ライフサイエンスコーパス: cell-cell adhesion

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

27 required subsequently for the maintenance of cell-cell adhesion.

28 een O-mannosyl glycans and cadherin-mediated cell-cell adhesion.

29 njunction with disruption of cell-matrix and cell-cell adhesion.

30 increased cytoskeletal tension and impaired cell-cell adhesion.

31 brane expression of DSG1, leading to loss of cell-cell adhesion.

32 with a number of diseases due to failures in cell-cell adhesion.

33 cell-cell junctions 4 h after initiation of cell-cell adhesion.

34 tional cell migration, pathogen sensing, and cell-cell adhesion.

35 including catenins and vinculin, at sites of cell-cell adhesion.

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

37 amily, mediates calcium-dependent homophilic cell-cell adhesion.

38 atenin, suggesting the implication of AhR in cell-cell adhesion.

39 and associated proteins play a vital role in cell-cell adhesion.

40 ith changes in cytoskeletal organization and cell-cell adhesion.

41 nd a new role of talin in cadherin-dependent cell-cell adhesion.

42 herin-based adherens junction that regulates cell-cell adhesion.

43 asmic partners, catenins, mediate epithelial cell-cell adhesion.

44 leton is tightly regulated to achieve proper cell-cell adhesion.

45 saics are speculated to require differential cell-cell adhesion.

46 Initially, loss-of-STMN1 compromises cell-cell adhesion.

47 d by Scrib and elicited by cadherin-mediated cell-cell adhesion.

48 n, where Scrib strengthens cadherin-mediated cell-cell adhesion.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 itiate migration by promoting the release of cell-cell adhesions.

66 1c KD reduced the stability of E-cadherin at cell-cell adhesions.

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

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

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

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

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

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

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

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

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

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

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

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

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

80 , show association with cell-cell signaling, cell-cell adhesion and cell proliferation, and have a no

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

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

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

84 suggest that genes involved in host defense, cell-cell adhesion and DNA repair contribute to risk of

85 ions about cadherin's biological function in cell-cell adhesion and downstream signaling.

86 have found that JNK is required to maintain cell-cell adhesion and establish parallel microtubule ar

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

88 on factor Cbf12p, which is known to increase cell-cell adhesion and flocculation when overexpressed.

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

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

91 ndent N-cadherin shedding leads to increased cell-cell adhesion and inhibition of cell motility.

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

93 throid specification, rapid cell growth, and cell-cell adhesion and interaction.

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

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

96 ndent apical ECM organization contributes to cell-cell adhesion and may modulate epithelial junction

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

98 fferentiation, as well as dynamic changes in cell-cell adhesion and migration.

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

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

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

102 In vitro assays show that NEGR1 promotes cell-cell adhesion and neurite growth of hypothalamic ne

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

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

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

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

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

108 at Rack1, partly by inhibiting Src, promotes cell-cell adhesion and reduces the invasive potential of

109 ural cell adhesion molecule (NCAM) modulates cell-cell adhesion and signaling, is required for proper

110 %, respectively, reflecting a loss of normal cell-cell adhesion and signalling between axons and olig

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

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

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

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

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

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

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

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

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

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

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

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

123 f thin actin bundles associated with nascent cell-cell adhesions and that this is required to sustain

124 Cell-cell adhesions and the cytoskeletons play important

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

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

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

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

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

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

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

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

133 ng site is necessary for its localization to cell-cell adhesions, and fluorescence recovery after pho

134 ent closely correlated with the formation of cell-cell adhesions, and this fragment localized to cadh

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

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

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

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

139 y a direct molecular link between changes in cell-cell adhesion at epithelial edges and induction of

140 Mutual, homophilic cell-cell adhesion between epithelial cells is required

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

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

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

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

145 and vinculin-binding protein that regulates cell-cell adhesion by interacting with cadherin adhesion

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

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

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

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

150 Because cell-cell adhesions cannot be measured directly, we use

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

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

153 Here we assess the function of ARHGAP21 in cell-cell adhesion, cell migration, and scattering.

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

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

156 processes, such as proliferation, migration, cell-cell adhesion, cell-extracellular matrix (matrix) a

157 Rap1 is a small GTPase regulating cell-cell adhesion, cell-matrix adhesion, and actin rear

158 n of proteins is involved in immune defense, cell-cell adhesion, cellular recognition and pathogen bi

159 n epithelial cells, Par3 is localised to the cell-cell adhesion complex and is important in the defin

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

161 Cell-cell adhesion couples the contractile cortices of e

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

163 BMK1 elevation augmented E-cadherin-mediated cell-cell adhesion, downregulated mesenchymal markers, a

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

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

166 volutionary conserved mechanisms to regulate cell-cell adhesion during development and cancer.

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

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

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

170 Upon completion of cell-cell adhesion, Elmo2 and Dock1 no longer localize t

171 RbmA participates in the early cell-cell adhesion events and is found throughout the bi

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

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

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

175 ellular domains of Crb2a and Crb2b mediate a cell-cell adhesion function, which plays an essential ro

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

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

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

179 Here, we identify the essential cell-cell adhesion glycoprotein epithelial (E)-cadherin

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

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

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

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

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

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

186 ingle cells, suggesting that the presence of cell-cell adhesion improves 3D cell migration.

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

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

189 th increased alpha5 localization at sites of cell-cell adhesion in breast cancer patients, while high

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

191 own to exhibit homophilic binding and confer cell-cell adhesion in cells including epithelial and can

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

193 al implications in the maintenance of proper cell-cell adhesion in epidermal stem cells.

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

195 at downregulation of FLCN leads to increased cell-cell adhesion in functional cell-based assays and d

196 The dynein-NCAM180 interaction also enhances cell-cell adhesion in heterologous cell assays.

197 he technique has been applied to investigate cell-cell adhesion in human epithelial cells.

198 and angiogenesis, and increase apoptosis and cell-cell adhesion in in vitro and in vivo experiments.

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

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

201 We also show that lowered cell-cell adhesion in the cleft region and increased cle

202 The role of cell-cell adhesion in the regulation of epithelial topol

203 sed stress fiber formation, cell-matrix, and cell-cell adhesion in the shRNARelB (shRelB) cells durin

204 gulate the levels of transcripts involved in cell-cell adhesion in this species.

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

206 Bdl induces homotypic cell-cell adhesion in vitro and mediates neurite-neurite

207 ntermediate filament retraction, and loss of cell-cell adhesion in vitro.

208 Finally, to examine the role of Flcn loss on cell-cell adhesion in vivo, we utilized keratin-14 cre-r

209 ork defines the importance of cadherin-based cell-cell adhesions in coordinating mechanical activity

210 on controls the formation and maintenance of cell-cell adhesions in epithelia.

211 rcalation that was associated with decreased cell-cell adhesion, in a similar manner to E-cadherin de

212 ells lacking ARHGAP21 expression show weaker cell-cell adhesions, increased cell migration, and a dim

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

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

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

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

217 Cell-cell adhesion is central to morphogenesis and maint

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

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

220 Although loss of cell-cell adhesion is key to breast cancer progression,

221 uch as epidermal growth factor (EGF) have on cell-cell adhesion is of interest in the study of cellul

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

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

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

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

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

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

228 A minimal physical model in which cell-cell adhesions modulate the physical cohesion betwe

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

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

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

232 N-cadherin is a cell-cell adhesion molecule that plays a role in breast

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

234 Cadherins are homophilic cell-cell adhesion molecules implicated in many fundamen

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

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

237 ment of genes implicated in axonal guidance, cell-cell adhesion, neuronal morphogenesis and different

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

239 11-DeltaAmot) did not abolish Cad11-mediated cell-cell adhesion of mouse L cells, but significantly r

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

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

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

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

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

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

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

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

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

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

250 expression of FLO11, a major determinant of cell-cell adhesion, produced diverse lineage-specific mu

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

252 Cell-cell adhesion protein alphaE-catenin inhibits skin

253 cytoskeleton and adherens junctions (AJs), a cell-cell adhesion protein complex associated with the a

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

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

256 l light-triggered switch in the Ca-dependent cell-cell adhesion protein E-cadherin, created using a m

257 through immunofluorescence labelling of the cell-cell adhesion protein E-cadherin.

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

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

260 Cell-cell adhesion proteins and antiproteases were reduc

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

262 Classical cadherin cell-cell adhesion proteins play key morphogenetic roles

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

264 Cadherins are Ca(2+)-dependent cell-cell adhesion proteins that maintain the structural

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

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

267 N-cadherin is a homotypic cell-cell adhesion receptor commonly overexpressed in tu

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

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

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

271 ion of tissue boundaries is dependent on the cell-cell adhesion/repulsion system that is required for

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

273 E-cadherin is normally involved in cell-cell adhesion, so it not surprising that individual

274 lows: cleft cell contractility, cleft region cell-cell adhesion strength, epithelial cell mitosis rat

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

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

277 te to transitions between cell migration and cell-cell adhesion that depend on remodeling the actin c

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

279 oGAP was identified as a key requirement for cell-cell adhesions that permit collective migration.

280 and function of tight junctions, specialized cell-cell adhesions that restrict water loss in the epid

281 ed signaling pathways that induce changes in cell-cell adhesion, the cytoskeleton, integrin function,

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

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

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

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

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

287 es in a feedback with cell contractility and cell-cell adhesion to regulate collective migration.

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

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

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

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

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

293 Ca(2+)-cross-linked pectin in these samples, cell-cell adhesion was still stronger than in the high-t

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

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

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

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

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

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

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