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 ress high levels of beta1 and beta2 integrin adhesion receptors.

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

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

11 herin would affect expression of cell matrix adhesion receptors.

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

13 1 and occupies the binding site for integrin adhesion receptors.

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

15 chronous sideways movement of beta1 integrin adhesion receptors.

16 sequence similarity to known matrix protein adhesion receptors.

17 substrates capable of engaging specific cell-adhesion receptors.

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

19 rease in the functional activity of integrin adhesion receptors.

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

21 al cooperativity between integrins and other adhesion receptors.

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

23 nderstanding the regulation of integrin cell adhesion receptors.

24 ell migration initiated by growth factor and adhesion receptors.

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

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

27 performed in animal models deficient in both adhesion receptors.

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

29 d to various chemotactic signals and express adhesion receptors.

30 ased expression of cell-cell and cell-matrix adhesion receptors.

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

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

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

34 othelial surface by altering the dynamics of adhesion receptors.

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

36 tly by inadequate expression of cell surface adhesion receptors.

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

38 Syk can also be activated by integrin adhesion receptors [4,5], but the mechanism of its activ

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 mplexity of interactions between MT1-MMP and adhesion receptors and suggest that regulation of integr

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

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

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

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

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

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

63 ends on integrins, a family of transmembrane adhesion receptors, and is regulated by integrin activat

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

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

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

67 Integrin adhesion receptors appear to be regulated by molecules t

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

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

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

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 This is particularly true for adhesion receptors because their function requires tight

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

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

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

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

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

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

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

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

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

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

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

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

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

88 It has become widely accepted that adhesion receptors can either directly activate, or sign

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

90 e effective affinity and kinetic rates of an adhesion receptor (CD16b) placed in three distinct envir

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

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

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

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

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

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

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

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

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

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

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

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

109 issues by means of an orderly progression of adhesion receptor engagements.

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

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

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

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

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

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

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

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

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

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

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

121 ntified through the investigation of altered adhesion receptor expression.

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

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

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

125 actions between members of the integrin cell adhesion receptor family and the extracellular matrix th

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

127 ct peripheral nervous system (PNS), the cell adhesion receptor fasciclin II has been shown to play a

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 eta(2) (Mac-1, CD11b/CD18) is a cell surface adhesion receptor for fibrinogen.

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

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

135 therefore to exocytosis of both P-selectin (adhesion receptor for leukocytes) and von Willebrand fac

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

137 ates that the alpha(4)beta(1) integrin is an adhesion receptor for OPN and that alpha(4)beta(1) bindi

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

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

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

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

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

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

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

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

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

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

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

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

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

151 Mel-CAM (MCAM, MUC 18, CD146) is a cell-cell adhesion receptor highly expressed by melanoma cells but

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

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

154 onal role of a melanoma-associated cell-cell adhesion receptor in tumor progression.

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

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

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

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

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

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

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

162 To determine the role of integrin adhesion receptors in T cell development, we have expres

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

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

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

166 mic properties of the cytosolic tails of the adhesion receptor integrin alphaIIbbeta3, fused to a coi

167 Expression of adhesion receptor integrin alphavbeta3 in an activated f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

185 The alpha4 integrin adhesion receptor is associated with enhanced protrusive

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

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

188 An important role of cell matrix adhesion receptors is to mediate transmembrane coupling

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

190 The adhesion receptors known as integrins perform key functi

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

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

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

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

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

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

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

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

199 efined mechanical properties and coated with adhesion receptor ligands.

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

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

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

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

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

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

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

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

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

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

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

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

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

213 Probing adhesion receptors on strategically engineered cells wit

214 es to inflamed tissue using cytokine-induced adhesion receptors on the surfaces of interacting cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

228 Heterodimeric integrin adhesion receptors regulate cell migration, survival and

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

230 Heterodimeric integrin adhesion receptors regulate diverse biological processes

231 The cell surface adhesion receptors required have not been identified.

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

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

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

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

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

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

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

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

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

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

242 3, a marker of mature dendritic cells, is an adhesion receptor that binds to resting monocytes and a

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

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

245 -1, also called TMIGD2) gene as a novel cell adhesion receptor that is expressed in various human org

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

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

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

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

250 surface tTG serves as an integrin-associated adhesion receptor that might be involved in extravasatio

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

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

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

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

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

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

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

258 Integrins are cell adhesion receptors that communicate biochemical and mech

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

274 Integrins are adhesion receptors that transmit force across the plasma

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

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

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

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

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

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

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

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

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

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

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

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

287 Integrin adhesion receptors transduce bidirectional signals acros

288 Adhesion receptors transduce mechanical force bidirectio

289 Integrin cell-adhesion receptors transduce signals bidirectionally acr

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

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

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

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

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

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

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

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

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

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

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