ライフサイエンスコーパス: adhesion

1 ved in their reorganization to sites of cell adhesion.

2 aining two tandem PDZ domains mediating cell adhesion.

3 the increased Ca(2+)-cross linked cell-cell adhesion.

4 esistin, which augments monocyte-endothelial adhesion.

5 th cell-spreading assays to investigate cell adhesion.

6 proteins influencing cellular integrity and adhesion.

7 -based system with significant anisotropy of adhesion.

8 g and intracellular pathways related to cell adhesion.

9 id fibronectin fibrillogenesis distal to the adhesion.

10 eolian vibration, enabling self-sustained PM adhesion.

11 tion, which does not increase in response to adhesion.

12 witching and associated changes in cell-cell adhesion.

13 functions of specific talin isoforms in cell adhesion.

14 rs, and impaired BCR signalling and cellular adhesion.

15 ulted in attenuated LFA-1-dependent cellular adhesion.

16 mpromised angiogenesis and enhanced monocyte adhesion.

17 layer spacing resulting from peptide-induced adhesion.

18 in cultured mouse podocytes compromises cell adhesion.

19 d N-WASP, but not pVASP, cortactin and focal adhesions.

20 tein vinculin, they do not form mature focal adhesions.

21 pport JUN as a therapeutic target to prevent adhesions.

22 diated FAK activation and signaling at focal adhesions.

23 ractile stress fibers that bind the discrete adhesions.

24 P-deficiency also impaired integrin-mediated adhesion accompanied by reduced traction forces exerted

25 n and material softening likely produce high adhesion across a range of relative humidity values.

26 hilst simultaneously releasing contralateral adhesions across the centre of the tissue.

27 criptional pathway triggered by loss of cell adhesion activates lysosomes in C. elegans epidermis dur

28 this pool of ceramide acutely regulates cell adhesion and cell migration pathways with weak connectio

29 tin plays an important role in intercellular adhesion and controlling the porosity of the wall.

30 by regulating the process of cell invasion, adhesion and epithelial-mesenchymal transition (EMT).

31 n complex on the organism with importance in adhesion and immune recognition.

32 rin alpha5 expression were enhanced but COL1 adhesion and integrin alpha2 expression were unchanged u

33 We also demonstrate that substrate adhesion and integrin localization are enhanced by mamma

34 bits biofilm formation by Nm, and impedes Nm adhesion and invasion of human airway cells.

35 topographic interactions to strengthen cell adhesion and large surface areas for grafting capture ag

36 with higher mechanical rigidity, better bio-adhesion and longer residence time than Poloxamer hydrog

37 gulated expression of genes involved in cell adhesion and markers of decidualisation.

38 w temperature (12 degrees C), both capillary adhesion and material softening likely produce high adhe

39 ame frequency independently facilitate focal adhesion and mechanosensing of stem cells, which are col

40 rols kidney salt homeostasis, also regulates adhesion and migration in CD4(+) T cells.

41 iophysical and functional changes including, adhesion and migration in EOC-derived fibroblasts that s

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

43 Integrin-ligand interaction mediates the adhesion and migration of many metazoan cells.

44 to assess immunophenotype, differentiation, adhesion and migration properties and cell signalling pa

45 r processes including the regulation of cell adhesion and migration.

46 ls enriched in proteins associated with cell adhesion and migration.

47 Changes in pathways associated with adhesion and molecular remodeling were also documented.

48 that WNK1 negatively regulates LFA1-mediated adhesion and positively regulates CXCL12-induced migrati

49 r activities, including migration, invasion, adhesion and proliferation.

50 ion, while RNAi knockdown of SEMA4C promotes adhesion and reduces cellular proliferation, colony form

51 ital microscopy showed decrease in leukocyte adhesion and rolling after ethanol consumption.

52 inculin regulates some aspects of neutrophil adhesion and spreading, it may be dispensable for beta2

53 lar mechanisms that govern astrocyte-synapse adhesions and how astrocyte contacts control synapse for

54 ell-cell and cell-extracellular matrix (ECM) adhesions and is modulated by cell tension and tissue-le

55 nd, more specifically, to the maintenance of adhesions and retraction fibers in mitosis [1-6], which

56 ptomic changes affecting cell motility, cell adhesion, and cytoskeleton organization.

57 velopmental gene involved in cell migration, adhesion, and morphogenesis.

58 can regulate cell proliferation, migration, adhesion, and remodeling of the extracellular matrix.

59 ubstances involve phagocytosis, endocytosis, adhesion, and signaling.

60 unctions in both actin filament turnover and adhesion, and the novel mechanistic insights substantial

61 xisting host cell heterogeneity in bacterial adhesion, and we find no evidence for significant hetero

62 and Rab11a-mediated resolution of cell-cell adhesions are both necessary for midline lumen opening a

63 Adhesions are fibrotic scars that form between abdominal

64 Postoperative adhesions are most common issues for almost any types of

65 Adhesions are the most common driver of long-term morbid

66 mors, however, is the need to modulate their adhesion as they detach from the tumor and migrate throu

67 involved in migration, chemotaxis, and cell adhesion as well as induction of a proinflammatory and p

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

69 sion complex but did exhibit intrinsic focal adhesion assembly as well as contractile differences tha

70 uch as myosin filament formation and nascent adhesion assembly, but not those requiring stable actomy

71 eart via transcriptional activation of focal adhesion assembly.

72 10 embryos exhibit transient oral epithelial adhesions at E13.5, which may delay shelf elevation.

73 a wider prevalence of heterophilic cell-cell adhesion-based ECD regulation during animal morphogenesi

74 cific chemistries are known to promote tight adhesion between adjacent membranes via the formation of

75 l homeostasis by strengthening intercellular adhesion between cells.

76 ips of brush border microvilli that mediates adhesion between neighboring protrusions.

77 100 pM could be measured by the differential adhesion between SCP and biochip surface, supported by a

78 ssel across the fovea with shadow effect and adhesions between the vitreous and the aberrant macroves

79 Our understanding of adhesion biology is limited, which explains the paucity

80 not entirely controlled by the interparticle adhesion, but that stiffness and inelasticity of the gra

81 orces, suggesting that these species mediate adhesion by chemical bridging.

82 asured eosinophil binding with a Sykes-Moore adhesion chamber.

83 Furthermore, the differential adhesion code is regulated by the sonic hedgehog morphog

84 tenin-mediated signaling to promote cellular adhesion/colonization and organoid formation by controll

85 border is controlled by the intermicrovillar adhesion complex (IMAC), a protocadherin-based complex f

86 ke protein 4 (CALML4) is a component of this adhesion complex and functions as a light chain for myos

87 expression of proteins involved in the focal adhesion complex but did exhibit intrinsic focal adhesio

88 Because the intermicrovillar adhesion complex is homologous to the myosin-7a (MYO7A)-

89 in HeLa cells, which do not normally produce adhesion complex proteins, this chimera trafficked to th

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

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

92 Integrin-based focal adhesion complexes link the glial membrane to the extrac

93 ponents of the Wnt/PCP pathway and cell-cell adhesion complexes raising the question if ctenophore ce

94 ently reinforces the mechanical stability of adhesion complexes.

95 RAP1 activation is required for cell-matrix adhesion confirmed by adhesion to fibronectin-coated pla

96 TGFbeta-induced LPP localization to cellular adhesions depended on SHCA.

97 First, we show that adhesions derive primarily from the visceral peritoneum,

98 Specifically, capillary adhesion dominates on hydrophilic substrates, and materi

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

100 important mechanism for fine-tuning cell-ECM adhesion during cell migration in development.

101 d adapter protein talin coordinates cell-ECM adhesion during melanoblast migration in vivo Specifical

102 -1B colocalized with beta1 integrin in focal adhesions during cell migration using confocal microscop

103 III effector TarP, which localized to focal adhesions during infection and when expressed ectopicall

104 trafficking to the plasma membrane and focal adhesion dynamics.

105 gle parameter, which combines the effects of adhesion, elasticity, and dissipation.

106 iring stable actomyosin bundles, e.g., focal adhesion elongation or migratory front-back polarization

107 ogical function, in terms of, e.g., cellular adhesion, endo/exocytosis, cellular uptake, and mechanos

108 egrin-mediated mechanotransduction and focal adhesion (FA) dynamics.

109 rately indicate the onset and propagation of adhesion failure to the evolution of piezo-resistivity i

110 knockdown of Rab18 reduces the size of focal adhesions (FAs) and influences their dynamics.

111 and showed that force distribution in focal adhesions (FAs) is off-centered and FA size-dependent.

112 -sequencing, we identify heterogeneity among adhesion fibroblasts, which is more pronounced at early

113 The maximum obtained adhesion force of a positively polarized PDA-modified AF

114 VSMC adhesion force to FN (+33%) and integrin alpha5 expressi

115 By directly measuring adhesion forces and preferences for three types of endog

116 s between hydrolyzed adsorbates and particle-adhesion forces, suggesting that these species mediate a

117 consistent with our clinical experience that adhesions form primarily following laparotomy rather tha

118 ls dynamic cellular processes, such as focal adhesion formation and turnover and cell division.

119 ould be applied intra-operatively to prevent adhesion formation could dramatically improve the lives

120 integrin alpha6beta4 exhibit increased focal adhesion formation, cell spreading, and traction-force g

121 GPR56, a member of the adhesion G protein-coupled receptor family, is abundantl

122 Adhesion G protein-coupled receptors (AGPCRs) are a thir

123 The experimental evidence that Adhesion G Protein-Coupled Receptors (aGPCRs) functional

124 The large and alternatively-spliced ECRs of adhesion G protein-coupled receptors (aGPCRs) have key f

125 re-expression of APC restores the cell-cell adhesion gene and posttranscriptional regulatory program

126 -length, wild-type APC (fl-APC) on cell-cell adhesion genes and p120-catenin isoform switching in SW4

127 Such fatigue-resistant adhesion has not been achieved between synthetic hydroge

128 ic model reveals the underlying mechanism of adhesion hysteresis and dynamic instability.

129 ace adhesion receptors mediating cell-matrix adhesion in animals.

130 Here, we investigate cell-substrate adhesion in Capsaspora owczarzaki, the closest unicellul

131 protrusive activity is required to maintain adhesion in confluent sheets of epithelial cells is not

132 importance of integrin-mediated cell-matrix adhesion in development of multicellular animals, it is

133 of EPHB2 prevented ethanol inhibition of L1 adhesion in NIH/3T3 cells.

134 Transition from cooperative to Langmuir adhesion in sfGFP-Car9 variants occurs in concert with a

135 we investigate the role of cadherin-mediated adhesion in the development of zebrafish ocular motor (s

136 e mechanisms that regulate integrin-mediated adhesion in vivo in melanoblasts are not well understood

137 mbrane in 10%, 7.5%, and 5% (P = .005), iris adhesions in 62.5%, 57.5%, and 20% (P = .02), iris stump

138 nt strengthens and stabilizes integrin-based adhesions in melanocytes, which impinges on their abilit

139 al analysis were mainly associated with cell adhesion, inflammatory response, and extracellular exoso

140 Cadherin-mediated cell-cell adhesion is actin-dependent, but the precise role of act

141 Here we show that loss of cell-cell adhesion is correlated with inactivation of RAP1 confirm

142 Precise regulation of integrin-mediated adhesion is important for many developmental migration e

143 el, can also swim in the bulk, where surface adhesion is impossible.

144 thelial inflammation and subsequent monocyte adhesion is KLF2 dependent.

145 ecise role of actin in maintaining cell-cell adhesion is not fully understood.

146 Biomimicry of such structured adhesion is regularly achieved by top-down lithography,

147 in to promote protrusions and migration when adhesion is spatially-gapped.

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

149 enerated fibroblast-specific inducible focal adhesion kinase (FAK) knockout (cKO) mice in a breast ca

150 HDAC5 tyrosine 642 phosphorylation by focal adhesion kinase (FAK), a HDAC5 post-translational modifi

151 horylated forms of paxillin (pPXN) and focal adhesion kinase (pFAK).

152 an ITGA2-dependent phosphorylation of focal adhesion kinase and mitogen-activated protein kinase pat

153 vertical displacement of paxillin and focal adhesion kinase from the signaling layer of focal adhesi

154 hibition of integrin signaling through focal adhesion kinase inhibition caused disruption of cellular

155 ansduction after injury with increased focal adhesion kinase signaling and nuclear translocation of t

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

157 ype I and II interferon signaling, cell-cell adhesion, leukocyte chemotaxis, and angiogenesis.

158 ein product is a critical component of focal adhesions linking signaling between the extracellular ma

159 Composed of protocadherins CDHR2 and CDHR5, adhesion links are stabilized at the tips by a cytoplasm

160 media, can strongly alter such properties as adhesion, lubrication, friction and corrosion, and is im

161 ed for; pathways-in-cancer (including; focal adhesion, MAPK signaling, PI3K-Akt-mTOR signaling, p53 s

162 drophilic self-assembled monolayers, and for adhesion measurements of bacteria in dependence of alter

163 model in which differences in intercellular adhesion mediate cell sorting.

164 ken together, our results show that cell-ECM adhesions mediate coupling between the substrate and MSF

165 a surrogate for neutralization of intestinal adhesion mediated by CfaE.

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

167 l-surface integrin receptors to promote cell adhesion, migration, and proliferation.

168 omposition, structure, self-association, and adhesion modality in a panel of variants of the Car9 sil

169 rs, we provide evidence for the differential adhesion model in which differences in intercellular adh

170 of the carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family, which interact with m

171 E-selectin and intercellular adhesion molecule (ICAM)-1 are biomarkers of endothelial

172 udes selected residues from an intercellular adhesion molecule (ICAM)-like motif shared between the S

173 We identified Neural Cell Adhesion Molecule (NCAM1) as a potential ZIKV receptor a

174 ctions in vivo, which includes neuronal cell adhesion molecule (NRCAM).

175 other rhinoviruses, which bind intercellular adhesion molecule 1 receptors via a capsid protein VP1-s

176 ctor alpha, caspase-1 (CASP1), intercellular adhesion molecule 1, IL-10, heme oxygenase 1 hypoxia-ind

177 (Flk1, Tal1/Scl1, platelet endothelial cell adhesion molecule 1, vascular endothelial-cadherin, and

178 inal epithelial barrier function, junctional adhesion molecule A knockout mice, F11r(-/-) .

179 SIGLEC12, as well as the CD2 ligand and cell adhesion molecule CD58, all of which may be involved in

180 Cell adhesion molecule close homolog of L1 (CHL1) and the dop

181 The cell adhesion molecule E-cadherin is a major component of adh

182 one-dominant species, we identified the cell-adhesion molecule ELFN2 to be pivotal for the functional

183 Proteolytic cleavage of the cell adhesion molecule L1 (L1) in brain tissue and in culture

184 n autism-associated mutation in the synaptic adhesion molecule Nlgn3 results in impaired oxytocin sig

185 rst hiPSC-derived BBB model that displays an adhesion molecule phenotype that is suitable for the stu

186 lls had higher levels of ICAM (intercellular adhesion molecule)-1 and TF expression following TNF (tu

187 erminals functions in synergy with a related adhesion molecule, ELFN1, and their concerted interplay

188 tercellular adhesion molecule, vascular cell adhesion molecule, thrombomodulin) and inflammatory biom

189 Willebrand factor, E-selectin, intercellular adhesion molecule, vascular cell adhesion molecule, thro

190 Intercellular adhesion molecule-1 (ICAM-1) expressing neutrophils prod

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

192 Soluble intercellular adhesion molecule-1 (sICAM1) was measured in the plasma

193 0 mmol/L; P = 0.021), and intercellular cell adhesion molecule-1 (WA: 153.9 ng/mL; CB: 159.4 ng/mL; P

194 ts after LIGHT stimulation via intercellular adhesion molecule-1.

195 st commonly in the brain, on the neural cell adhesion molecule.

196 egulate carcinoembryonic antigenrelated cell adhesion molecules (CEACAMs) on the surface of small int

197 Down syndrome cell adhesion molecules (dscam and dscaml1) are essential reg

198 identified the immunoglobulin family of cell adhesion molecules (IgCAMs) as direct substrates, with D

199 vestigations into TJ proteins and junctional adhesion molecules (JAM) in cancer suggested a tumor-sup

200 ct interactions are collectively called cell adhesion molecules and are divided into four major group

201 ound a strong positive correlation with cell adhesion molecules and IFN response pathways and a stron

202 f cones and illustrate how interplay between adhesion molecules and postsynaptic transmitter receptor

203 of nutrient transporters, down-regulation of adhesion molecules and tumor suppressing phosphatases, a

204 thermore, it is appreciated that endothelial adhesion molecules are heavily N-glycosylated, but beyon

205 ate differences in chemokines, cytokines, or adhesion molecules associated with monocyte recruitment,

206 m was associated with elevated levels of the adhesion molecules ICAM and VCAM and the pattern-recogni

207 yeloid leukemia (bcCML) and identify several adhesion molecules that are preferentially expressed in

208 ins (NLGNs) are a class of postsynaptic cell adhesion molecules that interact with presynaptic neurex

209 beta2 integrins are critical adhesion molecules that regulate a number of neutrophil

210 ing from extracellular matrix components and adhesion molecules to chemokines and growth factors.

211 transmembrane (LRRTM) proteins are synaptic adhesion molecules with roles in synapse formation and s

212 eased HEVs, upregulated chemokines, and cell adhesion molecules, and led to greater numbers of Tregs

213 ty ligands specific for the endothelial cell adhesion molecules, PECAM-1 (CD31) and ICAM-1 (CD54).

214 ribe recent therapeutic approaches targeting adhesion molecules.

215 an extracellular substrate through specific adhesion molecules.

216 tripeptide arginyl-glycyl-aspartic acid cell adhesion motif RGD, which can be used as coating, but ca

217 lomere maintenance, signaling, and cell-cell adhesion.Objectives: To improve our understanding of fac

218 tion in cultured platelets and decreased the adhesion of Abeta-activated platelets to injured carotid

219 low concentrations of sphingosine prevented adhesion of and infection with pp-VSV-SARS-CoV-2 spike.

220 Determining dynamic adhesion of CD4(+) T cells to MAdCAM-1 and the in vitro

221 P387 TSP4 was more active in supporting adhesion of cultured human and mouse macrophages in expe

222 Additionally, comparison of adhesion of dipeptides containing Lys and either DOPA (K

223 Herein, we study adhesion of Lys and DOPA-containing peptides to organic

224 d cohesion between osteopontin polymers, and adhesion of osteopontin to hydroxyapatite, enhancing ene

225 for therapy to disrupt peritoneal spread and adhesion of ovarian cancer cells.

226 ational methylation of flagellin facilitates adhesion of Salmonella Typhimurium to hydrophobic host c

227 PG digestion, facilitating the migration and adhesion of Schwann cells on inhibitory aggrecan and ast

228 s but fails to bifurcate because of abnormal adhesion of the periderm.

229 etween nylon and MAHgEO greatly improved the adhesion of these dissimilar materials.

230 drugs targeting the mechanism of osteoclast adhesion onto the bone.

231 th cases, interactions with the substrate by adhesion or friction are widely accepted as a prerequisi

232 homophilic recognition that leads to either adhesion or repulsion between neurites.

233 ough TAVI reduces Mac-1 activation, cellular adhesion, phagocytosis, oxidized low-density lipoprotein

234 olar filament formation but led to divergent adhesion phenotypes and NMIIA contractile activities dep

235 We thus propose that integrin-mediated adhesion pre-dates the emergence of animals.

236 microscopy revealed temporal differences in adhesion, proliferation, bacterial cell physiology and h

237 tegrity of the EVL, likely by mediating cell adhesion properties.

238 decrease in diffusion of up to 85% in dense adhesion protein contacts.

239 lly ascribed to increased levels of the cell adhesion protein E-CADHERIN, which lead to premature dif

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

241 he cytosolic C terminus of the synaptic cell adhesion protein Neuroligin-2 alters the conformation of

242 LRRTM4 is a transsynaptic adhesion protein regulating glutamatergic synapse assemb

243 Neuroligins (Nlgns) are adhesion proteins mediating trans-synaptic contacts in n

244 In addition, the adhesion proteins Roughest and Kirre, which coordinate a

245 Kindlins are focal adhesion proteins that regulate integrin activation and

246 adherin family of Ca(2+)-dependent cell-cell adhesion proteins, which play essential roles in animal

247 oblastoma cells, together with several focal adhesion proteins: vinculin (VCL), talin 1 (TLN1), integ

248 pairment of CAV1- and integrin-mediated cell adhesion, providing insights into the cellular pathogene

249 hRNA screens, we identified the cell-surface adhesion receptor CD44 as a key positive regulator of PD

250 al that integrin alphaIIbbeta3, a prototypic adhesion receptor, can be activated by various mechanica

251 The integrin family of transmembrane adhesion receptors coordinates complex signaling network

252 Integrins are the major cell surface adhesion receptors mediating cell-matrix adhesion in ani

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

254 Analysis of cell-cell adhesion-related proteins in SW480+APC cells revealed an

255 e also independently associated with risk of adhesion-related readmissions.

256 aparoscopic surgery reduces the incidence of adhesion-related readmissions.

257 functions such as cell-matrix and cell-cell adhesion remained unaffected, though these activities di

258 asoconstriction, but its involvement in cell-adhesion remains largely unknown.

259 erall burden of readmissions associated with adhesions remains high.

260 Functional studies included endothelial cell adhesion, shear stress-induced cell alignment, blood pre

261 ces in dynamic equilibrium-salivary flow and adhesion, shedding and colonization-and by interactions

262 which play critical roles in apoptosis, cell adhesion, signal transduction, or metabolite homeostasis

263 tures that consist of two fibronectin-coated adhesion sites connected by a thin guidance cue.

264 mechanism, alpha5beta1 integrin-based focal adhesions slide actively on the underlying matrix toward

265 but does not completely abrogate, neutrophil adhesion, spreading, and crawling under static condition

266 d the MZO(nano) during the initial bacterial adhesion stage.

267 Real-time measurement of cell adhesion, stiffness, and imaging were performed using at

268 tabilized anti-electrostatic linkages, shows adhesion strength comparable to commercial superglue for

269 These data suggest that adhesion strength could potentially serve as a stable ma

270 Hemidesmosomes are specialized cell-matrix adhesion structures that are associated with the keratin

271 domly oriented mimetics did not change focal adhesion tension sensation or enrich for p38-YAP-TEAD in

272 rmation of unusually stable and mature focal adhesions that resisted disassembly induced by the myosi

273 ules, as well as proteins involved with cell adhesion, the cytoskeleton, and apoptosis, were increase

274 ICAM and VCAM expression, elevated leukocyte adhesion to and migration across BMVEC monolayers, and i

275 demonstrate that ITGA2 triggers cancer cell adhesion to collagen, promotes cell migration, anoikis r

276 t mouse, as well as human GPVI, had platelet adhesion to colon and breast cancer cells.

277 employed as water-based primers for PP-metal adhesion to condition PP surfaces and increase adhesive

278 depletion may coordinate VSMC migration and adhesion to different ECM proteins and regulate cellular

279 dies that mediate antigen-specific cell-cell adhesion to effectively overcome the barrier to T6SS act

280 arization, which is important for neutrophil adhesion to endothelia during inflammation.

281 st known for its role in mediating leukocyte adhesion to endothelial cells and guiding leukocytes acr

282 smooth muscle cells and decreased monocytes adhesion to endothelium, as well as reducing TNF-alpha,

283 quired for cell-matrix adhesion confirmed by adhesion to fibronectin-coated plates with cells that ha

284 However, as LT also promotes ETEC adhesion to intestinal epithelial cells, we postulated t

285 cells to lymphatic vessels through selective adhesion to its ligand hyaluronan in the leukocyte surfa

286 bility of AR to induce Bnip3 is dependent on adhesion to laminin and integrin alpha6beta1-dependent n

287 antages including large surface area, robust adhesion to substrates, high areal/specific capacity, fa

288 enes linking integrin signaling and cellular adhesion to the extracellular matrix (ECM) with inhibiti

289 Staphylococcus aureus adhesion to the host's skin and mucosae enables asymptom

290 iotics and antimicrobials, pathogenesis, and adhesion to the mucosal surfaces to colonize the host.

291 Adhesion to vaginal epithelial cells, pH, D/L-lactate pr

292 limited, which explains the paucity of anti-adhesion treatments.

293 onsive mechanism that stabilizes tricellular adhesion under tension during epithelial remodeling.

294 hat RAP1 has a prominent role in cell-matrix adhesion via extracellular matrix molecule fibronectin-i

295 on to the traumatized surface, postoperative adhesion was completely and reliably prevented in three

296 omyosin-driven retraction, and CD44-mediated adhesion, where adhesive and cytoskeletal components are

297 expression of genes implicated in cell-cell adhesion, whereas the expression of negative regulators

298 ion kinase from the signaling layer of focal adhesions, whereas vinculin remained in its normal posit

299 was unsuccessful due to reduced appressorial adhesion, which led to solute leakage.

300 ligned fibril-like structures, which induced adhesion zones between the membranes and the formation o