ライフサイエンスコーパス: cell adhesion

1 involved in their reorganization to sites of cell adhesion.

2 n structure, stability, and activity such as cell adhesion.

3 ial monolayer wound repair and reduce immune cell adhesion.

4 or which it is specific, as well as APC-to-T-cell adhesion.

5 the functions of specific talin isoforms in cell adhesion.

6 roteins, Wnt/PCP signaling pathway, and cell-cell adhesion.

7 n CEACAM5, a tumor marker and facilitator of cell adhesion.

8 atenin isoform 1A phenotype and reduced cell-cell adhesion.

9 in SPRY motifs that are not involved in cell-cell adhesion.

10 ction in both actin filament disassembly and cell adhesion.

11 ulated integrin recycling, thereby promoting cell adhesion.

12 g, increased integrin activity, and enhanced cell adhesion.

13 reases membrane E-cadherin and restores cell-cell adhesion.

14 sin cytoskeleton and cell expansion via cell-cell adhesion.

15 of three-dimensional models in studying cell-cell adhesion.

16 e adhesion dominate over those favoring cell-cell adhesion.

17 ar component organization, cell motility and cell adhesion.

18 rate-based motility be coordinated with cell-cell adhesion.

19 OBO2 in cultured mouse podocytes compromises cell adhesion.

20 estor when an ancestral gene is co-opted for cell adhesion.

21 activity and regulation, apoptosis and cell-cell adhesion.

22 containing two tandem PDZ domains mediating cell adhesion.

23 chanistic insights into how DECMA-1 disrupts cell adhesion.

24 s and the increased Ca(2+)-cross linked cell-cell adhesion.

25 ng with cell-spreading assays to investigate cell adhesion.

26 elling and intracellular pathways related to cell adhesion.

27 orm switching and associated changes in cell-cell adhesion.

28 lays a fundamental role in integrin-mediated cell adhesion.

29 n they die, but some toxic compounds promote cell adhesion.

30 munostained samples colocalized with FliI at cell adhesions.

31 tered by modulating the cell-matrix and cell-cell adhesions.

32 th the inherent benefit of resisting protein/cell adhesions.

33 l killing (24% vs 50%), increased epithelial cell adhesion (31.6% vs 17.8%) and upregulation of adhes

34 transcriptional pathway triggered by loss of cell adhesion activates lysosomes in C. elegans epidermi

35 n of alginate and puramatrix, which promoted cell adhesion and aggregation.

36 o major hallmarks of cancer, loss of cell-to-cell adhesion and anchorage-independent growth, are both

37 is induction is necessary for vIL-6-mediated cell adhesion and angiogenesis, suggesting a potential r

38 h cells lose epithelial traits, such as cell-cell adhesion and apico-basal polarity, and acquire migr

39 y and repair due to environmental stress and cell adhesion and barrier integrity.

40 hysiological regulation of keratinocyte cell-cell adhesion and blister development.

41 There is growing evidence that both cell adhesion and cell detachment can modulate autophagy

42 that this pool of ceramide acutely regulates cell adhesion and cell migration pathways with weak conn

43 r necessary and sufficient for regulation of cell adhesion and cell migration under chemotherapeutica

44 regulatory role for PI4KIIIbeta and PI4P in cell adhesion and cell shape maintenance.

45 n healthy tissues strongly relies on cell-to-cell adhesion and cell-to-extracellular matrix interacti

46 1), a membrane protein that mediates cell-to-cell adhesion and communication, as a mechanism through

47 Cell shape is regulated by cell adhesion and cytoskeletal and membrane dynamics.

48 espread down-regulation of genes involved in cell adhesion and cytoskeleton organization, resulting i

49 ification, suggesting that defective cell-to-cell adhesion and dysfunction of the movement of solutes

50 ase in MPC genes associated with pathways of cell adhesion and ECM-receptor interactions, and MPC tra

51 (AJs) is essential for the formation of cell-cell adhesion and epithelium integrity; however, studyin

52 inergic activity, which inhibits BM vascular cell adhesion and homing.

53 n by Dkk1 concomitantly drives repression of cell adhesion and inhibits beta-catenin-dependent transc

54 cells in vivo, including loss of epithelial cell adhesion and junction genes.

55 local topographic interactions to strengthen cell adhesion and large surface areas for grafting captu

56 wn-regulated expression of genes involved in cell adhesion and markers of decidualisation.

57 and-binding domains in adhesins that support cell adhesion and migration in many eukaryotic phyla.

58 on of collagen fibrils is known to impact on cell adhesion and migration in the context of cancer and

59 Both effects are highly relevant for cell adhesion and migration within the tumour microenvir

60 and localized process that can contribute to cell adhesion and migration.

61 SK3B and L1CAM that are involved in neuronal cell adhesion and migration.

62 iate these "side" effects of chemotherapy on cell adhesion and migration.

63 isrupting long neural genes involved in cell-cell adhesion and migration.

64 llular processes including the regulation of cell adhesion and migration.

65 3 cells enriched in proteins associated with cell adhesion and migration.

66 can play a role in other processes, such as cell adhesion and motility.

67 These activating mAbs increase cell adhesion and reduce cell invasion and migration in

68 ein involved in protein ectodomain shedding, cell adhesion and signalling.

69 n of PTRF led to MAPKi resistance, increased cell adhesion and sphere formation.

70 CDH6 protein is implicated in cell adhesion and synaptogenesis while HAGH protein is r

71 Taking advantage of the strong homologous cell adhesion and uptake, l-G@SeNPs have been shown here

72 , collectively migrating cells maintain cell-cell adhesions and coordinate direction-sensing as they

73 ncluding ESCRT-mediated membrane remodeling, cell adhesion, and apoptosis.

74 nd presentation, methyltransferase activity, cell adhesion, and cell junctions.

75 terms that are related to the cytoskeleton, cell adhesion, and cell migration.

76 nscriptomic changes affecting cell motility, cell adhesion, and cytoskeleton organization.

77 terial activity, type-1 fimbriae expression, cell adhesion, and invasion and intestinal colonization

78 resulting in defective integrin activation, cell adhesion, and migration.

79 mportant role in many cell functions such as cell adhesion, and migration.

80 is involved in local cell alignment and cell-cell adhesion, and that reduction of HyFatl leads to def

81 ant for the determination of cell phenotype, cell adhesion, and tissue regulation and signaling.

82 er categories such as "cell proliferation," "cell adhesion," and "apoptosis." Cell-type-association a

83 pp5a- and Rab11a-mediated resolution of cell-cell adhesions are both necessary for midline lumen open

84 genes involved in migration, chemotaxis, and cell adhesion as well as induction of a proinflammatory

85 The latter may be due to altered cell adhesion, as loss of Pxt or Fascin, or coreduction

86 ests a wider prevalence of heterophilic cell-cell adhesion-based ECD regulation during animal morphog

87 Cell-cell adhesion-based ECD, however, has not yet been clear

88 this mechanism of dynamic heterophilic cell-cell adhesion-based regulation of ECD.

89 r network that yields qualitative degrees of cell adhesions by adherens junctions and focal adhesions

90 catenin, a component of the cadherin-catenin cell adhesion complex, promotes coordination of growth a

91 xtracellular matrix (ECM), cell-ECM and cell-cell adhesion complexes influence metabolic pathways.

92 k components of the Wnt/PCP pathway and cell-cell adhesion complexes raising the question if ctenopho

93 alpha-Catenin links cell-cell adhesion complexes to the actin cytoskeleton, and m

94 independent role for MASTL as a regulator of cell adhesion, contractility, and MRTF-A/SRF activity.

95 10%), showing enrichment in cell migration, cell adhesion, developmental process, synapse assembly,

96 e during cell separation and augmenting cell-cell adhesion does not impede detachment.

97 lity by simple optical imaging using "single cell adhesion dot arrays" (SCADA), fibronectin (FN) dot

98 he central role of forces in regulating cell-cell adhesions during collective motility.

99 n shown to influence hormone signaling, cell-cell adhesion, epithelial-to-mesenchymal transition, tra

100 The FMCR assay allowed us to analyze the cell-adhesion events from these different treatment cond

101 factors; transcriptional regulators; cell-to-cell adhesion; extracellular matrix), suggesting that th

102 asuring, in parallel, hundreds of individual cells' adhesion forces with a resolution at the pN level

103 that re-expression of APC restores the cell-cell adhesion gene and posttranscriptional regulatory pr

104 ternatively spliced ZMAT3 target was CD44, a cell adhesion gene and stem cell marker that controls tu

105 full-length, wild-type APC (fl-APC) on cell-cell adhesion genes and p120-catenin isoform switching i

106 Disrupting various cell adhesion genes markedly reduces cluster formation a

107 ated expression of gene sets such as ECM and cell adhesion genes occurs in C9 and sporadic ALS but no

108 h HSPCs showed significant downregulation of cell adhesion genes, consistent with enhanced egress of

109 thin a cell aggregate, and differential cell-cell adhesion has been proposed to explain this behavior

110 ma membrane, and inhibited integrin-mediated cell adhesion in a Tyr45-dependent fashion.

111 that regulate planar cell polarity (PCP) and cell adhesion in bilaterians.

112 animals [8-11]; however, whether it mediates cell adhesion in non-metazoan taxa remains unknown.

113 positioning, extracellular matrix, and cell-cell adhesion in shaping Drosophila wing imaginal discs.

114 CAV1 protein abundance, or integrin-mediated cell adhesion in strumpellin-deficient cells.

115 ell identity and patterning mediated through cell adhesion in the developing cochlea.

116 ate chromatin structure, RNA metabolism, and cell adhesion, including a focal adhesion kinase (FAK)-r

117 sses cell polarization and integrity of cell-cell adhesion, independently of its impact on beta-caten

118 g levels of homophilic E-cadherin-based cell-cell adhesion induce cell sorting, but not ECD.

119 ctional analysis were mainly associated with cell adhesion, inflammatory response, and extracellular

120 xyacetophenone (4-HAP) inhibits colon cancer cell adhesion, invasion, and migration in vitro and redu

121 undles in the actin cortex are important for cell adhesion, invasion, and migration.

122 Cell-cell adhesion is a key mechanism to control tissue integ

123 cating that in social yeasts Flo11A-mediated cell adhesion is a major mechanism for kin discriminatio

124 Cadherin-mediated cell-cell adhesion is actin-dependent, but the precise role o

125 Here we show that loss of cell-cell adhesion is correlated with inactivation of RAP1 co

126 he precise role of actin in maintaining cell-cell adhesion is not fully understood.

127 As a consequence, cell adhesion is strengthened, limiting the migration of

128 in Myospheroid, which is necessary for basal cell adhesion, is mislocalized in Sac1(ts) retinas.

129 In the absence of E-cadherin-mediated cell adhesion, LC numbers remained stable and similar as

130 as type I and II interferon signaling, cell-cell adhesion, leukocyte chemotaxis, and angiogenesis.

131 Cell adhesion mediated by selectins (expressed by activa

132 to a significant decrease in colon carcinoma cell adhesion, migration and metastasis.

133 pulation and established epicardial roles in cell adhesion, migration, and chemotaxis as a mechanism

134 These processes are essential for cell adhesion, migration, and organ development.

135 h cell-surface integrin receptors to promote cell adhesion, migration, and proliferation.

136 ade, specifically within tumor angiogenesis, cell adhesion, migration, epithelial-to-mesenchymal tran

137 pede integrin-associated functions including cell adhesion, migration, or contraction.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 (2019) identify the cell adhesion molecule L1CAM as integral to the mechanis

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

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

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

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

181 This study demonstrates that cell adhesion molecule transmembrane and immunoglobulin

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

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

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

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

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

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

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

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

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

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

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

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

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

195 : 1.30 mmol/L; P = 0.021), and intercellular cell adhesion molecule-1 (WA: 153.9 ng/mL; CB: 159.4 ng/

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

217 Differences in cell adhesion molecules and leukocyte adhesion were abla

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

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

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

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

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

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

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

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

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

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

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

229 the tripeptide arginyl-glycyl-aspartic acid cell adhesion motif RGD, which can be used as coating, b

230 teins, associated with protein folding, cell-cell adhesion, NADH dehydrogenase activity, ATP-binding,

231 Desmosomes are cell-cell adhesions necessary for the maintenance of tissue i

232 of talin1, a key regulator of integrins and cell adhesions, negatively correlated with the survival

233 e, telomere maintenance, signaling, and cell-cell adhesion.Objectives: To improve our understanding o

234 nockout eliminated the stimulatory effect of cell adhesion on Oxo-M-stimulated glucose-stimulated ins

235 We show that cell adhesion on three-dimensional curvatures induces a

236 Rap-1 mediates cell adhesion, polarization, and directional motility, a

237 y through the regulation of phrenic-specific cell adhesion programs.

238 ent and uncouple novel FGFR kinase-dependent cell adhesion properties from canonical intracellular si

239 By analysing cell adhesion properties, we demonstrate that Elkin1 del

240 he integrity of the EVL, likely by mediating cell adhesion properties.

241 g by the human version of the essential cell-cell adhesion protein alphaE-catenin but not its homolog

242 stically ascribed to increased levels of the cell adhesion protein E-CADHERIN, which lead to prematur

243 k of ILCs is the functional loss of the cell-cell adhesion protein E-cadherin.

244 ich the cytosolic C terminus of the synaptic cell adhesion protein Neuroligin-2 alters the conformati

245 ular region of E-cadherin, an essential cell-cell adhesion protein.

246 neurexin-1alpha (Nrxn1alpha), a presynaptic cell-adhesion protein implicated in ASDs.

247 ry vascular cell adhesion molecule 1 (VCAM1) cell-adhesion protein.

248 pses requires the intimate interplay between cell adhesion proteins, scaffold and adaptor proteins, a

249 the cadherin family of Ca(2+)-dependent cell-cell adhesion proteins, which play essential roles in an

250 s the coordinated action of Vangl2, Ezrb and cell-adhesion proteins to inhibit blebs and promote pola

251 nd impairment of CAV1- and integrin-mediated cell adhesion, providing insights into the cellular path

252 s a subunit member of the integrin family of cell adhesion receptors and was found to activate comple

253 Teneurins are ancient metazoan cell adhesion receptors that control brain development a

254 t cell-expansive forces of heterophilic cell-cell adhesion regulate ECD: higher cell-cell adhesion re

255 l formalism of the molecular clutch model of cell adhesion, regulated by local mechanical forces, I s

256 family members, which are all important cell-cell adhesion regulators.

257 Analysis of cell-cell adhesion-related proteins in SW480+APC cells reveal

258 t FGF functions such as cell-matrix and cell-cell adhesion remained unaffected, though these activiti

259 and vasoconstriction, but its involvement in cell-adhesion remains largely unknown.

260 cell-cell adhesion regulate ECD: higher cell-cell adhesion results in cell size enlargement.

261 Functional studies included endothelial cell adhesion, shear stress-induced cell alignment, bloo

262 y of which play critical roles in apoptosis, cell adhesion, signal transduction, or metabolite homeos

263 and that neurolign-1-mediated trans-synaptic cell adhesion signaling critically regulates LTP.

264 Molecular mechanisms related to cell adhesion signaling have been extensively studied, e

265 well-characterized regulator of mesenchymal cell adhesion signaling, F-actin cytoskeleton remodeling

266 e expected to impact on the accessibility of cell adhesion sites and altered fibril surface charge on

267 icrotubule (MT)-based cytoskeletons at these cell adhesion sites.

268 and Fat-like cadherins have ancient roles in cell adhesion, spindle orientation, and tissue organizat

269 Real-time measurement of cell adhesion, stiffness, and imaging were performed usi

270 in mechanistically how gut microbes regulate cell adhesion strength at high shear stress through intr

271 strate adhesion and decreased homotypic cell-cell adhesion strength.

272 but not N-cadherin-dependent homophilic cell-cell adhesion, suggesting that other N-cadherin-binding

273 Osteocyte cell adhesion supports FAK tyrosine phosphorylation, and

274 processes while transcripts associated with cell adhesion, synaptic vesicle transport, regulation of

275 eometries that generated local nodes of high cell-adhesion tension directed the spatial patterning of

276 rins in regulating cytoskeletal dynamics and cell adhesion that predates their role as axon guidance

277 molecules, as well as proteins involved with cell adhesion, the cytoskeleton, and apoptosis, were inc

278 nding protein-like (TB) domains and mediates cell adhesion through integrin binding to the RGD motif

279 at depletion of either Scrib or Lgl1 affects cell adhesion through the inhibition of focal adhesion d

280 ic antibody for integrin beta2, we inhibited cell adhesion to a fibronectin-coated surface.

281 in response regulates autophagy, connecting cell adhesion to autophagy.

282 tribution of peripheral T cells, including T-cell adhesion to blood vessel endothelium, endothelial a

283 s, we demonstrate that ITGA2 triggers cancer cell adhesion to collagen, promotes cell migration, anoi

284 anobodies that mediate antigen-specific cell-cell adhesion to effectively overcome the barrier to T6S

285 This study proposes T-cell adhesion to endothelial cells as a necessary but in

286 lity of each RGD-binding integrin to mediate cell adhesion to fibrillin-1 or a disease-causing varian

287 ICAM1 antibody significantly inhibited tumor cell adhesion to HEC in wild-type mice confirming that N

288 Wnt5a promoted ovarian tumor cell adhesion to peritoneal mesothelial cells as well as

289 n tumor cells, endothelial activation, tumor cell adhesion to the endothelium, and recruitment of met

290 Results show that OvCa cell adhesion to the peritoneum was increased under comp

291 diated drug resistance, which depends on ALL cell adhesion to the stroma through adhesion molecules,

292 adherens junctions in order to maintain cell-cell adhesion under contraction.

293 sine kinase and Canoe/Afadin that stabilizes cell adhesion under tension at tricellular junctions in

294 Arterial myeloid cell adhesion was quantified by intravital microscopy.

295 infection was associated with enrichment in cell adhesion, whereas parasite removal was associated w

296 d the expression of genes implicated in cell-cell adhesion, whereas the expression of negative regula

297 PDMS nanobrush can either promote or inhibit cell adhesion, which is required for various biomedical

298 tumor invasion through an influence on cell-cell adhesion within the tumor and highlight the importa

299 n of toxic effects of compounds that promote cell adhesion would constitute a step forward toward hig

300 linked to mutations in genes regulating cell-cell adhesion, yet mouse models have largely failed to r