ライフサイエンスコーパス: cell-cell adhesion

1 t of the desmosome and known for its role in cell-cell adhesion.

2 egulation of actin cytoskeleton dynamics and cell-cell adhesion.

3 feature of compact tissues held together by cell-cell adhesion.

4 gher levels of cortical F-actin and enhanced cell-cell adhesion.

5 increased cytoskeletal tension and impaired cell-cell adhesion.

6 in organization and membrane dynamics during cell-cell adhesion.

7 domains of CDH23 and is predicted to impair cell-cell adhesion.

8 seems to control CdGAP residence at sites of cell-cell adhesion.

9 g the bimolecular interactions that maintain cell-cell adhesion.

10 ires its partner protein TraB to function in cell-cell adhesion.

11 d membrane dynamics during initial stages of cell-cell adhesion.

12 nt concentrations while not requiring strong cell-cell adhesion.

13 isoform switching and associated changes in cell-cell adhesion.

14 d E-cadherin at junctions and a weakening of cell-cell adhesion.

15 al collagen and enhanced E-cadherin-mediated cell-cell adhesion.

16 ell-to-cell variation in key parameters like cell-cell adhesion.

17 ll death or interfere with cadherin-mediated cell-cell adhesion.

18 dynamics, as well as substrate-mediated and cell-cell adhesion.

19 ht to mimic the CCC are sufficient to induce cell-cell adhesion.

20 dimer alphaE-catenin are required for strong cell-cell adhesion.

21 n-based protrusions that are specialized for cell-cell adhesion.

22 nhancing cell-matrix adhesion and decreasing cell-cell adhesion.

23 il-mediated Colo-205 apoptosis and inhibited cell-cell adhesion.

24 energy, actin cytoskeleton organization, and cell-cell adhesion.

25 ting a prominent role for CdiA-BamA mediated cell-cell adhesion.

26 ts keratinocytes from PV IgG-induced loss of cell-cell adhesion.

27 se activities, and the development of strong cell-cell adhesion.

28 cal for establishing cell wall integrity and cell-cell adhesion.

29 transition of cells from migration to strong cell-cell adhesion.

30 Par proteins, Wnt/PCP signaling pathway, and cell-cell adhesion.

31 ony, matrix dimensionality and softness, and cell-cell adhesion.

32 moglein 3 (Dsg3) and compromise keratinocyte cell-cell adhesion.

33 cell elongation requires E-cadherin-mediated cell-cell adhesion.

34 din-Darby canine kidney mammalian epithelial cell-cell adhesion.

35 120-catenin isoform 1A phenotype and reduced cell-cell adhesion.

36 e positioning with shape changes to maintain cell-cell adhesion.

37 nin complex and coordinate cadherin-mediated cell-cell adhesion.

38 cells lose polarity and E-cadherin-mediated cell-cell adhesion.

39 adherin SPRY motifs that are not involved in cell-cell adhesion.

40 t increases membrane E-cadherin and restores cell-cell adhesion.

41 tomyosin cytoskeleton and cell expansion via cell-cell adhesion.

42 lity of three-dimensional models in studying cell-cell adhesion.

43 strate adhesion dominate over those favoring cell-cell adhesion.

44 substrate-based motility be coordinated with cell-cell adhesion.

45 TPase activity and regulation, apoptosis and cell-cell adhesion.

46 s and TJs that is fundamental for epithelial cell-cell adhesion.

47 rane proteins that mediate calcium-dependent cell-cell adhesion.

48 cells and the increased Ca(2+)-cross linked cell-cell adhesion.

49 of mesenchymal phenotype and an increase in cell-cell adhesion.

50 n low-affinity homophilic bonds that promote cell-cell adhesion.

51 ene encodes a cell wall protein that imparts cell-cell adhesion.

52 tion, protein-carbohydrate interactions, and cell-cell adhesion.

53 erin cytosolic tail and thereby localizes at cell-cell adhesions.

54 rin and a reduction in alpha/beta-catenin at cell-cell adhesions.

55 tion, but not the maintenance of established cell-cell adhesions.

56 uired mechanotransduction through E-cadherin cell-cell adhesions.

57 d retractions (motility cycles) aided by the cell-cell adhesions.

58 m size, bulk cell stiffness and stiffness of cell-cell adhesions.

59 ibrillogenesis to the tissue surface lacking cell-cell adhesions.

60 ilopodia and membrane ruffles and at nascent cell-cell adhesions.

61 on of the membrane cortical cytoskeleton and cell-cell adhesions.

62 be altered by modulating the cell-matrix and cell-cell adhesions.

63 ctomyosin interactions, membrane tension, or cell-cell adhesions.

64 nd plakophilin-3 (PKP3), and are involved in cell-cell adhesions.

65 Here, we focus on epithelial cell-cell adhesion, a critical but understudied process

66 sion complex is the central component of the cell-cell adhesion adherens junctions that transmit mech

67 n which zinc plays a dual role in activating cell-cell adhesion: adsorption of zinc ions to the bacte

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

69 mbrane zippers, indicative of involvement in cell-cell adhesion and actin polymerization-dependent pr

70 ment is achieved through the modification of cell-cell adhesion and actomyosin-based contractility, w

71 Heterotypic cell-cell adhesion and aggregation mediate vaso-occlusiv

72 which cells lose epithelial traits, such as cell-cell adhesion and apico-basal polarity, and acquire

73 mophilic dimerization, regulates endothelial cell-cell adhesion and barrier function.

74 lexes are multiprotein subunits that promote cell-cell adhesion and barrier integrity.

75 the physiological regulation of keratinocyte cell-cell adhesion and blister development.

76 but poorly understood changes in epithelial cell-cell adhesion and cell motility.

77 w study upends the clear distinction between cell-cell adhesion and cell-matrix adhesion by showing t

78 Loss of cell-cell adhesion and chromosomal instability are cardi

79 relative contributions of osmotic pressure, cell-cell adhesion and cortical stiffness to mitotic rou

80 ions (AJs) is essential for the formation of cell-cell adhesion and epithelium integrity; however, st

81 PCs emerges as a novel mechanism to modulate cell-cell adhesion and fate allocation.

82 odified with S-GlcNAc are mainly involved in cell-cell adhesion and gene expression.

83 We model homotypic cell-cell adhesion and heterotypic cell-basement membran

84 , and microorganisms play important roles in cell-cell adhesion and host-pathogen interaction.

85 requiring the coordination of cadherin-based cell-cell adhesion and integrin-based cell migration.

86 ane receptor that mediates calcium-dependent cell-cell adhesion and is a major component of adhesive

87 /beta-catenin signaling pathway, its role in cell-cell adhesion and liver function, and the cell type

88 in.alpha-catenin complex mediates homophilic cell-cell adhesion and mechanically couples the actin cy

89 by disrupting long neural genes involved in cell-cell adhesion and migration.

90 ing network that guides spindle positioning, cell-cell adhesion and mitotic fidelity.

91 ligands have been associated with regulating cell-cell adhesion and motility, and thus have a critica

92 ells demonstrated diminished cell spreading, cell-cell adhesion and motility.

93 Both cell-cell adhesion and oriented cell division play promi

94 n/smooth muscle alpha actin; thus, mediating cell-cell adhesion and permeability.

95 creases Rac1 activity, which disrupts normal cell-cell adhesion and promotes invasion.

96 eversed the effects of Galpha13 knockdown on cell-cell adhesion and proteolytic invasion in three-dim

97 eversed the effects of Galpha13 knockdown on cell-cell adhesion and proteolytic invasion in three-dim

98 tional transmembrane molecule that regulates cell-cell adhesion and receptor-mediated endocytosis, al

99 %, respectively, reflecting a loss of normal cell-cell adhesion and signalling between axons and olig

100 ased IL-8 secretion by stromal cells through cell-cell adhesion and soluble factors.

101 enesis requires dynamic coordination between cell-cell adhesion and the cytoskeleton to allow cells t

102 ood cells, stromal inflammation, and loss of cell-cell adhesion and tissue architecture all contribut

103 and follower cells migrate while maintaining cell-cell adhesion and tissue polarity.

104 Whereas the regulation of beta-catenin in cell-cell adhesion and Wnt signaling are well understood

105 al beta-catenin, with critical roles in both cell-cell adhesion and Wnt-signaling pathways, was among

106 ar matrix (ECM) accompanied by a decrease in cell-cell adhesion and/or Rho family of small GTPase act

107 The formation of tightly controlled cell-cell adhesions and cell-matrix junctions between le

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

109 migratory states, regulated by differential cell-cell adhesions and protrusive activities to drive p

110 To heal, migrating tissues must form cell-cell adhesions and reorganize from the front-rear p

111 ant matrix, hESCs accumulate beta-catenin at cell-cell adhesions and show enhanced Wnt-dependent meso

112 Extrusion depends on E-cadherin-based cell-cell adhesions and signaling to the actin-myosin cy

113 alpha-Catenins are important mediators of cell-cell adhesion, and alphaT-catenin is predominantly

114 l-water fractions (MWFs) increase cell size, cell-cell adhesion, and cell death.

115 nctions including proliferation, metabolism, cell-cell adhesion, and cell migration.

116 The interplay between cell softness, cell-cell adhesion, and contact inhibition of locomotion

117 esulted in loss of cortical F-actin, reduced cell-cell adhesion, and disrupted localization of adhesi

118 n pattern, reduced proliferation, normalized cell-cell adhesion, and formation of crypts in tissue cu

119 cytes in epidermis and mucous membranes lose cell-cell adhesion, and in pemphigoid, the basal keratin

120 Fatl is involved in local cell alignment and cell-cell adhesion, and that reduction of HyFatl leads t

121 on the coordinated action of actin networks, cell-cell adhesions, and cell-extracellular matrix (ECM)

122 hat Mpp5a- and Rab11a-mediated resolution of cell-cell adhesions are both necessary for midline lumen

123 proper cellular organization and epithelial cell-cell adhesion as part of a program related to the e

124 Column formation requires cell-cell adhesion, as reducing cadherin binding via che

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

126 expression also supported proliferation and cell-cell adhesion at 24 h, and by 4 days colonies of Oc

127 haT-catenin and how alphaT-catenin regulates cell-cell adhesion at the cardiomyocyte ICD.

128 suggests a wider prevalence of heterophilic cell-cell adhesion-based ECD regulation during animal mo

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

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

131 assemblies at the cell surface and programed cell-cell adhesion between homotypic and heterotypic cel

132 in knockdown reversed Galpha13 siRNA-induced cell-cell adhesion but failed to reverse the effect of G

133 nb1(DM/loxp) mutants, which maintain partial cell-cell adhesion but not the transcription regulation

134 w that p120-catenin (p120) not only controls cell-cell adhesion, but also acts as a critical regulato

135 Cadherins mediate cell-cell adhesion by forming trans-interactions.

136 criptional target of Hh signaling to control cell-cell adhesion by negative regulation of E-cadherin

137 protein p120 catenin aids in maintenance of cell-cell adhesion by regulating E-cadherin stability in

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

139 estion of how cells that have down-regulated cell-cell adhesions can migrate collectively.

140 rtical tension reaches a critical threshold, cell-cell adhesion cannot be sustained during mitotic en

141 Moreover, loss of cell-cell adhesion caused up-regulation of cell-ECM adhe

142 ore, DUSP23 knockdown produced "zipper-like" cell-cell adhesions, caused defects in transmission of p

143 in receptors have a well-established role in cell-cell adhesion, cell polarization and differentiatio

144 g nervous system development, proliferation, cell-cell adhesion, cell spreading, and cellular differe

145 the extracellular matrix (ECM), cell-ECM and cell-cell adhesion complexes influence metabolic pathway

146 s lack components of the Wnt/PCP pathway and cell-cell adhesion complexes raising the question if cte

147 Adherens Junctions (AJs) are cell-cell adhesion complexes that sense and propagate me

148 alpha-Catenin links cell-cell adhesion complexes to the actin cytoskeleton,

149 urce for the study of mechanotransduction in cell-cell adhesions [corrected].

150 Cell-cell adhesion couples the contractile cortices of e

151 at in the absence of the protein, there is a cell-cell adhesion defect, particularly when cells are s

152 urface during cell separation and augmenting cell-cell adhesion does not impede detachment.

153 odeficient (3S>A) E-cadherin exhibit minimal cell-cell adhesion due to enhanced endocytosis and degra

154 s) whose down-regulation disrupts epithelial cell-cell adhesion during collective migration.

155 ococcus aureus surface protein SasG promotes cell-cell adhesion during the accumulation phase of biof

156 Failure to disassemble myocyte cell-cell adhesions during cardiac outflow tract develop

157 ght the central role of forces in regulating cell-cell adhesions during collective motility.

158 nd buds, where it enhances cell motility and cell-cell adhesion dynamics.

159 e been shown to influence hormone signaling, cell-cell adhesion, epithelial-to-mesenchymal transition

160 hymal transition (EMT) epithelial cells lose cell-cell adhesion, exhibit morphological changes, and u

161 Cells engaged in cell-cell adhesion expressed a high MW-modified form of

162 on patterns on microarray analysis including cell-cell adhesion factors and cytoskeletal and rho-GTPa

163 ted real-time actin assembly during daughter cell-cell adhesion formation in human breast epithelial

164 identified a new role for Cx50 that mediates cell-cell adhesion function.

165 clude that re-expression of APC restores the cell-cell adhesion gene and posttranscriptional regulato

166 also leads to reduced expression of several cell-cell adhesion genes (e.g., CDH1, VCL, CTNNA1), poss

167 ts of full-length, wild-type APC (fl-APC) on cell-cell adhesion genes and p120-catenin isoform switch

168 nt and cell-matrix adhesion genes but not in cell-cell adhesion genes.

169 consistent with down-regulated expression of cell-cell adhesion genes.

170 A feedback between cell density, CIL, and cell-cell adhesion gives rise to a linear relationship b

171 E-cadherin, a cell-cell adhesion glycoprotein, is frequently downregul

172 ween the internal cell polarization, CIL and cell-cell adhesion governs the collision outcome.

173 ast, isolated cells, or cells with disrupted cell-cell adhesions had nuclei with curved apical surfac

174 te within a cell aggregate, and differential cell-cell adhesion has been proposed to explain this beh

175 ses influence endothelial cell migration and cell-cell adhesion; however it is not known whether they

176 Cell aggregation depends on cell-cell adhesion; however, no rigorous approach exists

177 required specifically for cadherin-dependent cell-cell adhesion identified an Elmo-Dock complex.

178 However, how Thy-1 supports cell-cell adhesion in a dynamic mechanical environment i

179 catenin delta-1 S268, which in turn mediated cell-cell adhesion in astrocytes.

180 ances affinity for beta-catenin and promotes cell-cell adhesion in cell culture systems, but its impo

181 fects: decrease in filopodia and compromised cell-cell adhesion in cells migrating as a sheet.

182 Desmosomal cadherins mediate cell-cell adhesion in epithelial tissues and have been k

183 Aquaporins differentially regulate cell-cell adhesion in MDCK cells.

184 d by the microenvironment and on the role of cell-cell adhesion in mechanical and behavioral coupling

185 ns via the IQGAP1-Rac1 pathway to strengthen cell-cell adhesion in normal adult crypt stem cells and

186 clear positioning, extracellular matrix, and cell-cell adhesion in shaping Drosophila wing imaginal d

187 estes)-catenin, a critical factor regulating cell-cell adhesion in the heart, directly couples the ca

188 bulin superfamily glycoproteins that mediate cell-cell adhesion in vertebrate tissues.

189 se targeting genes with predicted effects on cell-cell adhesion, including sialophorin (SPN).

190 represses cell polarization and integrity of cell-cell adhesion, independently of its impact on beta-

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

192 ms steering nascent actin polymerization for cell-cell adhesion initiation are not well understood.

193 s novel screen eliminated Ca(2+)-independent cell-cell adhesion, integrin-based adhesion, cell spread

194 se a 3D cell-based simulation with realistic cell-cell adhesion, interaction forces, and chemotaxis.

195 Cell-cell adhesion is a key mechanism to control tissue

196 If cell-cell adhesion is absent, and the cluster cohesion i

197 Cadherin-mediated cell-cell adhesion is actin-dependent, but the precise r

198 Cell-cell adhesion is central to morphogenesis and maint

199 In cancer, cell-cell adhesion is compromised and is associated with

200 Here we show that loss of cell-cell adhesion is correlated with inactivation of RA

201 hat a balance between cell contractility and cell-cell adhesion is crucial for promoting basally orie

202 Cell-cell adhesion is essential for tissue growth and mu

203 The regulation of cell-cell adhesion is important in cell motility, tissue

204 Finally, our data suggest that cell-cell adhesion is insensitive to E-cadherin recyclin

205 but the precise role of actin in maintaining cell-cell adhesion is not fully understood.

206 We found that the level of cell-cell adhesion is precisely regulated by internaliza

207 During EMT cell-cell adhesion is reduced allowing cells to dissocia

208 Cadherin-mediated cell-cell adhesion is required for epithelial tissue int

209 Plasticity of epithelial cell-cell adhesion is vital in epithelial homeostasis an

210 ow epithelial cells regulate cell-matrix and cell-cell adhesions is essential to understand key event

211 such as type I and II interferon signaling, cell-cell adhesion, leukocyte chemotaxis, and angiogenes

212 ctional connection between cell polarity and cell-cell adhesion machineries in mammalian cells.

213 e4 and that these proteases jointly regulate cell-cell adhesion mediated by E-cadherin processing.

214 ion pathways (e.g., trans-endocytosis) using cell-cell adhesion, membrane trafficking, and membrane r

215 e created and stabilized using hydrogels and cell-cell adhesion methods.

216 on pattern with the epithelial cell-specific cell-cell adhesion molecule E-cadherin in the dental epi

217 al cells), we show that IFs downregulate the cell-cell adhesion molecule E-cadherin on non-tumorigeni

218 ABSTRACT: N-cadherin is the major cell-cell adhesion molecule in vascular smooth muscle ce

219 E-cadherin is a cell-cell adhesion molecule that acts as a suppressor of

220 E-cadherin is a major homophilic cell-cell adhesion molecule that inhibits motility of in

221 Although Pcdh19 is known to be a homophilic cell-cell adhesion molecule, how its mutations bring abo

222 er, limited knowledge exists on the relevant cell-cell adhesion molecules involved in physiological e

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

224 vior of muscle relied upon the same suite of cell-cell adhesion molecules that functioned in the endo

225 though classic EMT hallmarks include loss of cell-cell adhesions, morphology changes, and increased i

226 5 proteins, associated with protein folding, cell-cell adhesion, NADH dehydrogenase activity, ATP-bin

227 Desmosomes are cell-cell adhesions necessary for the maintenance of tis

228 o cellular mechanisms leading to the loss of cell-cell adhesion, new ideas were shared in the field o

229 efense, telomere maintenance, signaling, and cell-cell adhesion.Objectives: To improve our understand

230 11-DeltaAmot) did not abolish Cad11-mediated cell-cell adhesion of mouse L cells, but significantly r

231 ellular basis of this phenotype is defective cell-cell adhesions of developing germ cells to Sertoli

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

233 ellular matrix (ECM) and E-cadherin-mediated cell-cell adhesions on the orthogonal, lateral surfaces

234 lower expression of subnetworks involved in cell-cell adhesion or cell death than did TCL1 leukemia

235 ur simulations predicted that either reduced cell-cell adhesion or reduced contact inhibition of prol

236 hich may account for the cytoskeleton, polar cell-cell adhesion, or the extracellular matrix in anima

237 at plasma membrane (P = 7.64 x 10(-)(3)(0)), cell-cell adhesion (P = 2.42 x 10(-)(1)(8)), synaptic tr

238 ransport (P-value=1.36 x 10(-11)) and neuron cell-cell adhesion (P-value=1.48 x 10(-13)).

239 biology studies have shown that cell-ECM and cell-cell adhesions participate in mechanosensing to tra

240 and highly applicable software for profiling cell-cell adhesion phenotypes and facilitate studies on

241 Cell-cell adhesion plays a key role in the collective mi

242 n signaling pathway, and E-cadherin-mediated cell-cell adhesion plays pivotal roles in determining th

243 ailable to understand if deregulation of the cell-cell adhesion programme is important in tumour form

244 ntegrity and support the deregulation of the cell-cell adhesion programme,which plays a critical role

245 tions between the different cases, including cell-cell adhesion, propulsion strength, and the rates o

246 inding by the human version of the essential cell-cell adhesion protein alphaE-catenin but not its ho

247 Cell-cell adhesion protein alphaE-catenin inhibits skin

248 We demonstrate that the cell-cell adhesion protein E-cadherin and the desmosome

249 Here, we demonstrate that the cell-cell adhesion protein E-cadherin functions as an in

250 llmark of ILCs is the functional loss of the cell-cell adhesion protein E-cadherin.

251 EACAM1 is a widely expressed multifunctional cell-cell adhesion protein reported to serve as a poor p

252 Downregulating the cell-cell adhesion protein, E-cadherin, enables MCF-10A

253 acellular region of E-cadherin, an essential cell-cell adhesion protein.

254 Cell-cell adhesion proteins and antiproteases were reduc

255 Classical cadherin cell-cell adhesion proteins are essential for the format

256 Classical cadherin Ca(2+)-dependent cell-cell adhesion proteins play key roles in embryogene

257 linkages between the CCARPs and other known cell-cell adhesion proteins, including hits from recent

258 s of one novel CCARP which links to multiple cell-cell adhesion proteins, the phosphatase DUSP23, rev

259 y of the cadherin family of Ca(2+)-dependent cell-cell adhesion proteins, which play essential roles

260 nd alpha-actinin-4 decreases the strength of cell-cell adhesion, reduces the monolayer permeability b

261 w that cell-expansive forces of heterophilic cell-cell adhesion regulate ECD: higher cell-cell adhesi

262 Force transduction at cell-cell adhesions regulates tissue development, mainte

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

264 We previously identified 27 candidate cell-cell adhesion regulatory proteins (CCARPs) whose do

265 Analysis of cell-cell adhesion-related proteins in SW480+APC cells r

266 s, yet FGF functions such as cell-matrix and cell-cell adhesion remained unaffected, though these act

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

268 ns unique to multicellular organisms such as cell-cell adhesion, signaling, immune defense and develo

269 fication and NHE1 overexpression both reduce cell-cell adhesion strength, indicated by reduced maximu

270 l-substrate adhesion and decreased homotypic cell-cell adhesion strength.

271 main but not N-cadherin-dependent homophilic cell-cell adhesion, suggesting that other N-cadherin-bin

272 division, daughter chondrocytes establish a cell-cell adhesion surface enriched in cadherins and bet

273 ng morphogenesis to regulate cell-matrix and cell-cell adhesions that are required for cell patternin

274 ferentiation in addition to participating in cell-cell adhesion, the role of Dsg1 in aiding different

275 adherin plays a critical role in endothelial cell-cell adhesion, thereby controlling endothelial perm

276 ants in the EC4-EC5 domains have a defect in cell-cell adhesion; this defect includes impaired bindin

277 ated with morphologic elongation and loss of cell-cell adhesions, though little is known about how it

278 ts typical of the epithelial lineage such as cell-cell adhesion, tight junctions and markers of diffe

279 ed that Axl is involved in the disruption of cell-cell adhesion to allow invasion and chemotherapy re

280 yed nanobodies that mediate antigen-specific cell-cell adhesion to effectively overcome the barrier t

281 nsional mesomimetic cultures showed enhanced cell-cell adhesion to the lipid-loaded mesothelium.

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

283 e in this process by coupling cadherin-based cell-cell adhesion together with actomyosin contractilit

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

285 hat EphB4 controls the function of caveolae, cell-cell adhesion under mechanical stress and lipid tra

286 Mutation of the MUR4 gene led to abnormal cell-cell adhesion under salt stress.

287 l force measurements show that SasG mediates cell-cell adhesion via specific Zn(2+)-dependent homophi

288 In vitro experiments confirmed that cell-cell adhesion was reduced and proliferation was inc

289 es between single cells, and a novel mode of cell-cell adhesion was uncovered: amyloid-like interacti

290 example, C. elegans HMP-2 functions only in cell-cell adhesion, whereas SYS-1 mediates transcription

291 reased the expression of genes implicated in cell-cell adhesion, whereas the expression of negative r

292 iors including proliferation, migration, and cell-cell adhesion, which are all requisite for angiogen

293 intercellular junction molecules increasing cell-cell adhesion with downregulation of Wnt and TGFbet

294 Sdks mediate cell-cell adhesion with homophilic specificity that unde

295 that Btbd7 promotes loss of E-cadherin from cell-cell adhesions with enhanced migration and transien

296 ed from impaired cell motility and defective cell-cell adhesion, with damaged cells additionally defe

297 omote tumor invasion through an influence on cell-cell adhesion within the tumor and highlight the im

298 ltifunctional protein with critical roles in cell-cell adhesion, Wnt signaling, and the centrosome cy

299 h frequently mutated genes included those of cell-cell adhesion/Wnt/Hippo in 76%, oxidative stress re

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