ライフサイエンスコーパス: adhesion receptor

1 res of an integrin-like extracellular matrix adhesion receptor.

2 of focal adhesion kinase and integrin alpha5 adhesion receptor.

3 r tyrosine kinase that acts as a collagen IV adhesion receptor.

4 in persons with high levels of this soluble adhesion receptor.

5 , CX3CR1 has been proposed to function as an adhesion receptor.

6 tion and inhibiting its function as a matrix adhesion receptor.

7 RAIL) on their surface along with E-selectin adhesion receptor.

8 remodeling of F-actin and redistribution of adhesion receptors.

9 arity is regulated in part by signaling from adhesion receptors.

10 tly by inadequate expression of cell surface adhesion receptors.

11 in driving the lateral, cis-, clustering of adhesion receptors.

12 motif that can bind to cell-surface integrin adhesion receptors.

13 ng in addition to their well-defined role as adhesion receptors.

14 herin would affect expression of cell matrix adhesion receptors.

15 te for the cytoplasmic tails of the integrin adhesion receptors.

16 1 and occupies the binding site for integrin adhesion receptors.

17 chronous sideways movement of beta1 integrin adhesion receptors.

18 sequence similarity to known matrix protein adhesion receptors.

19 substrates capable of engaging specific cell-adhesion receptors.

20 s the modulation of the affinity of integrin adhesion receptors.

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

22 rease in the functional activity of integrin adhesion receptors.

23 dentified for a member within this family of adhesion receptors.

24 al cooperativity between integrins and other adhesion receptors.

25 and down-regulating cytokine, chemokine, and adhesion receptors.

26 nderstanding the regulation of integrin cell adhesion receptors.

27 ell migration initiated by growth factor and adhesion receptors.

28 ation is initiated by the selectin family of adhesion receptors.

29 tral property of the integrin family of cell adhesion receptors.

30 performed in animal models deficient in both adhesion receptors.

31 ation of the beta(1) integrin family of cell adhesion receptors.

32 d to various chemotactic signals and express adhesion receptors.

33 othelial surface by altering the dynamics of adhesion receptors.

34 olding may be applicable for many other cell adhesion receptors.

35 rotein ELMO, downstream of cell-surface cell-adhesion receptors.

36 the binding specificities and energetics of adhesion receptors.

37 pholipase D (lysoPLD) that binds to integrin adhesion receptors.

38 ment are dependent on the integrin family of adhesion receptors.

39 egulated changes in the affinity of integrin adhesion receptors ("activation") play an important role

40 1-MMP proteolysis of the T cell surface CD44 adhesion receptor affects the homing of T cells into the

41 as to the mechanism of lateral clustering of adhesion receptors after cell-cell contact and, more gen

42 down-regulated the expression of major cell adhesion receptors (alphav and beta3 integrins), matrix

43 in receptor, alpha(5)beta(1)-integrin, as an adhesion receptor and in angiogenesis is well establishe

44 Although biochemical factors such as adhesion receptor and ligand concentration and binding,

45 activated by engagement of several leukocyte adhesion receptors and contribute to both early morpholo

46 migration, rather little is known about the adhesion receptors and extracellular matrix molecules in

47 t is likely that analysis of the spectrum of adhesion receptors and extracellular matrix proteins can

48 Integrin cell adhesion receptors and fibronectin, one of their extrace

49 mposed of clusters of transmembrane integrin adhesion receptors and intracellular proteins that link

50 CAR is a member of the JAM family of adhesion receptors and is located to both tight and adhe

51 Cell invasion requires cooperation between adhesion receptors and matrix metalloproteinases (MMPs).

52 Surface adhesion properties regulated by adhesion receptors and membrane tethers are critical in

53 ar signaling pathways, which are mediated by adhesion receptors and other transducers of extracellula

54 are regulated by a controlled interaction of adhesion receptors and proteases, and late metastasis is

55 on and invasion and endocytic trafficking of adhesion receptors and signaling proteins plays a major

56 d to cell surfaces through interactions with adhesion receptors and sulfated glycolipids (Figure 1, b

57 ate the steady-state levels of signaling and adhesion receptors and that loss of these proteins can c

58 tes mitochondrial injury-induced shedding of adhesion receptors and that TACE activity correlates wit

59 ha-actinin with actin filaments and integrin adhesion receptors and that the dynamics of alpha-actini

60 o GTPases that control the interplay between adhesion receptors and the cytoskeleton.

61 ubunit member of the integrin family of cell adhesion receptors and was found to activate complex of

62 an essential role in activation of integrin adhesion receptors, and expression of at least 1 Kindlin

63 w the actin cytoskeleton and its regulators, adhesion receptors, and scaffolding proteins mediate syn

64 These results document a novel mechanism of adhesion receptor- and pulmonary chemokine-dependent reg

65 ity of a mechanomodulatory drug and integrin adhesion receptor antibodies.

66 Integrin adhesion receptors appear to be regulated by molecules t

67 nals linking the actin cytoskeleton and cell adhesion receptors are essential for morphogenesis durin

68 f membrane bound (2D) and freely moving (3D) adhesion receptors are expressed and compared using elem

69 The integrin family of cell adhesion receptors are important for a diverse set of bi

70 Thus, our results establish the adhesion receptor as a bona fide mechanosensor that dire

71 Moreover, a2NTD treatment activates surface adhesion receptors, as well as FAK and Src kinases that

72 Integrins are heterodimeric adhesion receptors associated with bidirectional signali

73 ication between an inflammatory mediator and adhesion receptors at a molecular level, through selecti

74 here that in rat and mouse, hippocampus cell adhesion receptors belonging to the beta1-integrin famil

75 esent study provides the first evidence that adhesion receptors belonging to the integrin family modu

76 Thus, VWF likely uses other adhesion receptors besides GPIbalpha in thrombus growth

77 o examine the role of the signaling and cell-adhesion receptor beta 4 integrin during ErbB2-mediated

78 combination of chemokine receptor (CCR2) and adhesion receptor (beta2 integrin) engagement leads to a

79 PTP)-PEST and the extracellular matrix (ECM) adhesion receptor beta8 integrin that plays essential ro

80 We use membrane-anchored DNA as model adhesion receptors between lipid vesicles.

81 In their biological context, adhesion receptors bind to an immobile ligand and the bi

82 try modulated FN structure to alter integrin adhesion receptor binding.

83 extracellular matrix or involved in cellular adhesion, receptor binding and hormone activity.

84 s not function as a neutrophil phagocytic or adhesion receptor, but may instead serve as a sugar-bear

85 Neutrophils lacking the chemotactic or adhesion receptor C5a receptor (C5aR) or CD11a/lymphocyt

86 We previously found that the LW RBC adhesion receptor can be activated by epinephrine to med

87 Integrin adhesion receptors can signal in two directions: first,

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

89 bind with high nanomolar affinities to mouse adhesion receptor CD155.

90 such that PS was compared to the erythrocyte adhesion receptor CD36.

91 of increasingly narrow specificity, and PLT adhesion receptors (CD41, CD42b, and CD62P).

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

93 cortical patches, decreased abundance of the adhesion receptor CD44 at membrane protrusions, and atte

94 ve actin assembly and down-regulation of the adhesion receptor CD44 in MM HSPCs functionally reflecte

95 rs the splicing pattern of mRNA encoding the adhesion receptor CD44, promoting exon inclusion, and de

96 N-cadherin is a homotypic cell-cell adhesion receptor commonly overexpressed in tumor cells

97 Dystroglycan is part of an adhesion receptor complex linking the extracellular matr

98 main; and (iii) N-glycosylated transmembrane adhesion receptors complexed with tetraspanin and gangli

99 We describe structures of select adhesion receptor complexes and their assembly into larg

100 , which represent a major group of cell-cell adhesion receptors contributing to embryonic neuronal mo

101 Activation (affinity regulation) of integrin adhesion receptors controls cell migration and extracell

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

103 Selectins are a family of adhesion receptors designed for efficient leukocyte teth

104 approximately 45 min period during which the adhesion receptors did not respond to a second applicati

105 Since loss of the astrocyte adhesion receptor dystroglycan has been associated with

106 The adhesion receptor E-cadherin maintains cell-cell junctio

107 s in endothelial expression of the leukocyte adhesion receptor E-selectin and in microvascular leukoc

108 them to the Hippo pathway, whereas the cell-adhesion receptor Echinoid evolved as a new protein.

109 nclude members of the integrin family of ECM adhesion receptors, ECM proteins such as Wnts and latent

110 buted to adhesion, it is understandable that adhesion receptor engagement has been reported to alter

111 mig-38 and ina-1, which encodes an integrin adhesion receptor, enhanced the loss of turning phenotyp

112 lung metastatic capability in vivo The cell adhesion receptor EphA4 was determined to be a direct ta

113 oupling is usually mediated by transmembrane adhesion receptors, especially those of the integrin fam

114 rins are abundant heterodimeric cell-surface adhesion receptors essential in multicellular organisms.

115 to our knowledge the first example of a cell adhesion receptor exhibiting retrograde nuclear traffick

116 Although adhesion receptors expressed by CD4(+) T cells in the ge

117 PDK1 determines the cohort of chemokine and adhesion receptors expressed by PTEN-null cells, thereby

118 itate metastasis through binding to selectin adhesion receptors expressed on platelets, leukocytes an

119 Integrins are cell adhesion receptors, expressed on every cell type, that h

120 ll adhesion molecule-1, while characterizing adhesion receptor expression and topography on captured

121 monocyte subset as a function of changes in adhesion receptor expression using flow cytometric quant

122 ction, and by direct modulation of leukocyte adhesion receptor expression.

123 el with a transient reduction in endothelial adhesion receptor expression.

124 ial cells in vitro by inhibiting endothelial adhesion receptor expression.

125 ntified through the investigation of altered adhesion receptor expression.

126 lipase C pathway or the hindrance of surface adhesion receptors failed to impede PLT anti-S. aureus r

127 either the transmembrane isoform of the cell adhesion receptor fasciclin II (TM-MFas II) or the glyco

128 ults support a model where the engagement of adhesion receptors first activates talin or alpha-actini

129 ha-actinin with actin filaments and integrin adhesion receptors, fluorescence recovery after photoble

130 tactic factor or as a transmembrane-anchored adhesion receptor for circulating leukocytes.

131 (very late antigen-1; CD49a/CD29) is a major adhesion receptor for collagen I, IV, and VI, and its in

132 CD44, the leukocyte adhesion receptor for hyaluronan, has been considered a

133 ntegrin alpha6beta4 is an essential, dynamic adhesion receptor for laminin 332 found on epithelial ce

134 Integrin alpha3beta1 is a cell adhesion receptor for laminin-332/laminin-5 with importa

135 E-selectin, an endothelial cell surface adhesion receptor for leukocytes, also acts as a signali

136 onstrate the existence of a novel functional adhesion receptor for PS on the microendothelium that is

137 ns display carbohydrate facets that serve as adhesion receptors for cells including leukocytes and ba

138 is study adds to the classes of cell-surface adhesion receptors for FN and will help in the further c

139 L-SIGN), encode C-type lectins that serve as adhesion receptors for ICAM-2 and ICAM-3 and participate

140 collin 1 (Dsc1) is part of a desmosomal cell adhesion receptor formed in terminally differentiating k

141 The activation of integrin adhesion receptors from low to high affinity in response

142 The activation of heterodimeric integrin adhesion receptors from low to high affinity states occu

143 activation, the rapid conversion of integrin adhesion receptors from low to high affinity, occurs in

144 In mammals, beta1 integrin adhesion receptors generate signals that mediate cell sp

145 Moreover, targeting another platelet adhesion receptor, glycoprotein IIb/IIIa (GPIIb/IIIa), a

146 the glycoprotein (GP) Ibalpha subunit of the adhesion receptor GP Ib-IX.

147 genic growth factor, VEGF, and integrin cell adhesion receptors has emerged recently as a critical fa

148 sion efficiency, and lateral organization of adhesion receptors has not been established for any adhe

149 During inflammation, leukocytes bind to the adhesion receptors ICAM-1 and VCAM-1 on the endothelial

150 ng PDA, however, a causal role for this cell adhesion receptor in disease progression has yet to be d

151 important signaling receptor rather than an adhesion receptor in vivo and therefore promote beta1 in

152 Integrins are important adhesion receptors in all Metazoa that transmit conforma

153 which these molecules interact with integrin adhesion receptors in and outside the neuronal tissues.

154 The function of adhesion receptors in both cell adhesion and migration d

155 Expression of matrix adhesion receptors in brain microvessels decreases in is

156 urn, increases sialylation of beta1 integrin adhesion receptors in colon epithelial cells.

157 efects, we investigated the role of platelet adhesion receptors in stabilizing tumor vessels.

158 The membrane-proximal functions of adhesion receptors in turn trigger distal processes with

159 pillary venules and requires a unique set of adhesion receptors including peripheral node addressin,

160 M cells express high levels of chemokine and adhesion receptors, including CXCR4 and VLA-4.

161 The adhesion receptor integrin alpha(D)beta(2) promotes the

162 Expression of adhesion receptor integrin alphavbeta3 in an activated f

163 ecific for the activated conformation of the adhesion receptor integrin alphavbeta3 that is associate

164 of paired microbubbles targeted to the cell adhesion receptor integrin.

165 surface levels of the progression-associated adhesion receptors integrin alpha2beta1 and CD44 were di

166 n of the ligand binding affinity of integrin adhesion receptors (integrin activation) depends on the

167 ding model by showing that the main podocyte adhesion receptor, integrin alpha3beta1, interacts with

168 molecular abnormalities in a major platelet adhesion receptor, integrin alphaIIbbeta3.

169 CN1 induces fibroblast apoptosis through its adhesion receptors, integrin alpha6beta1 and the heparan

170 This involves factors such as the cell adhesion receptors integrins and amino acid transporters

171 ls sense the extracellular environment using adhesion receptors (integrins) linked to the intracellul

172 In their roles as major adhesion receptors, integrins signal across the plasma m

173 from peptide growth factors and the cellular adhesion receptors, integrins.

174 , leading to expression of the key leukocyte adhesion receptors intercellular adhesion molecule 1 (IC

175 ry late antigen-4 (VLA-4), CD49d/CD29) is an adhesion receptor involved in the interaction of lymphoc

176 llular cell adhesion molecule 1 (ICAM-1), an adhesion receptor involved in the recruitment of leukocy

177 Integrins are a large family of cell adhesion receptors involved in a variety of cellular fun

178 Integrins are cell membrane adhesion receptors involved in morphogenesis, immunity,

179 Regarding the adhesion receptors involved in TEM, alpha4 (most likely

180 The alpha4 integrin adhesion receptor is associated with enhanced protrusive

181 al by the EGFR and extracellular matrix/cell adhesion receptors is enabled, in part, by shared signal

182 The selectin family of leukocyte adhesion receptors is principally recognized for mediati

183 ed member of the beta2 subfamily of integrin adhesion receptors, is up-regulated on macrophage foam c

184 The adhesion receptors known as integrins perform key functi

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

186 XCL)12, CXCL13, and CCL19, and expression of adhesion receptors L-selectin, alpha(4)beta(7), and CLA.

187 ax to most chemokines and do not express the adhesion receptors L-selectin, alpha(4)beta(7), and cuta

188 The transmembrane neural cell adhesion receptor L1 is a Wnt/beta-catenin target gene e

189 lls with an antibody against the erythrocyte adhesion receptor Landsteiner-Wiener (intercellular adhe

190 This, along with engagement of adhesion receptors, leads to the formation of a speciali

191 integrins with cognate immunoglobulin class adhesion receptor ligands is an effective neuroprotectiv

192 s such as cells migrating along gradients of adhesion receptor ligands vs. any soluble cue.

193 efined mechanical properties and coated with adhesion receptor ligands.

194 MC activation was induced via at least 2 RBC adhesion receptors, LW and CD44.

195 ic domains (tails) of heterodimeric integrin adhesion receptors mediate integrins' biological functio

196 alin, to the cytoplasmic domains of integrin adhesion receptors mediates bidirectional signal transdu

197 pattern recognition receptor but also as an adhesion receptor mediating clustering between LCs and d

198 identified integrin alphaMbeta2 as the major adhesion receptor mediating monocyte adhesion to CCN1 an

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

200 In the course of studies to investigate the adhesion receptors mediating sickle RBC-WBC interactions

201 bilayers of protein clusters containing the adhesion receptor Nephrin and its cytoplasmic partners,

202 Spatial segregation of the antigen and adhesion receptors occurs within seconds of contact, cen

203 hesion cascade involving interaction between adhesion receptors of endothelial cells and ligands on C

204 Integrins are the major adhesion receptors of leukocytes and platelets.

205 " signaling through alphaIIbbeta3, the major adhesion receptor on the platelet surface.

206 s are mediated by upregulated selectin-class adhesion receptors on endothelial cells.

207 Activation of the integrin family of cell adhesion receptors on progenitor cells may be a viable a

208 Probing adhesion receptors on strategically engineered cells wit

209 addition to its regulating the expression of adhesion receptors on the yeast, we have found that hemo

210 ular matrix may be engaged in proteolysis of adhesion receptors on tumor cell surfaces.

211 in that it does not depend on major platelet adhesion receptors or GPCR signaling.

212 n) is a promiscuous ligand for numerous cell adhesion receptors or integrins.

213 cally engineered mice lacking major platelet adhesion receptors or their activators (alphaIIbbeta3, g

214 DLN T cells expressing binding sites for the adhesion receptor P-selectin (Plig(high) T cells) produc

215 pressure causes exocytosis of the leukocyte adhesion receptor P-selectin in endothelial cells (ECs),

216 trusions, known as knobs, where the parasite adhesion receptor P. falciparum erythrocyte membrane pro

217 th those elicited by the inhibitory platelet adhesion receptor PECAM-1 (platelet endothelial cell adh

218 This dual role for a cell adhesion receptor permits the cell to functionally conne

219 The beta1-integrin adhesion receptor plays a role in the regulation of cell

220 On the intracellular face of these linkages, adhesion receptors - principally integrins and syndecans

221 Mechanical forces acting on cell adhesion receptor proteins regulate a range of cellular

222 Heterodimeric integrin adhesion receptors regulate cell migration, survival and

223 Hetero-dimeric integrin adhesion receptors regulate cell migration, survival, an

224 Heterodimeric integrin adhesion receptors regulate diverse biological processes

225 ted contractility, membrane trafficking, and adhesion receptor remodeling.

226 s interactions between surface Neph1/nephrin adhesion receptors Roughest and Hibris, which bind the a

227 However, the CD47-activated SS RBC adhesion receptor(s) that mediated adhesion to immobiliz

228 us and mating type minus gametes mediated by adhesion receptors SAG1 and SAD1 activate a ciliary sign

229 eractions of this protein with its different adhesion receptors, Sag1 and Fig2p, a property of many h

230 s their constitutive expression of the viral adhesion receptor Siglec-1.

231 A substrate fusion protein composed of yeast adhesion receptor subunit Aga2, selection and countersel

232 ts establish that genetic differences in the adhesion receptor subunits alpha(2), alpha(IIb,) and GPV

233 posure to GM-CSF followed by the ligation of adhesion receptors such as CD44, CD11b, CD18, or CD15.

234 Some of these domains bind adhesion receptors such as integrins that mediate cell-m

235 -endothelial migration (TEM), leukocytes use adhesion receptors such as intercellular adhesion molecu

236 rimary cause of breast cancer mortality, and adhesion receptors, such as CD44, are believed to be cri

237 Transmembrane adhesion receptors, such as integrins, mediate cell adhe

238 3, a marker of mature dendritic cells, is an adhesion receptor that binds to resting monocytes and a

239 bbeta3 is a transmembrane (TM) heterodimeric adhesion receptor that exists in equilibrium between res

240 E-cadherin, an intercellular N-glycoprotein adhesion receptor that functions in the assembly of mult

241 -1, also called TMIGD2) gene as a novel cell adhesion receptor that is expressed in various human org

242 tercellular adhesion molecule-1 (ICAM-1), an adhesion receptor that mediates inflammatory and immune

243 Integrin CD11b/CD18 is a key adhesion receptor that mediates leukocyte migration and

244 CD44 can function as an adhesion receptor that mediates leukocyte rolling on hya

245 ntigen 1 (LFA-1; CD11a/CD18) is a key T cell adhesion receptor that mediates stable interactions with

246 rker CEACAM6, a highly abundant cell surface adhesion receptor that modulates the extracellular matri

247 ta1 integrin, CD49d/CD29) is a transmembrane adhesion receptor that plays an important role in cancer

248 ed whether microendothelial cells express an adhesion receptor that recognizes cell surface-expressed

249 Integrins are cell surface adhesion receptors that are essential for the developmen

250 The integrins make up a large family of cell adhesion receptors that are known to mediate bidirection

251 n and trafficking.Integrins are cell-surface adhesion receptors that are modulated by endo-exocytic t

252 Integrins are transmembrane adhesion receptors that bind extracellular matrix (ECM)

253 Integrins are cell-surface adhesion receptors that bind to extracellular matrices (

254 Integrins are cell adhesion receptors that communicate biochemical and mech

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

256 eterodimeric alpha/beta extracellular matrix adhesion receptors that couple physically to the actin c

257 stimuli would lead to surface expression of adhesion receptors that facilitate the binding of circul

258 Knowledge of the adhesion receptors that hES cells employ to engage extra

259 gnaling kinase cascade typically employed by adhesion receptors that involves upstream Src and FAK fa

260 Integrins are the major family of cell adhesion receptors that mediate cell adhesion to the ext

261 es of 24 alphabeta heterodimer transmembrane adhesion receptors that mediate cell-cell and cell-extra

262 Integrins are cell adhesion receptors that mediate cell-to-cell, or cell-to

263 Integrins comprise a large family of cell adhesion receptors that mediate diverse biological event

264 Integrins are cell-adhesion receptors that mediate interactions of cells wi

265 Integrins are the principal cell adhesion receptors that mediate leukocyte migration and

266 s are a family of heterodimeric (alpha+beta) adhesion receptors that play key roles in many cellular

267 Integrins are heterodimeric adhesion receptors that regulate immune cell adhesion.

268 staining for beta1 integrin, a component of adhesion receptors that regulate synapse maintenance and

269 ector molecules, and essential chemokine and adhesion receptors that regulate T cell trafficking.

270 Integrins are cell adhesion receptors that sense the extracellular matrix (

271 ukocyte)-selectin (CD62L) and CD44 are major adhesion receptors that support the rolling of leukocyte

272 Integrins are adhesion receptors that transmit force across the plasma

273 Integrins are a family of heterodimeric adhesion receptors that transmit signals bi-directionall

274 oting antigenic polymorphisms and/or diverse adhesions-receptors that may be involved in immune evasi

275 The platelet adhesion receptor, the glycoprotein Ib-IX-V complex, not

276 l-cell adhesion by interacting with cadherin adhesion receptors through beta-catenin, but the mechani

277 ned suggest that sadA is the first substrate adhesion receptor to be identified in Dictyostelium.

278 ronment and use the high-affinity form of an adhesion receptor to grow and secure host support for pr

279 ed the functional relationship between these adhesion receptors to determine how it regulates cell tr

280 Binding of integrin adhesion receptors to extracellular matrix components, s

281 atelets and show that adherent platelets use adhesion receptors to mechanically probe the adhesive su

282 matrix while increasing the connectivity of adhesion receptors to the actin cytoskeleton.

283 vation, and the failure to recruit essential adhesion receptors to the membrane contact site formed w

284 The ability of integrin adhesion receptors to undergo rapid changes in affinity

285 ions of Astn1 and Astn2, such as in membrane adhesion, receptor trafficking, and planar polarity sign

286 Integrin adhesion receptors transduce bidirectional signals acros

287 Adhesion receptors transduce mechanical force bidirectio

288 Integrin cell-adhesion receptors transduce signals bidirectionally acr

289 Cell migration during wound healing requires adhesion receptor turnover to enable the formation and d

290 lasmic tails regulate activation of integrin adhesion receptors via clasping/unclasping of their memb

291 In contrast, affinity modulation of adhesion receptors was unaffected.

292 CR1 have been previously shown to bind viral adhesion receptors, we speculate that NKp46/NCR1 may be

293 The distribution of membrane lipid rafts and adhesion receptors were analyzed by imaging flow cytomet

294 antibodies to red blood cell and endothelial adhesion receptors were used in vitro and in vivo to pro

295 ity (WRAMP) structure, which integrates cell-adhesion receptors with F-actin and myosin to form a mic

296 ombi is mediated by interactions of platelet adhesion receptors with ligands on the injured endotheli

297 e cytoskeletal protein Talin1 links integrin adhesion receptors with the actin cytoskeleton.

298 is identified as the dominant staphylococcal adhesion receptor, with Fnbps playing a supporting role.

299 ptor-treated mice showed alterations in cell adhesion receptors, with reduced CXCR2 and increased CD6

300 ycosylated receptors, immune receptors, cell adhesion receptors, Wnt receptors, and receptor tyrosine