ライフサイエンスコーパス: cell adhesion

1 levels of cortical F-actin and enhanced cell-cell adhesion.

2 ajor players in YAP1 regulation triggered by cell adhesion.

3 understanding of the molecular mechanisms of cell adhesion.

4 the canonical Wnt pathway and is critical in cell adhesion.

5 , the maintenance of beta-cell identity, and cell adhesion.

6 eased cytoskeletal tension and impaired cell-cell adhesion.

7 ganization and membrane dynamics during cell-cell adhesion.

8 esenchymal phenotype and an increase in cell-cell adhesion.

9 d entail the loss of epithelial polarity and cell adhesion.

10 e cytoskeleton, intercellular junctions, and cell adhesion.

11 lamellipodial protrusion, phagocytosis, and cell adhesion.

12 tion of WNT/beta-catenin pathway and loss of cell adhesion.

13 ins of CDH23 and is predicted to impair cell-cell adhesion.

14 n in LV12 cells attenuated liver endothelial cell adhesion.

15 -affinity homophilic bonds that promote cell-cell adhesion.

16 to control CdGAP residence at sites of cell-cell adhesion.

17 Instead, it regulates cell migration and cell adhesion.

18 bimolecular interactions that maintain cell-cell adhesion.

19 its partner protein TraB to function in cell-cell adhesion.

20 TSN1 that bind GPR124 blocked GPR124-induced cell adhesion.

21 aptor molecule (RIAM)-dependent increases in cell adhesion.

22 usion protein containing E2 domain inhibited cell adhesion.

23 ncodes a cell wall protein that imparts cell-cell adhesion.

24 protein-carbohydrate interactions, and cell-cell adhesion.

25 the desmosome and known for its role in cell-cell adhesion.

26 integrin by talin is essential for inducing cell adhesion.

27 tion of actin cytoskeleton dynamics and cell-cell adhesion.

28 th cadherins can interact with each other in cell adhesion.

29 ure of compact tissues held together by cell-cell adhesion.

30 cytosolic tail and thereby localizes at cell-cell adhesions.

31 nd a reduction in alpha/beta-catenin at cell-cell adhesions.

32 but not the maintenance of established cell-cell adhesions.

33 Here, we focus on epithelial cell-cell adhesion, a critical but understudied process in se

34 w that ectopic expression of GPR124 promotes cell adhesion, additive to extracellular matrix-dependen

35 expression of multiple genes associated with cell adhesion, among which L1 cell adhesion molecule (L1

36 In addition, it regulates cell-to-cell adhesion, AMPK signaling, autophagy and apoptosis i

37 During cell adhesion, an active multistage process naturally le

38 to the tight junction (TJ), the apical cell-cell adhesion and a key regulator of the epithelial barr

39 bility and biological-recognition motifs for cell adhesion and angiogenesis.

40 pical junctional complex genes that regulate cell adhesion and apical constriction.

41 poorly understood changes in epithelial cell-cell adhesion and cell motility.

42 dy upends the clear distinction between cell-cell adhesion and cell-matrix adhesion by showing that t

43 differentially methylated genes function in cell adhesion and communication pathways.

44 tive contributions of osmotic pressure, cell-cell adhesion and cortical stiffness to mitotic rounding

45 y terms related to the extracellular matrix, cell adhesion and cytoskeleton.

46 single-organism process, catalytic activity, cell adhesion and enriched in ECM-receptor interaction,

47 ed with S-GlcNAc are mainly involved in cell-cell adhesion and gene expression.

48 iding a more beneficial microenvironment for cell adhesion and growth.

49 biofilm formation with augmented epithelial cell adhesion and higher levels of bacterial colonizatio

50 In turn, cell adhesion and invasion abilities were significantly

51 C1QBP may regulate RCC cell adhesion and invasion through influencing the p-GSK

52 ag2, which controls integrin endocytosis and cell adhesion and is impaired in cancer and developmenta

53 -catenin signaling pathway, its role in cell-cell adhesion and liver function, and the cell type-spec

54 in QRsP-11 cells increased liver endothelial cell adhesion and liver metastasis.

55 ene-expression program related to signaling, cell adhesion and locomotion; it achieved this in part b

56 r protein kindlin-2 plays a central role for cell adhesion and membrane protrusion by directly bindin

57 membrane trafficking, resulting in impaired cell adhesion and migration in vitro.

58 ests that NUAK1 is an important regulator of cell adhesion and migration, cellular and organismal met

59 f GBPs, is also engaged in the regulation of cell adhesion and migration.

60 a novel role of Galphai-GTP in regulation of cell adhesion and migration.

61 les such as mediating cellular receptors and cell adhesion and migration.

62 l function for this kinase as a modulator of cell adhesion and migration.

63 differentiation, including genes involved in cell adhesion and migration.

64 reby regulating cellular processes including cell adhesion and migration.

65 of developing organs to regulate dynamics of cell adhesion and motility during epithelial branching m

66 ds have been associated with regulating cell-cell adhesion and motility, and thus have a critical rol

67 ard in dental materials, do not support stem cell adhesion and negatively impact matrix and signaling

68 Both cell-cell adhesion and oriented cell division play prominent

69 gative regulator of beta2 integrin-dependent cell adhesion and reactive oxygen species production but

70 As polySia modulates cell adhesion and signaling, immune cell function, and t

71 Sertoli cells so that they failed to support cell adhesion and transport of germ cells and organelles

72 in products that regulate immune function or cell adhesion and tumor cell metastasis.

73 /Rac1 GTPase and protein kinase A targets at cell adhesions and cytoskeleton: VE-cadherin, p120-caten

74 in innate and adaptive immunity, chemotaxis, cell-adhesion and transcription regulation, which are bi

75 inding strongly impairs integrin activation, cell adhesion, and cell spreading.

76 ed in loss of cortical F-actin, reduced cell-cell adhesion, and disrupted localization of adhesion-as

77 s related to increased extracellular matrix, cell adhesion, and epithelial-to-mesenchymal transition.

78 tern, reduced proliferation, normalized cell-cell adhesion, and formation of crypts in tissue culture

79 ue to cell elastic distortion, offset by tip-cell adhesion, and indeed such a model fits the bare-tip

80 ls, promoting neutrophil infiltration, tumor cell adhesion, and metastasis.

81 in PDA pathways, including axon guidance and cell adhesion, and newly identified processes, including

82 aling pathways that regulate cell migration, cell adhesion, and proliferation.

83 does not depend on the absolute strength of cell adhesion, and similar gaps are predicted to occur i

84 ription factor activity, protein metabolism, cell adhesion, and vascular development, among others.

85 e coordinated action of actin networks, cell-cell adhesions, and cell-extracellular matrix (ECM) adhe

86 143 and miR-145 target genes associated with cell adhesion, apoptosis and proliferation were measured

87 A quantitative 3D cell-cell adhesion assay and live cell imaging of cell-cell c

88 ingly, the expression of Cx50 alone promoted cell adhesion at a comparable level to AQP0; however, th

89 hese cytoskeletal networks failed to support cell adhesion at the BTB.

90 nstead, a combination of local prevention of cell adhesion at three-cell junctions by fluidlike extra

91 ERbeta-regulated factors are involved in cell adhesion, axon guidance, and signaling of Notch and

92 icroglia were enriched for genes involved in cell adhesion, axonal guidance, cell surface receptor ex

93 blies at the cell surface and programed cell-cell adhesion between homotypic and heterotypic cells vi

94 dependent regulation of DE-Cadherin-mediated cell adhesion between NBs and neighboring cortex glia, a

95 rge number of surface receptors that mediate cell adhesion between RBCs, and between RBCs and white b

96 in vitro gastrointestinal resistance, Caco-2 cell adhesion), bioactivity and microstructure were anal

97 Thus, sorting is sensitive to cell adhesion but not to stiffness or cell size.

98 tify kindlin-2 as a key protein that couples cell adhesion by activating integrins and the induction

99 ional target of Hh signaling to control cell-cell adhesion by negative regulation of E-cadherin expre

100 Furthermore, disruption of cell adhesion by the E2 domains impaired primary lens ce

101 Reduction of cell adhesion by the knockdown of C-cadherin increased g

102 Here we tested the modulation of cell-cell-adhesion by extracellular pH and NHE1.

103 Moreover, loss of cell-cell adhesion caused up-regulation of cell-ECM adhesion,

104 te transendothelial migration, angiogenesis, cell adhesion, cell polarity, spermatogenesis, and metas

105 s patients, related to epigenetic control of cell adhesion, chemotaxis, cytoskeletal reorganisations,

106 ng and induction of the alpha4beta1 integrin cell adhesion complex in hematopoietic stem and progenit

107 Mechanical cues are sensed and transduced by cell adhesion complexes to regulate diverse cell behavio

108 ing forces transmitted via integrin-mediated cell adhesion, consistent with the need for larger inter

109 a reduction in inhibitors, and the improved cell adhesion could be attributed to preservation of rel

110 n modes can interconvert based on changes in cell adhesion, cytoskeletal mechanotransduction [5], and

111 These encompass proteins involved in cell adhesion, cytoskeleton regulation and vesicle-media

112 transmembrane protein with critical roles in cell adhesion, cytoskeleton remodeling and nuclear archi

113 This approach improves the efficiency of cell adhesion due to force attachment.

114 ds, where it enhances cell motility and cell-cell adhesion dynamics.

115 s related to extracellular matrix, immunity, cell adhesion, epigenetic regulation, and airflow obstru

116 ified a new role for Cx50 that mediates cell-cell adhesion function.

117 in this study that latrophilin-2 (Lphn2), a cell-adhesion G protein-coupled receptor and presumptive

118 ity in C. elegans, we identified and studied cell adhesion genes expressed in three interacting neuro

119 umors revealed that extracellular matrix and cell adhesion genes, including collagen II (Col2a1), wer

120 Cell adhesion genes, JAM-A and FSCN1, were downregulated

121 anization, small molecule metabolic process, cell adhesion (GO IDs: 0030198, 0044281, 0007155) and pa

122 x glycosaminoglycans have important roles in cell adhesion, growth, proliferation and repair, and the

123 a the IQGAP1-Rac1 pathway to strengthen cell-cell adhesion in normal adult crypt stem cells and colon

124 hannels regulate beta1-integrin function and cell adhesion in rheumatoid arthritis fibroblast-like sy

125 pact on the actin cytoskeletal structure and cell adhesion in the absence of RSPO stimulation, but th

126 th ICAM-1 to mediate cancer cell-endothelial cell adhesion in the case of the more invasive BCs.

127 ays are reviewed at the level of (1) clastic cell adhesion in the external apical root resorption pro

128 n with CD6 and weaker homophilic CD166-CD166 cell adhesion interaction.

129 3D cell-based simulation with realistic cell-cell adhesion, interaction forces, and chemotaxis.

130 e (Ccl2, Ccl7, Cxcl1, Cxcl2, and Cxcl10) and cell-adhesion (intracellular adhesion molecule 1 and vas

131 hin a small energetic range, suggesting that cell adhesion is an elaborately designed process in whic

132 We found that beta1 integrin-dependent cell adhesion is critical for supporting cell proliferat

133 ed, but rigidity sensing by cadherins during cell adhesion is largely unexplored.

134 trix fluid at three-cell junctions such that cell adhesion is locally disrupted and a tension differe

135 As no cell-adhesion ligands are presented by the hydrogels, th

136 t cells have stronger FAK phosphorylation in cell adhesions, long-lasting trailing ends and slower tu

137 al connection between cell polarity and cell-cell adhesion machineries in mammalian cells.

138 herin), a protein that plays a vital role in cell adhesion, making it a biologically plausible candid

139 Cell adhesion markers were assessed.

140 igration and stromal interactions and revert cell adhesion-mediated drug resistance (CAM-DR) to the s

141 k between intracellular annexin A2 and tumor cell adhesion, migration and in vivo grafting.

142 otein that promotes tissue remodeling, tumor cell adhesion, migration and invasion.

143 ix through protease recruitment and enhances cell adhesion, migration and signaling through vitronect

144 henotype, which, in turn, facilitates cancer cell adhesion, migration, and invasion.

145 We show that KLF4 promotes cell adhesion, migration, and morphological changes, all

146 rtain RGD-binding integrins are required for cell adhesion, migration, and proliferation and are over

147 cell surface, and plays an important role in cell adhesion, migration, and proliferation.

148 al activation of integrin and, consequently, cell adhesion, migration, in vitro endothelial tube form

149 this mutation had moderate abnormalities in cell adhesion, migration, proliferation and growth facto

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

198 The cell adhesion molecule L1 and the extracellular matrix p

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

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

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

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

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

204 -519d in determining expression of a pivotal cell adhesion molecule that may impact risks of malignan

205 4 (NECL4, CADM4) is a Schwann cell-specific cell adhesion molecule that promotes axo-glial interacti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

249 The following are considered: cell adhesion motifs, structural peptides, cell-penetrat

250 Fundamental processes in cell adhesion, motility, and rigidity adaptation are reg

251 lular mechanisms leading to the loss of cell-cell adhesion, new ideas were shared in the field of sig

252 We show a clear dependence of melanoma cell-cell adhesion on pHe and NHE1 as a modulator.

253 der flow: PD1n-3 DPA and RvD5n-3 DPA reduced cell adhesion onto TNF-alpha-activated human endothelial

254 t induction of pattern recognition receptor, cell adhesion, or chemotaxis genes in macrophages.

255 gy studies have shown that cell-ECM and cell-cell adhesions participate in mechanosensing to transduc

256 demonstrate that in addition to its role in cell adhesion, PKP2 is necessary to maintain transcripti

257 Periostin and vascular cell adhesion protein 1 (VCAM-1), molecules that mediate

258 Here, we demonstrate that the cell-cell adhesion protein E-cadherin functions as an instruc

259 intercellular adhesion molecule-1, vascular cell adhesion protein-1, and VEGF.

260 A number of widely-conserved cell adhesion proteins are implicated in cell recognitio

261 The neuroligin family cell adhesion proteins NL1, NL2, and NL3, which are expr

262 o and lung metastatic capability in vivo The cell adhesion receptor EphA4 was determined to be a dire

263 ents to our knowledge the first example of a cell adhesion receptor exhibiting retrograde nuclear tra

264 This dual role for a cell adhesion receptor permits the cell to functionally

265 dinated cytoskeletal dynamics contributes to cell adhesion regulation during intestinal wound repair

266 ters of T, NANOS3, and SOX17) and the RREB-1 cell adhesion regulator.

267 n vivo and in vitro beta1 integrin-dependent cell adhesion relied on the relocation of YAP1 to the nu

268 But most effective cell adhesion separation technologies use labels or long

269 Cell adhesion status was also affected by changes in mit

270 ion and NHE1 overexpression both reduce cell-cell adhesion strength, indicated by reduced maximum pul

271 in plays a critical role in endothelial cell-cell adhesion, thereby controlling endothelial permeabil

272 signaling pathway where SDF-1alpha induces T-cell adhesion through activation of PLCepsilon1, suggest

273 ar to be the key specializations that enable cell adhesion through integrins to be coordinated with c

274 Cell adhesion to a 30-kPa Ecad-Fc PA gel required Cdc42-

275 26 and miR-126* enhanced firm monocyte and T cell adhesion to hCMEC/D3 cells, whereas their increased

276 diated rolling facilitates pancreatic cancer cell adhesion to hyaluronic acid.

277 Thus, Amigo2 regulated tumour cell adhesion to liver endothelial cells and formation o

278 Talin1 depletion impaired cancer cell adhesion to the endothelium and transendothelial mi

279 onocyte MMP secretion in pulmonary TB during cell adhesion to the extracellular matrix (ECM).

280 Mammalian cell adhesion to the extracellular matrix influences num

281 Cell adhesion to the extracellular matrix or to surround

282 associations of astral microtubules at cell-cell adhesions to orient the mitotic spindle.

283 igration, transmigration through endothelial cells, adhesion to stromal cells, and cell proliferation

284 this process by coupling cadherin-based cell-cell adhesion together with actomyosin contractility.

285 A better understanding of tumor cell adhesion under physiologic shear would lead to the

286 barrier formation, cytoskeletal tension, and cell adhesion, underscoring the complexity of signaling

287 matrix component, enables integrin-mediated cell adhesion via binding of alpha5beta1, alphaIIbbeta3

288 y, our results indicate that GPR124 promotes cell adhesion via Elmo-Dock and ITSN.

289 ct of IFNgamma on HSCs, which indicates that cell adhesion via integrin alphavbeta3 within the BM nic

290 the upstream regulation of integrin-mediated cell adhesion via the control of focal adhesion remodeli

291 This effect on cell adhesion was molecularly supported by the regulatio

292 showed that E-cadherin-dependent epithelial cell adhesion was sensitive to changes in PA gel elastic

293 glycosylation is an important determinant of cell adhesion, we hypothesized that radiation could alte

294 some genes related to neurotransmission and cell adhesion were altered in the brain of Crmp4-KO mice

295 unexpectedly, that GPI-anchored MMPs promote cell adhesion when they are rendered inactive.

296 including proliferation, migration, and cell-cell adhesion, which are all requisite for angiogenesis.

297 the blood-brain barrier involve endothelial cell adhesion, which is linked to cytoskeletal dynamics.

298 es between embryonic implantation and cancer cell adhesion, which suggests that abortifacients may be

299 Btbd7 promotes loss of E-cadherin from cell-cell adhesions with enhanced migration and transient cel

300 Selective inhibition of cell adhesion, wound healing, and invasion are demonstra