and cell adhesion molecules provided from local niche structures.

260 Synaptic cell adhesion molecules regulate signal transduction, synapti

261 Synaptic adhesion molecules regulate synapse development and plas

262 s disease, belongs to the family of synaptic adhesion molecules (SAMs) due to its impact on synapse f

263 here a high level of the cognate ligand, the adhesion molecule SAX-7/L1, is present.

264 CP-3, and MCP-4), cell surface expression of adhesion molecules (such as VCAM-1 the ligand for VLA-4)

265 However, the interaction of Reelin with adhesion molecules, such as L1, has remained poorly expl

266 This glycoepitope is highly expressed on adhesion molecules, such as MAG, present in myelinated n

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

268 tractant protein-1, soluble endothelial cell adhesion molecule, symmetrical dimethylarginine, asymmet

269 togenetic ablation of ACs marked by the cell-adhesion molecule Teneurin-3 (Tenm3) and pharmacological

270 in determining expression of a pivotal cell adhesion molecule that may impact risks of malignant pro

271 ECL4, CADM4) is a Schwann cell-specific cell adhesion molecule that promotes axo-glial interactions.

272 These include VE-cadherin, a homotypic adhesion molecule that regulates endothelial barrier fun

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

274 Neuroligins are postsynaptic cell-adhesion molecules that bind to presynaptic neurexins.

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

276 e evolutionarily conserved postsynaptic cell adhesion molecules that interact with presynaptic neurex

277 ring is thought to depend on two axonal cell adhesion molecules that mediate interactions between the

278 exploitable therapeutic target; however, the adhesion molecules that specifically regulate the step o

279 rtebrate Dscams (DSCAM and DSCAML1) are cell adhesion molecules that support the development of this

280 e present study investigated the role of the adhesion molecules, their porcine ligands, and the chemo

281 Egfl7 regulates the expression of these adhesion molecules through the NF-kappaB and MEK/Erk pat

282 hich the folate receptor interacts with cell adhesion molecules, thus regulating the apical cell memb

283 proximately 40 gene families, including cell-adhesion molecules, transmitter-modulator receptors, ion

284 e up-regulation of endothelial selectins and adhesion molecules, ultimately resulting in increased mo

285 erferon (IFN-alpha), key cytokines, and cell adhesion molecules (vascular cell adhesion molecule 1 [V

286 d by the reduced expression of vascular cell adhesion molecule (VCAM)-1 in human cultured endothelial

287 pression levels of E-selectin, vascular cell adhesion molecule (VCAM-1), and intercellular adhesion m

288 cluding soluble plasma vascular and cellular adhesion molecules (VCAM-1 and ICAM-1, respectively), ma

289 eins (fibrinogen, haptoglobin and CRP), cell adhesion molecules (VCAM-1), endothelial growth factors

290 te adhesion to ECs by reducing expression of adhesion molecule VCAM1.

291 senescence, expression of chemokines and the adhesion molecule VCAM1.

292 troscopy and modeling have revealed that the adhesion molecule vinculin and F-actin form a catch bond

293 anistically, the tension sensing cell-matrix adhesion molecule, vinculin, and the Rho/ROCK pathway, w

294 D122(-)PD1(+)CD44(+)CD62L(-)) and expressing adhesion molecules (VLA-4(+)LFA-1(+)) complementary to a

295 pression of Toll-like receptors and cellular adhesion molecules were evaluated by fluorometric enzyme

296 uited to the wounded amnion where macrophage adhesion molecules were highly expressed.

297 ic inflammatory markers and soluble vascular adhesion molecules were measured in plasma samples of da

298 lood neutrophil apoptosis, phagocytosis, and adhesion molecules were quantified by flow cytometry, an

299 target genes encode diverse epithelial cell adhesion molecules, while mesenchymal genes involved in

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