ライフサイエンスコーパス: adhesion

1 es rapid beta2-integrin-dependent eosinophil adhesion.

2 a front-to-back gradient in membrane-cortex adhesion.

3 ggering mediates chemokine-induced leukocyte adhesion.

4 s a cell wall protein that imparts cell-cell adhesion.

5 to mirror-symmetric pentamers (G-R-B-R-G) by adhesion.

6 several features of THSD7A suggest a role in adhesion.

7 ein-carbohydrate interactions, and cell-cell adhesion.

8 ha treatment also led to enhanced neutrophil adhesion.

9 esmosome and known for its role in cell-cell adhesion.

10 ay, indicated that they may be important for adhesion.

11 in-dependent sickle-red blood cell-leukocyte adhesion.

12 grin by talin is essential for inducing cell adhesion.

13 in macroscale modulus, there is no change in adhesion.

14 ECM that promotes leukocyte infiltration and adhesion.

15 of actin cytoskeleton dynamics and cell-cell adhesion.

16 hymal phenotype and an increase in cell-cell adhesion.

17 negatively regulate integrin activation and adhesion.

18 s cell division orientation to intercellular adhesion.

19 nity homophilic bonds that promote cell-cell adhesion.

20 on of myosin II motors and integrin-mediated adhesions.

21 expressing paxillin-EGFP to visualize focal adhesions.

22 osits via talin1, a major component of focal adhesions.

23 ating the formation and disassembly of focal adhesions.

24 lutch couples actin to previously positioned adhesions.

25 ntitative decreases in TJ and cell-substrate adhesions.

26 geted delivery of integrin vesicles to focal adhesions.

27 the growth inhibitory and neurotoxic or anti-adhesion activities of C3.

28 ated by a complex interplay between cellular adhesions, actomyosin-driven contractility, and the phys

29 prevented increases in VCAM-1 and leukocyte adhesion after treatment with tumour necrosis factor-alp

30 contractile stress, isolated cell speed, and adhesion all play a substantial role in influencing epit

31 In addition, it regulates cell-to-cell adhesion, AMPK signaling, autophagy and apoptosis in dif

32 During cell adhesion, an active multistage process naturally leads t

33 he tight junction (TJ), the apical cell-cell adhesion and a key regulator of the epithelial barrier.

34 y and biological-recognition motifs for cell adhesion and angiogenesis.

35 Therefore, we named this PAI as Locus of Adhesion and Autoaggregation (LAA).

36 ROCK1 was sufficient to rescue keratinocyte adhesion and biochemical differentiation in these mice.

37 INORel combination greatly reduces bacterial adhesion and biofilm formation of two most common pathog

38 ognizes the wound microenvironment, promotes adhesion and biofilm formation, decreases bacterial kill

39 y understood changes in epithelial cell-cell adhesion and cell motility.

40 es coated with tenascin C exhibited enhanced adhesion and colony formation as mediated by integrin al

41 erentially methylated genes function in cell adhesion and communication pathways.

42 contributions of osmotic pressure, cell-cell adhesion and cortical stiffness to mitotic rounding.

43 adhesion and motility mutants have increased adhesion and decreased motility.

44 ion by IL-5-activated eosinophils depends on adhesion and Fcgamma receptor activation, requires eleva

45 We conclude that ICAM-1 augments myoblast adhesion and fusion through its ability to self-associat

46 sP-11 cells increased liver endothelial cell adhesion and liver metastasis.

47 rane trafficking, resulting in impaired cell adhesion and migration in vitro.

48 eins play an active role in coordinating the adhesion and migration machinery in cancer progression.

49 alkine (CX3 CL1), a chemokine that regulates adhesion and migration of leukocytes is expressed by SGN

50 IL-5 enhances eosinophil adhesion and migration on periostin, an extracellular ma

51 bryonic kidney (HEK) 293 cells induced their adhesion and migration to PTN.

52 r leak, possibly through effects on pericyte adhesion and migration, and reveal alphavbeta5 inhibitio

53 ction for this kinase as a modulator of cell adhesion and migration.

54 , which may be harnessed by cells to control adhesion and migration.

55 These regulators of adhesion and motility mutants have increased adhesion an

56 Differences in adhesion and protrusion dynamics were mediated by balanc

57 s of hemodynamics and cytokines on leukocyte adhesion and trans-endothelial migration (TEM) and subse

58 lling pathway, which facilitates endothelial adhesion and transendothelial migration via an ICAM1-fib

59 oducts that regulate immune function or cell adhesion and tumor cell metastasis.

60 howed disruption of filamentous actin, focal adhesions and caveolae-mediated membrane trafficking, re

61 guidance is built on the local alignment of adhesions and individual protrusions.

62 equired by the matrix to break intercellular adhesions and initiate cell invasion.

63 eemed limited, mainly consisting in rolling, adhesion, and aggregate formation.

64 g abilities, antireflection, enhanced color, adhesion, and antimicrobial and specific cell-attachment

65 rocesses underlying palatal shelf elevation, adhesion, and fusion.

66 ns implicated in regulating cell morphology, adhesion, and migration in various cell types.

67 pathways that regulate cell migration, cell adhesion, and proliferation.

68 s, which quantify the extent of solute-water adhesion, and therefore solute hydrophobicity.

69 ulating tumor cell proliferation, migration, adhesion, and transendothelial migration via increased e

70 Focal adhesions are dynamic constructs at the leading edge of

71 he front of the lamellipodium, where nascent adhesions are positioned in rows, and the base of the la

72 surface functionalization, strong interface adhesion as well as boosting the interfacial contact are

73 n the regulation of beta2 integrin-dependent adhesion, as well as in other cellular functions in neut

74 nuclear membrane protein Sun2 promote focal adhesion assembly by activating the small GTPase RhoA.

75 lexes and inhibits RhoA activation and focal adhesion assembly.

76 e to promote actin retrograde flow and focal adhesion assembly.

77 yte adhesion by modulating the expression of adhesion-associated endothelial mRNA targets.

78 cytoskeletal networks failed to support cell adhesion at the BTB.

79 lular stresses that tend to pull cell-matrix adhesions away from the boundary.

80 we introduce, to our knowledge, a new set of adhesion-based biomarkers for characterizing mammalian c

81 dent regulation of DE-Cadherin-mediated cell adhesion between NBs and neighboring cortex glia, and be

82 umber of surface receptors that mediate cell adhesion between RBCs, and between RBCs and white blood

83 ssed cytosolic Ca(2+) oscillations: Hechtian adhesion between the plasma membrane and the cell wall o

84 um = 103 mEq/L), in contrast, decreased sRBC adhesion, but overswelling prolonged sRBC transit times

85 kindlin-2 as a key protein that couples cell adhesion by activating integrins and the induction of me

86 uggesting that these miRs regulate leukocyte adhesion by modulating the expression of adhesion-associ

87 alterations in contraction and/or substrate adhesion can cause confluent epithelial monolayers to ex

88 Oral adhesions can result from a disruption of periderm forma

89 ts with the previously proposed differential adhesion cell sorting.

90 red for Nogo-A-Delta20-induced inhibition of adhesion, cell spreading, and neurite outgrowth, as well

91 ith decreased cell spreading, abnormal focal adhesions, changes in the organization of the actin cyto

92 ogy dependent, as hyphal tubes had increased adhesion compared with yeast cells ( P < 0.05).

93 ction forces to the underlying substrate via adhesion complexes.

94 We propose that defective intercellular adhesion contributes to uncontrolled cSCC growth by prev

95 ension, the lamellipodial actin network, and adhesions coordinate the dynamics of spreading fibroblas

96 thesized that mechanical forces in bacterial adhesion could regulate thioester reactivity to ligand a

97 on neutrophils is the hallmark of leukocyte adhesion deficiency (LAD) syndrome in humans, characteri

98 Human pluripotent stem cells (hPSCs) are adhesion-dependent cells that require cultivation in col

99 It requires a Rho- and E-cadherin adhesion-dependent, substrate-parallel contractile actin

100 itivity to Mg(2+)- and Ca(2+)-mediated focal adhesion disassembly in metastatic cells, rather than ch

101 ably, we uncovered cell state plasticity and adhesion dynamics regulated by Ror2, which influenced Ra

102 entropy difference increases with increasing adhesion energy and decreasing equilibrium binding dista

103 ated to extracellular matrix, immunity, cell adhesion, epigenetic regulation, and airflow obstruction

104 ogy, targeting antifungal efflux and biofilm adhesion factors.

105 130Cas is a Src substrate localized in focal adhesions (FAs) and functions in integrin signaling to p

106 Focal adhesions (FAs) are integrin-based transmembrane assembl

107 Our simulations also predict the adhesion force profile to be distinct for CaCl2 compared

108 may contribute to the reduction of physical adhesion forces between petals and other floral organs d

109 rison between strains demonstrated increased adhesion forces for a clinical isolate compared with the

110 allel to a surface decreased with increasing adhesion-forces acting perpendicular to the surface, (3)

111 l tryptophan ladder or to provide additional adhesion functions.

112 GPR124 (also known as TEM5/ADGRA2) is an adhesion G protein-coupled receptor family member that p

113 major subsets based on the expression of the adhesion G protein-coupled receptor GPR56, and GPR56(+)

114 Cell adhesion genes, JAM-A and FSCN1, were downregulated with

115 tion, small molecule metabolic process, cell adhesion (GO IDs: 0030198, 0044281, 0007155) and pathway

116 Cell surface molecular adhesions govern many important physiological processes

117 519770, P=2.98x10(-)(8)) in an intron of the adhesion GPR98 (G-protein-coupled receptor V1) gene on c

118 a, and increased susceptibility to bacterial adhesion (>3-fold), the epithelium remained resistant to

119 rb spermatogenesis, in particular, spermatid adhesion (i.e., inducing apical ES degeneration) and BTB

120 The presence and regulation of PKD2 at focal adhesions identifies a novel function for this kinase as

121 becomes vulnerable to Pseudomonas aeruginosa adhesion if it lacks the innate defense protein MyD88 (m

122 IQGAP1-Rac1 pathway to strengthen cell-cell adhesion in normal adult crypt stem cells and colon canc

123 and hypoxic conditions, and increasing sRBC adhesion in our microfluidic human microvasculature mode

124 in decreased VCAM-1 expression and leukocyte adhesion in quiescent tumour endothelial cells with inta

125 a dramatic increase in leukocyte rolling and adhesion in veins near the optic nerve (ON) head at 9 ho

126 ydrophobins were upregulated upon early root adhesion, in mycorrhizas or throughout interaction.

127 g and atomistic simulations predict that the adhesion induced entropy difference increases with incre

128 We report that adhesion-induced eosinophil cytolysis takes place throug

129 configuration were used to characterize the adhesion interaction between MoS2 and silicon oxide.

130 ences of mussel proteins, exhibit reversible adhesion interactions significantly exceeding that of an

131 Using adhesion/invasion assays and immunofluorescent and trans

132 dothelial permeability, intravital leukocyte adhesion, involvement of the Akt/WNT/beta-catenin signal

133 Integrin-mediated adhesion is a central feature of cellular adhesion, loco

134 ght into the mechanisms underlying bacterial adhesion is critical to the formulation of membrane biof

135 Leukocyte adhesion is mediated mainly by selectins, cell adhesion

136 Cadherin-mediated homophilic adhesion is necessary for trans-endocytosis, and adhesiv

137 On the nanoscale, however, gecko adhesion is shown to depend on substrate modulus.

138 rlying mechanism of this intriguing gas-like adhesion is the configurational entropy difference betwe

139 Specifically, the disruption of focal adhesion kinase (FAK) and paxillin interactions using th

140 We previously identified focal adhesion kinase (FAK) as an important regulator of cilio

141 entify the adhesion proteins talin and focal adhesion kinase (FAK) as proteolytic targets of calpain

142 a ligand resulted in the activation of focal adhesion kinase (FAK) in a protein kinase C dependent ma

143 Inhibition of focal adhesion kinase (FAK) rescued SERT function in synapses

144 osphorylation of occludin Ser(490) and focal adhesion kinase (FAK) Ser(722) and Tyr(576).

145 port that Src family kinases (SFK) and focal adhesion kinase (FAK) sustain AKT and MAPK pathway signa

146 residue blocks PKD2's interaction with Focal Adhesion Kinase (FAK).

147 ced cytoskeletal changes and activated focal adhesion kinase and ERKs 1/2, and decreased Src kinases

148 We have found that focal adhesion kinase expression is downregulated under a high

149 ght chain kinase or phosphorylation of focal adhesion kinase was ineffective.

150 usly reported in separate studies that focal adhesion kinase-1 (FAK) and the chemokine receptor CXCR4

151 bsequently measured single-integrin-molecule adhesion kinetics using an optical trap, and diffusion u

152 nt contractility, a characteristic viscosity-adhesion length, and a rate of actin protrusion.

153 g SNPs in or near genes involved in cellular adhesion, leukocyte migration and atherosclerosis (PECAM

154 n stability and persistence are functions of adhesion lifetime, which depends on fiber orientation.

155 ed adhesion is a central feature of cellular adhesion, locomotion, and endothelial cell mechanobiolog

156 The LP cells demonstrated an adhesion macromolecule expression pattern distinct from

157 molecular level, the sites of abnormal oral adhesions maintained periderm-like cells that express ke

158 ), a protein that plays a vital role in cell adhesion, making it a biologically plausible candidate g

159 23 promoted stress fiber formation and focal adhesion maturation in a dynamin-dependent manner.

160 regulated responses to homing signals and/or adhesion mechanisms that influenced their ability to col

161 main boundaries sharpen through differential adhesion-mediated cell sorting.

162 ween intracellular annexin A2 and tumor cell adhesion, migration and in vivo grafting.

163 mutation had moderate abnormalities in cell adhesion, migration, proliferation and growth factor-dep

164 Down syndrome cell adhesion molecule (Dscam) is expressed by mouse RGCs sho

165 The neural cell adhesion molecule (NCAM) is the major carrier of polysia

166 is a glycan modification of the neural cell adhesion molecule (NCAM) produced by the polysialyltrans

167 We find that intercellular adhesion molecule 1 (ICAM-1) and ICAM-2 on B cells are e

168 y alterations, and crawling on intercellular adhesion molecule 1 (ICAM-1)-expressing cells.

169 ion of an inflammatory marker, vascular cell adhesion molecule 1 (VCAM-1), in atherosclerotic plaques

170 r of metalloproteinases 1; and vascular cell adhesion molecule 1 [VCAM-1]) were measured by using enz

171 (CD34, endomucin, platelet endothelial cell adhesion molecule 1, and plasmalemmal vesicle-associated

172 h soluble and immobilized intercellular cell adhesion molecule 1.

173 1 and beta2; thrombospondin 2; intercellular adhesion molecule 1; interleukin 6 [IL-6]; stromal cell-

174 thelial MPs, epithelial MPs (epithelial cell adhesion molecule [EpCAM](+)MPs, E-cadherin(+)MPs), plat

175 of claudin 1 (CLDN1), CLDN4, and junctional adhesion molecule A (JAM-A) subunits is induced at the G

176 CD169 is a Siglec that may function as an adhesion molecule and a facilitator of the recognition a

177 dothelial selectin and soluble intercellular adhesion molecule concentrations decreased (P < 0.001).

178 Simvastatin modified surface adhesion molecule expression and activity, facilitating

179 iR-100 as a potent suppressor of endothelial adhesion molecule expression, resulting in attenuated le

180 as Vegfa/VEGFR1+2 upregulation or increased adhesion molecule expression.

181 igand-1 (PSGL-1) has long been studied as an adhesion molecule involved in immune cell trafficking an

182 ly relevant to skin homeostasis: neural cell adhesion molecule L1 and dipeptidyl peptidase 4.

183 ng of multiple receptors, including the cell adhesion molecule L1/NgCAM, the neurotransmitter recepto

184 g CIL requires the participation of the cell adhesion molecule N-cadherin, which starts to be express

185 d its major protein carrier, the neural cell adhesion molecule NCAM, play important roles in many ner

186 concomitant with reduction of intercellular adhesion molecule-1 (ICAM-1) and diminishing the enzymat

187 ese cells through reduction of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion

188 hesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1).

189 he metastasis-related proteins intercellular adhesion molecule-1 and urokinase-type plasminogen activ

190 sis factor receptor-1, soluble vascular cell adhesion molecule-1, granulocyte colony-stimulating fact

191 Our results identify cell-adhesion molecule-mediated inhibition as a regulator of

192 D122(-)PD1(+)CD44(+)CD62L(-)) and expressing adhesion molecules (VLA-4(+)LFA-1(+)) complementary to a

193 hesion is mediated mainly by selectins, cell adhesion molecules and chemokines induced by pro-inflamm

194 nd plays key roles in regulating NK ligands, adhesion molecules and cytokine receptors.

195 Locally, adhesion molecules are distributed at the tips of membra

196 The up-regulation of cell surface adhesion molecules by BMP9/10 in the presence of TNFalph

197 rface expression of beta1 and beta2 integrin adhesion molecules by using flow cytometry.

198 attenuated the expression of chemokines and adhesion molecules in endothelial cells and reduced NF-k

199 ic inflammatory markers and soluble vascular adhesion molecules were measured in plasma samples of da

200 urotransmitter receptors, cell signaling and adhesion molecules, and ciliary intraflagellar transport

201 microvascular endothelial cells to stimulate adhesion molecules, CCL2, ICAM1, VCAM1 and cytokines, IL

202 vented the induced expression of the crystal adhesion molecules, CD44 and annexin II, in tubular epit

203 proximately 40 gene families, including cell-adhesion molecules, transmitter-modulator receptors, ion

204 e up-regulation of endothelial selectins and adhesion molecules, ultimately resulting in increased mo

205 target genes encode diverse epithelial cell adhesion molecules, while mesenchymal genes involved in

206 ed Nav and Kv7 channels associated with cell adhesion molecules.

207 eractions between pre- and postsynaptic cell-adhesion molecules.

208 -regulation of proinflammatory cytokines and adhesion molecules.

209 volved in chromatin organization, signaling, adhesion, motility, development and metabolism.

210 lving regulation of beta2-integrin-dependent adhesion, NADPH oxidase, and a subset of protein kinases

211 adherent, which contrasts with the increased adhesion observed in the tube region.

212 tantially larger than the interaction of the adhesion of a pleckstrin homology domain with phosphatid

213 The tube surface is resistant to adhesion of activated platelets unlike planar control ti

214 M force-spectroscopy results showed that the adhesion of C. albicans to PMMA is morphology dependent,

215 Adhesion of cancer cells to endothelial cells is a key s

216 tern of endothelial cells and thereby impact adhesion of circulating cells.

217 Self-assembly of PNPs on PGE surface and adhesion of DLD-1 cancer cells on this surface was also

218 aces may underlie the difference in cellular adhesion of hNSCs reported here.

219 Rac3 GTPase is critical for integrating the adhesion of invadopodia to the extracellular matrix (ECM

220 accommodate the alphaLbeta2-mediated rolling adhesion of leukocytes.

221 s structure of the CNF paper rendered strong adhesion of the AZO layer and exhibited excellent mechan

222 Cytosine nucleobases are shown to alter the adhesion of the DNA to SWCNTs through direct protonation

223 how a clear dependence of melanoma cell-cell adhesion on pHe and NHE1 as a modulator.

224 nanoscale substrate modulus on whole animal adhesion on two different substrates (cellulose acetate

225 ed moisture barrier, wettability and surface adhesion onto fruit surfaces were developed for controll

226 low: PD1n-3 DPA and RvD5n-3 DPA reduced cell adhesion onto TNF-alpha-activated human endothelial mono

227 uction of pattern recognition receptor, cell adhesion, or chemotaxis genes in macrophages.

228 een the LRP4-MuSK pathway and integrin-focal adhesion pathway.

229 lpha5beta1-specific blockade inhibited focal adhesion phosphorylation and IL-13-enhanced contraction,

230 than changes in integrin expression or focal adhesion phosphorylation.

231 of extracellular matrix remodeling and focal adhesion processes in tumors with high TF, supporting th

232 ndidate P. falciparum thrombospondin-related adhesion protein (PfTRAP) expressed in the ChAd63-MVA sy

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

234 g to support the Sertoli cell morphology and adhesion protein complexes (e.g., occludin-ZO-1, CAR-ZO-

235 -2, which is primarily recognized as a focal adhesion protein in EC, was not anticipated to have a ro

236 pper-containing amine oxidase human vascular adhesion protein-1 also exclusively displayed high-manno

237 The neuroligin family cell adhesion proteins NL1, NL2, and NL3, which are expressed

238 of many biological molecules, including the adhesion proteins of several marine organisms.

239 Here, we identify the adhesion proteins talin and focal adhesion kinase (FAK)

240 key role in regulating the activity of focal adhesion proteins.

241 The leukocyte adhesion receptor L-selectin forms bonds with P-selectin

242 ress high levels of beta1 and beta2 integrin adhesion receptors.

243 In both normal and adhesion-reduced ectoderm, cortical tension of the free

244 ed cytoskeletal dynamics contributes to cell adhesion regulation during intestinal wound repair and t

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

246 dominal wall procedure), and complexity (eg, adhesions; relative value units).

247 The assembly of focal adhesions requires the recruitment and activation of vin

248 0.05) upon rhizosphere colonization and root adhesion respectively.

249 luorescent analyses of the periderm and oral adhesions revealed the presence of Arhgap29 in periderm

250 ain increases the localization of endogenous adhesion signaling to growth cone filopodia.

251 targeting mechanism for properly localizing adhesion sites during cell motility.

252 mechano-responsive properties of N-cadherin adhesion sites in isolated VSMCs.

253 defective farnesylation mislocalizes nascent adhesion sites, suggesting that LKB1 farnesylation serve

254 Neuronal synapses are adhesions specialized for communication and they come in

255 interlocking, thereby achieving significant adhesion strength ( 1.6Ncm(-2)) with rat skin.

256 elates of parameters in the model: substrate adhesion strength, actin polymerization rate, myosin con

257 The adhesion system formed by neurexins (Nrxns) and neurolig

258 Understanding the adhesion system's performance on various surfaces can gi

259 es (HDs) are epithelial-specific cell-matrix adhesions that stably anchor the intracellular keratin n

260 plexes, linked by Celsr1-mediated homophilic adhesion, that coordinate polarity non-autonomously betw

261 in, while integrins function at the level of adhesion, the importance of lectins remains unknown.

262 we demonstrate that KCa1.1 regulates RA-FLS adhesion through controlling the plasma membrane express

263 tumor cell rolling on selectins facilitates adhesion to a distinct substrate-bound protein with diff

264 beta1, while hemoglobin AS did not modify IE adhesion to any receptors.

265 hat FlnA negatively regulates beta2 integrin adhesion to complement component iC3b and ICAM-1 in shea

266 avasation and metastasis by facilitating the adhesion to endothelial cells and transendothelial extra

267 RNA in endothelial cells enhanced neutrophil adhesion to endothelial cells but inhibited neutrophil t

268 nvasion increased due to increased bacterial adhesion to epithelial monolayers with compromised cell-

269 tegrin alphavbeta3, is activated through HSC adhesion to extracellular matrix and niche cells.

270 RASF adhesion to GF(+) matrix resulted in the strongest IL-6

271 at this interaction contributes to bacterial adhesion to host cells, invasion of host tissues, and ev

272 Bacterial adhesion to host receptors is an early and essential ste

273 on Willebrand factor (VWF) mediates platelet adhesion to injured vessels by sequestering platelets fr

274 croscopy showed that SdrF mediates bacterial adhesion to keratin 10 through strong and weak bonds inv

275 We report that ICAM-1 augments myoblast adhesion to myoblasts and myotubes through homophilic tr

276 g, enhanced biofilm formation, and increased adhesion to nasopharyngeal cells.

277 Leukocyte adhesion to P-selectin on activated platelets and endoth

278 low chamber, targeted MB exhibited increased adhesion to platelets as compared to MBControl.

279 ecular mechanisms that limit ICAM-1-mediated adhesion to prevent excessive leukocyte transmigration r

280 hat SCARF-1 contributes to lymphocyte subset adhesion to primary human HSEC and could play an importa

281 Bacterial adhesion to surfaces occurs ubiquitously and is initiall

282 ted neutrophil infiltration, tumor cell (TC) adhesion to the endothelium, intravasation, lung coloniz

283 LN-511-E8 resulted in firm integrin-mediated adhesion to the scaffold and well-stratified epithelial

284 the coordination of cell length changes with adhesion to the surface.

285 Finally, we present evidence that adhesion to the UF membrane surface is mediated by cell-

286 te for the molecular parameters for schizont adhesion to the vascular endothelium and to predict bond

287 ntly attenuated for colonization in mice and adhesion to uroepithelial cells.

288 ms to 130% for multilayer films, causing the adhesion toughness G c to decrease from 0.424 J m(-2) to

289 psilon1 was necessary for SDF-1alpha-induced adhesion using shear stress, cell morphology alterations

290 bonds involving the A and B regions; strong adhesion was primarily mediated by the A region.

291 sylation is an important determinant of cell adhesion, we hypothesized that radiation could alter the

292 genes related to neurotransmission and cell adhesion were altered in the brain of Crmp4-KO mice, mos

293 F2A regulated genes involved in fibrosis and adhesion, whereas in the ventricles, it controlled infla

294 ding proliferation, migration, and cell-cell adhesion, which are all requisite for angiogenesis.

295 -cell receptor (BCR) signaling and migration/adhesion, which could contribute to the proliferation, s

296 tween embryonic implantation and cancer cell adhesion, which suggests that abortifacients may be good

297 rgeons should approach laparoscopic lysis of adhesions with a higher level of awareness and use strat

298 ient assigned to placebo reported intestinal adhesions with obstruction as a severe and serious adver

299 disrupts the integrity of TJ and cell-matrix adhesions, with indicators of cellular stress with liver

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