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1 recognize sialic acid as receptors for host cell attachment.
2 and normalized vessels with increased mural cell attachment.
3 esults in reduced virulence and impeded host cell attachment.
4 shows that these factors contribute to host cell attachment.
5 t embryos exhibit a failure in muscle-tendon cell attachment.
6 rin alpha6beta4, which often mediates stable cell attachment.
7 t-1 can be counteracted by integrin-mediated cell attachment.
8 nt and biofilm formation, thereby inhibiting cell attachment.
9 ar F-actin bundles, particularly at areas of cell attachment.
10 ved in important cellular processes, such as cell attachment.
11 cytotoxicity while providing a substrate for cell attachment.
12 otein product, TGFBIp, mediates an effect on cell attachment.
13 ed that deleting the five TA systems reduced cell attachment.
14 s uniquely counteracted by integrin-mediated cell attachment.
15 tantiating their possible role in initiating cell attachment.
16 the Akt signaling pathway and enhanced PC-3 cell attachment.
17 s the hinged short tail fibers to facilitate cell attachment.
18 4002 (an inhibitor of Akt signaling) reduced cell attachment.
19 integrins, localizing urokinase to sites of cell attachment.
20 ainst alphaVbeta3 did not have any effect on cell attachment.
21 ation is the adhesion of protein followed by cell attachment.
22 ), and block the normal function of GPR56 in cell attachment.
23 virus infectivity, presumably blocking host-cell attachment.
24 moted increased cell survival after 1 day of cell attachment.
25 a1-mediated adhesion, whereas Pyk2 opposes T-cell attachment.
26 ated increased cell survival after 3 days of cell attachment.
27 tirely accounted for by the decrease in host cell attachment.
28 of effects on translocation from effects on cell attachment.
29 aracterized cs defect directly affected host cell attachment.
30 e, probably inhibiting infection by blocking cell attachment.
31 owed increased biofilm formation and cell-to-cell attachment.
32 nspecific protein, fibroblast, and bacterial cell attachment.
33 ults in a light-independent increase in cell-cell attachment, a response that requires both the conse
35 t, whereas mutant rec-M2 and rec-M3 retained cell attachment activity but did not promote cell spread
36 aminin alpha5 globular domain (G-domain) for cell attachment activity with B16-F10 cells using peptid
37 principle be the result of weak, incomplete cell attachment, adhesion is usually too strong for this
39 ecombinant Scl-1 protein suggested a role in cell attachment and binding and inhibition of serum prot
41 acts with two similar proteins that regulate cell attachment and cell migration called paxillin (PXN)
42 bility of three titanium surfaces to promote cell attachment and cell motility of cells relevant to p
47 bition of TG2 by siRNA-inhibited Fn-mediated cell attachment and cell survival functions in drug-resi
48 d FAK tyrosine phosphorylation increase upon cell attachment and decrease upon detachment from extrac
50 el such as cell migration or the dynamics of cell attachment and detachment are also addressable by o
54 the utilization of conjugative plasmids for cell attachment and entry comprises independent evolutio
59 bacterial surface polysaccharides, enhancing cell attachment and environmental stability, potentially
63 ) surface glycoprotein (GP1,2) mediates host cell attachment and fusion and is the primary target for
64 d surface were demonstrated: (1) a guide for cell attachment and growth and (2) a substrate for immun
65 th cells, suggesting a detrimental impact on cell attachment and growth when conditioning by this age
66 ipeptide, RGD, and experiments comparing the cell attachment and haptotactic migration-enhancing prop
72 F. nucleatum 12230 US1 was defective in host cell attachment and invasion in vitro, but it also exhib
73 d in increased anchorage-independent growth, cell attachment and invasion through Matrigel in vitro,
77 es anchorage-independence by driving cell-to-cell attachment and matrix-independent integrin beta4/SH
78 protein (GP), responsible for mediating host-cell attachment and membrane fusion, contains a heavily
85 as a scaffolding protein with activities in cell attachment and mitotic control, suggesting SRC and
88 ysis showed that GelMA supported hDPSC/HUVEC cell attachment and proliferation and also provided atta
89 ior, WN-1 displays PMA-like behavior in U937 cell attachment and proliferation assays, as well as in
90 riments with PDL cells demonstrated improved cell attachment and proliferation in all samples coated
92 sponses to cell adhesion--enhanced mammalian cell attachment and proliferation, and enhanced resistan
93 rbed to the culture surface, promoted H1 hES cell attachment and proliferation, as well as maintained
97 en has the potential to improve both initial cell attachment and retention of endothelial cells on va
98 ons, in vitro flow assays demonstrate that T cell attachment and rolling are markedly attenuated in e
101 adaptor function at least partly rescues the cell attachment and skeletal phenotypes, the contributio
102 cted, because Spry2 dramatically facilitates cell attachment and spreading by enhancing focal adhesio
103 l surface and a corresponding enhancement of cell attachment and spreading on fibronectin-coated subs
104 e ability of syndecan-4 molecules to support cell attachment and spreading without the direct extrace
105 uption of the actin cytoskeleton and prevent cell attachment and spreading, whereas mAb addition to c
111 ts how they mediate in a unique fashion both cell attachment and the initiation of membrane fusion du
112 s were activated with fibronectin to mediate cell attachment and the silicon oxide background was pas
113 tracellular matrix environment that promotes cell attachment and tissue-specific differentiation lead
114 t to those of all other reported AAVs, AAV12 cell attachment and transduction do not require cell sur
117 show that epithelial-derived FN potentiates cell attachment and wound healing through epithelial-mat
120 important virulence factors involved in host cell attachment and/or biofilm formation, key steps in e
122 acidic phosphoprotein with collagen-binding, cell attachment, and hydroxyapatite-nucleating propertie
124 ar activities, including transcription, cell-cell attachment, and regulation of the cytoskeleton.
125 tructural surface features can guide cardiac cell attachment, and the subsequent syncytial behavior c
126 Focal adhesions (FAs) play a key role in cell attachment, and their timely disassembly is require
127 ectly or indirectly required for maintaining cell attachment, and this may represent a common but not
129 PGER sequence prevented integrin binding and cell attachment as predicted from molecular dynamics stu
130 els of VE-cadherin expression, and increased cell attachment, as evidenced by Evans blue dye injectio
131 LDL) was responsible for the blockade of HCV cell attachment, as VLDL-depleted mouse serum lost HCV-i
132 gues evaluated in the U937 proliferation and cell attachment assays displayed phorbol ester-like and/
133 I was determined with the use of fluid-phase cell attachment assays in HSFs, human foreskin fibroblas
134 ior activity in opsonophagocytic killing and cell attachment assays, and confer significant protectio
135 oproteins, thereby facilitating Sertoli-germ cell attachment at a particular stage of spermatogenesis
138 lence factors used by P. aeruginosa for host cell attachment, biofilm formation, and twitching motili
139 on of Bit1 is inhibited by integrin-mediated cell attachment but not by many other antiapoptotic trea
140 es but not DeltaIDR2 virus displayed reduced cell attachment, but altering sigma1 length or flexibili
141 rus-adenovirus receptor (CAR) for virus-host cell attachment, but subgroup B and subgroup D (adenovir
142 ellular matrix components because preventing cell attachment by forced suspension culture markedly re
143 harides, which enhances virion stability and cell attachment by increasing binding to the viral recep
146 three stages of integrin-mediated adhesion: cell attachment, cell spreading, and formation of focal
147 WCNT-induced cellular changes in relation to cell attachment, cell-cell interactions and cell viabili
148 ng molecules through which integrin-mediated cell attachment controls Bit1 activity and anoikis.
149 lls that exhibit growth factor-independence, cell attachment defects, and a more invasive fibroblasti
150 units), which is solely responsible for host cell attachment, endosomal entry and membrane fusion.
152 golipids found in cancer cells may influence cell attachment events by direct effects on integrin clu
153 ated for many years, is indeed a major serum cell attachment factor particularly for tumor cells.
155 ls, and are recognized as susceptibility and cell attachment factors for gastric pathogens like Helic
157 n of a cohesive passive layer, after initial cell attachment, followed by the formation of a metal co
158 several critical virus functions, including cell attachment, host range susceptibility, and virulenc
159 Alpha2(VIII) collagen supported endothelial cell attachment in a dose-dependent manner, with an 18-f
161 Therefore, identifying factors regulating cell attachment in the abdominal cavity is critical to t
162 nce of blue light dramatically enhances cell-cell attachment in the lovK-lovR overexpression backgrou
163 eptor binding protein that serves to mediate cell attachment in vitro when using coxsackie-adenovirus
164 tle out-of-plane microtopographic cues alter cell attachment, increase biomechanical stresses, and in
165 Silencing of DLC2 in human ECs has reduced cell attachment, increased migration, and tube formation
166 ncentration-dependent inhibition of Jurkat T-cell attachment, inhibition of lymphocyte activation, an
167 ens, filamentous growth is critical for host-cell attachment, invasion into tissues, and virulence.
168 ed disease in our model, perhaps by reducing cell attachment/invasion and dampening inflammation by m
171 intricate protein complexes that facilitate cell attachment, migration, and cellular communication.
172 0 reference cells were analyzed by measuring cell attachment, migration, and chemotaxis in the presen
174 cytoskeleton and mediate signals modulating cell attachment, migration, proliferation, differentiati
175 e in biologically diverse functions, such as cell attachment, mobility, proliferation, and extracellu
178 that play important roles in motility, host cell attachment, moving junction formation, and invasion
182 demonstrated that apolipoprotein E mediates cell attachment of hepatitis C virus (HCV) through inter
183 whereas rTGFBIp did not significantly affect cell attachment of HFFs (P = 0.50) or HCFs (P = 0.24) to
184 When produced, NanI can contribute to host cell attachment of human intestinal disease strains, sin
187 As with many other viruses, the initial cell attachment of rotaviruses, which are the major caus
188 he Mam7 protein, which is implicated in host cell attachment of V. cholerae, associated normally with
189 riation of glycan recognition during initial cell attachment of viruses is a critical determinant of
191 aled significantly higher osteoblast and PDL cell attachment on EMD-coated surfaces when compared wit
192 Importantly, microRNA-7 decreased Caco2-BBE cell attachment on laminin-1, and CD98 overexpression re
195 t that the M1 and M5 sites are necessary for cell attachment on LG4 through syndecans and that the EF
202 small oscillatory motions within the primary cell attachment plane, rather than perpendicular to it,
203 n actin-binding protein that participates in cell attachment, plays important additional roles in sig
205 ve/Dead cytotoxic assay and displayed higher cell attachment, proliferation and mineralization than t
206 de effects on in vitro measures of fibrosis: cell attachment, proliferation and viability, and ECM de
207 gest that 1) EMD enhances osteoblast and PDL cell attachment, proliferation, and differentiation on N
208 g inhibitory effects of JSM6427 on human RPE cell attachment, proliferation, and migration is probabl
210 helium (RPE) and its ability to modulate RPE cell attachment, proliferation, migration, and F-actin c
211 stratum compliance and/or Lat-B treatment on cell attachment, proliferation, surface area, aspect rat
213 we present new evidence indicating that the cell attachment properties of sigma1 are influenced by t
216 on, but rather with depressed expression the cell attachment protein FAK, accompanied by increased se
217 that requires coordinated activities of host cell attachment, protein secretion, and motility by the
218 ons of herpes simplex virus with its initial cell attachment receptor induce a rapid and highly effic
219 that expression of the Epstein-Barr virus B-cell attachment receptor, CD21, in B cells that lack thi
221 adaptable drop-plating method for selective cell attachment, removal of myelin debris, and expansion
225 In this work, dual electrochemical pH and cell-attachment sensor arrays were developed for the rea
226 Further supporting a role for NanI in host cell attachment, sialidase inhibitors reduced F4969 adhe
229 signals are recorded and analyzed (i) during cell attachment, spreading and differentiation of initia
232 These modified Scl2 proteins also acted as cell attachment substrates for fibroblast, endothelial,
235 nitor the formation of two distinct forms of cell attachment, temporary and permanent, during early b
236 MMP20 would result in tight ameloblast cell-cell attachments that may cause maturation-stage enamel
237 o-glycolic) acid (PLGA) particles to enhance cell attachment, the attachment procedure to avoid clump
238 e domains of TEM8 were sufficient to provide cell attachment, the intracellular domain was critical f
239 cal adhesion-associated protein that reports cell attachment through a RhoA-dependent mechanosensory
241 nt on high-titer viremia; however, efficient cell attachment through HS binding can increase virulenc
243 hanotransductive response for integrin-based cell attachments through our elastomeric membrane-based
244 HPV) infection involves multiple steps, from cell attachment, through endocytic trafficking towards t
245 ve an important role in bacterial epithelial cell attachment, through ILK-bacterial OspE binding.
247 gene, lovR, results in severe attenuation of cell attachment to a glass surface under laminar flow, w
248 ed by p190RhoGAP following integrin-mediated cell attachment to allow sampling of new adhesive enviro
249 tin stress fibers, is inhibited upon initial cell attachment to allow sampling of the new adhesive en
252 c-5 expression increases following mesangial cell attachment to collagen I, associated with increased
254 The effect of rTGFBIp (50 microg/mL) on cell attachment to collagen type I was determined with t
255 in mediating events triggered by epithelial cell attachment to ECM; EGFR is necessary for activation
256 cells at the vascular endothelium, melanoma cell attachment to endothelial cells was significantly d
259 the anoikis function of Bit1, we found that cell attachment to fibronectin inhibits PKD activity.
260 a1 antagonist, significantly inhibited hfRPE cell attachment to fibronectin, but not laminin, or coll
263 ell as preventing inappropriate inflammatory cell attachment to LECs, D6 is specifically involved in
267 function of polar development is to maximize cell attachment to surfaces and to improve nutrient upta
268 Skp-2 expression was absolutely dependent on cell attachment to the ECM and was inhibited by laminin
270 se results suggest the operation of specific cell attachment to the electropolymerized films via the
271 ently controls integrin-mediated endothelial cell attachment to the extracellular matrix and migratio
272 perform the critical function of signalling cell attachment to the extracellular matrix or to other
273 Focal adhesions are specialized sites of cell attachment to the extracellular matrix where integr
277 cellent outgrowth of CNS neurons in vitro by cell attachment to the high density of arginine-glycine-
279 as observed on the cell viability during the cell attachment to the surface of immune-reactive biochi
280 d trypsinization revealed firm protein-based cell attachment to the underlying extracellular matrix f
281 difference in the degree of lens epithelial cell attachment to the various types of intraocular lens
282 gy is induced upon loss of integrin-mediated cell attachments to the surrounding extracellular matrix
283 and strains of CPV differed in the levels of cell attachment, uptake, and infection in canine and fel
285 from purified virions had no effect on virus-cell attachment, virus-cell fusion, particle infectivity
287 Fractionation of human serum revealed that cell attachment was confined to the fractions that had f
290 sed nuclear accumulation of Twist1 following cell attachment was suppressed by treatment with an inhi
293 ponse regulators, and genes for invasion and cell attachment were prominent among the differentially-
294 LADRAD decreased its ability to promote oTr cell attachment, whereas mutation of the CRD had little
295 n remarkable reductions of HCV infection and cell attachment, whereas SDC-3 and SDC-4 knockouts did n
296 to use virally encoded envelope proteins for cell attachment, which is the very first step of virus i
298 s inhibited by blocking PVRL4-driven cell-to-cell attachment with monoclonal antibodies, demonstratin
299 balance, we next compared the time course of cell attachment with the washed films and demonstrated t
300 es demonstrated that mouse serum blocked HCV cell attachment without significant effect on HCV replic
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