ライフサイエンスコーパス: adherence of @2 to

1 ese mutant DbpA proteins did not inhibit the adherence of B. burgdorferi to a decorin substrata, and

2 a cell surface protein, Als1p, that mediates adherence of Candida albicans to a variety of human subs

3 ria, these antibodies were found to decrease adherence of M. catarrhalis to A549 human lung cells by

4 MS to laminin and fibronectin and reduce the adherence of M. tb to A549 cells.

5 lack of UspA1 expression does not affect the adherence of strain O35E to A549 human lung cells or pri

6 ression of Msg protein resulted in increased adherence of yeast to A549 alveolar epithelial cells.

7 identify bacterial proteins that promote the adherence of S. aureus to AD corneocytes.

8 of band 3 completely inhibited the abnormal adherence of sickle cells to an endothelial monolayer in

9 ctivation and sulfated glycosaminoglycans in adherence of H. somnus to BBEC.

10 Adherence of bacteria to biotic or abiotic surfaces is a

11 ion and IL-6 secretion in BMSCs triggered by adherence of MM cells to BMSCs, suggesting that it can i

12 -6, insulin-like growth factor 1 (IGF-1), or adherence of MM cells to bone marrow stromal cells (BMSC

13 Adherence of MM cells to bone marrow stromal cells (BMSC

14 Finally, adherence of MM cells to bone marrow stromal cells confe

15 insulin-like growth factor 1 (IGF-1), or by adherence of MM cells to bone marrow stromal cells.

16 bed Bap as the surface structure involved in adherence of A. baumannii to both normal human bronchial

17 dies, all of which significantly reduced the adherence of PMN to both control and cytokine-treated HP

18 lts suggest that OmpA and Lpp1 contribute to adherence of M. haemolytica to bovine respiratory epithe

19 copic analysis demonstrated that the initial adherence of S. typhimurium to Caco-2 cells in vitro inv

20 es with Caco2-BBE cells showed a decrease in adherence of EPEC to Caco2 cells in which CD98 expressio

21 icrovessels with "sludge." Other factors are adherence of cells to capillary and venular epithelial m

22 the absence of differences in either initial adherence of strains to cardiac valves or vegetation wei

23 dentified the region of PfEMP1 that mediates adherence of PE to CD36 and showed that a recombinant pr

24 Adherence of leukocytes to cells undergoing apoptosis ha

25 eport that this acquisition is due partly to adherence of prostasomes to cells and partly to a second

26 ethylcellulose (CMC) to assays decreased the adherence of the bacterium to cellulose.

27 In addition, we examined the adherence of leukocytes to cerebral venular endothelium

28 MAb 8E7 inhibited the adherence of strain O35E to Chang conjunctival epithelia

29 in 035E indicated that UspA1 was involved in adherence of this organism to Chang conjunctival epithel

30 Biofilm formation and adherence of V.parahaemolyticus to chitin is mediated by

31 synthetic peptides revealed the preferential adherence of lunasin to chromatin.

32 Ms) are bacterial surface proteins mediating adherence of the microbes to components of the extracell

33 Different degrees of adherence of mucins to contact lenses may occur, either

34 fection is thought to depend upon an initial adherence of the bacteria to corneal cells.

35 imal chain length required for the efficient adherence of IRBCs to CSPG and two 4-sulfated disacchari

36 Adherence of Helicobacter pylori to cultured gastric epi

37 Adherence of N. gonorrhoeae to cultured HEC-1-B cells wa

38 We hypothesize that adherence of GBS to cytokeratin may be important for mai

39 nized epithelium, such as the vagina, or for adherence of these bacteria to damaged epithelial cells

40 -EC interaction, whereas L1CAM increases the adherence of BrCa cells to ECs.

41 beta(2) integrins, which mediated increased adherence of BMDACs to endothelial cells.

42 nd that Als1p mediates both flocculation and adherence of C. albicans to endothelial cells in vitro.

43 Whether CAD1/AAF1 contributes to the adherence of C. albicans to endothelial cells remains to

44 treated with IL-10, a consistent increase in adherence of HL-60 to endothelial cells is observed.

45 known to activate integrins, also increased adherence of sickle erythrocytes to endothelial cells vi

46 The adherence of this clone to endothelial cells was over 10

47 n protein plays a critical role in mediating adherence of leukocytes to endothelium at sites of infla

48 Adherence of red cells to endothelium was quantified by

49 demonstrating that NanI is important for the adherence of C. perfringens to enterocyte-like cells, Na

50 ike FHA, however, FhaS was unable to mediate adherence of B. bronchiseptica to epithelial cell lines

51 Oligosaccharides that block the adherence of bacteria to epithelial cells in vitro--lact

52 l factor (Efa1) has been reported to mediate adherence of E. coli to epithelial cells.

53 The adherence of fimbrillin to epithelial cells was detected

54 We previously showed that adherence of gonococci to epithelial cells results in ch

55 tion of rpoH expression is not necessary for adherence of gonococci to epithelial cells, it is import

56 he putative EtpB transporter participates in adherence of H10407 to epithelial cells, thereby expandi

57 Adherence of Haemophilus influenzae to epithelial cells

58 tudies, there was no contribution of NanA to adherence of S. pneumoniae to epithelial cells or coloni

59 y the lipopolysaccharide O side chain in the adherence of this organism to epithelial cells are not u

60 re, human CR1 expression enhances the immune adherence of opsonized pneumococci to erythrocytes in vi

61 C4 deposition on WU2 and enhanced the immune adherence of WU2 to erythrocytes.

62 magglutinin (FHA) and pertactin, mediate the adherence of the bacterium to eukaryotic cells through v

63 Adherence of cells to fibronectin dramatically enhanced

64 Adherence of chondrocytes to fibronectin enhanced proteo

65 ectin and antifibronectin antibody inhibited adherence of conidia to fibronectin in the plate adheren

66 ese results demonstrate that Fnm affects the adherence of E. faecium to fibronectin and is important

67 As with PMN, adherence of EOS to fibronectin for 120 min caused nucle

68 lso transiently tyrosine-phosphoryated after adherence of these cells to fibronectin.

69 yrosine phosphorylation is induced following adherence of trypsinized fibroblasts to fibronectin or p

70 ic ulceration and distal gastric cancer, and adherence of H. pylori to gastric epithelial cells is cr

71 gastric adenocarcinoma, a process for which adherence of H. pylori to gastric epithelial cells is cr

72 Adherence of H. pylori to gastric epithelial cells seems

73 n serum albumin conjugate not only inhibited adherence of H. pylori to gastric epithelium but also di

74 L. jensenii inhibited the adherence of gonococci to glutaraldehyde-fixed epithelia

75 The intimin-specific antisera also blocked adherence of EHEC to HEp-2 cells.

76 We observed that the adherence of EPEC strains to HEp-2 cells was reduced and

77 hown previously by our laboratory to inhibit adherence of this strain to HEp-2 cells.

78 f Escherichia coli was found to increase the adherence of recombinant bacteria to HEp2 monolayers by

79 Adherence of Candida albicans to host tissues is a neces

80 The adherence of Candida glabrata to host cells is mediated,

81 hypothesis that StcE contributes to intimate adherence of EHEC to host cells by cleavage of glycoprot

82 The hmwABC locus promotes adherence of H. influenzae to host cells.

83 plexes and is highly effective in inhibiting adherence of P. gingivalis to host cells.

84 aminase 2 (TG2) plays a critical role in the adherence of P. gingivalis to host cells.

85 The adherence of Porphyromonas gingivalis to host cells is l

86 A therapeutic approach to block or reverse adherence of PRBCs to host cell receptors can now be pur

87 try process and that Sca1 is involved in the adherence of R. conorii to host cells.

88 Adherence of Staphylococcus aureus to host tissues is a

89 g mucosal surfaces of the respiratory tract; adherence of the bacteria to host cells is presumed to b

90 adhesive matrix molecules) that mediate the adherence of the bacteria to host extracellular matrix c

91 The adherence of the organism to host epithelium signals cha

92 isease processes follow the initial steps of adherence of the organism to host tissues and subsequent

93 i (EHEC) O157:H7 and contributes to intimate adherence of this bacterium to host cells, a process ess

94 ression is both necessary and sufficient for adherence of vegetative forms to host cells.

95 The adherence of PMN to HPMC after stimulation with either I

96 N counter receptor LFA-1 (CD11a/CD18) in the adherence of PMN to HPMC were confirmed by using anti-CA

97 Deletion of this adhesin reduced adherence of C. glabrata to human epithelial cells by 95

98 aA-type pilus is sufficient for the specific adherence of corynebacteria to human pharyngeal epitheli

99 Deletion of csrA resulted in decreased adherence of H. ducreyi to human foreskin fibroblasts (H

100 presented here, therefore, investigates the adherence of human PMN to human peritoneal mesothelial c

101 o M.tb and the effect of this binding on the adherence of M. tb to human macrophages.

102 mediate C'-dependent killing and to inhibit adherence of NTHI strains to human oropharyngeal cells.

103 ermine the role of hemagglutinin B (HagB) in adherence of P. gingivalis to human coronary artery endo

104 esults indicate that HagB is involved in the adherence of P. gingivalis to human primary endothelial

105 interaction of PspC with FH may also mediate adherence of pneumococci to human cells.

106 Adherence of pneumococci to human-derived cells was asse

107 nce upon sialylated carbohydrate ligands for adherence of S. pneumoniae to human upper airway epithel

108 he bovine aortic ECs, hypoxia stimulated the adherence of sickle RBCs to human retinal capillary ECs,

109 gaA and NanA were shown to contribute to the adherence of unencapsulated pneumococci, to human epithe

110 e B. anthracis envelope factor that mediates adherence of vegetative forms to human cells and isolate

111 Beta 1-integrin function was determined by adherence of fibronectin beads to IEC-6 monolayers.

112 t the B domain significantly reduce in vitro adherence of S. epidermidis to immobilized collagen.

113 om immunized mice for the ability to inhibit adherence of S. mutans to immobilized human salivary agg

114 These items address whether and how adherence of participants to interventions is assessed o

115 -encoded virulence proteins that promote the adherence of O157 to intestinal epithelial cells and the

116 Intimate adherence of the bacteria to intestinal epithelial cells

117 mation is initiated almost immediately after adherence of V. cholerae to intestinal cells.

118 hat SPR is an efficient method for measuring adherence of a toxin to isolated cell plasma membranes.

119 these organisms has been correlated with the adherence of bacteria to isolated enterocyte brush borde

120 Anti-SdrF antibodies reduced adherence of S. epidermidis to keratin and keratinocytes

121 e determinant and has been implicated in the adherence of H. ducreyi to keratinocytes.

122 This is the first report of in vitro adherence of S. pyogenes to keratinocytes in a manner th

123 fixed epithelial cells like it inhibited the adherence of gonococci to live epithelial cells, suggest

124 Adherence of PMN to Ln decreased IL-1 beta types I, II r

125 Together, these results indicate that the adherence of Pc to lung matrix proteins and epithelial c

126 localizes to the cell wall and enhances the adherence of the bacteria to lung epithelial A549 cells.

127 long polar fimbriae (Lpf), which facilitate adherence of S Typhimurium to M cells.

128 In contrast to internalization, adherence of DU5883 to MAC-T was reduced by only approxi

129 ting concentrations of SP-D leads to reduced adherence of the bacteria to macrophages (62.7% of contr

130 lectin has been shown previously to mediate adherence of E. histolytica to mammalian epithelial cell

131 ction of IL-8 and MCP-1 also did not require adherence of bacteria to meningeal cells, but LPS was im

132 otein 1 (PfEMP1) family proteins mediate the adherence of infected erythrocytes to microvascular endo

133 Adherence of sickle erythrocytes to microvascular endoth

134 in reduced internalization without affecting adherence of bacteria to monocytes.

135 w Chlamydia pneumoniae infection affects the adherence of GFP-macrophages to mouse endothelial cells

136 Cell surface macromolecules are critical for adherence of commensal bacteria to mucus but structural

137 esion molecule expression resulted in weaker adherence of T cells to NOD-Idd22 endothelium compared w

138 There was limited adherence of control bubbles to normal or activated ECs,

139 Adherence of C. albicans to oral epithelial cells was un

140 dies provide evidence that FimA mediates the adherence of P. gingivalis to oral epithelial cells.

141 idative load such as those that occur during adherence of erythrocytes to phagocytes.

142 tein were able to decrease significantly the adherence of streptococci to pharyngeal cells.

143 x molecules (MSCRAMMs) Ace and Fss2, mediate adherence of E. faecalis to platelets.

144 utologous plasma significantly increased the adherence of SS-RBC to PMN but had no effect on AA-RBC (

145 The adherence of neutrophils to postexperimental coronary ar

146 to ligated rabbit ileal loops, decreased the adherence of EPEC to rabbit ileum, and reduced histopath

147 and antiserum to these proteins reduced the adherence of B. hermsii to red blood cells.

148 Adherence of Haemophilus influenzae to respiratory epith

149 ociated molecules, which are involved in the adherence of the organism to respiratory epithelial cell

150 aureus have previously been shown to mediate adherence of the organism to resting endothelial cells i

151 26 amino acids is sufficient to mediate the adherence of P. gingivalis to S. gordonii and that the s

152 and suggested its importance in the initial adherence of S. mutans to saliva-coated tooth surfaces a

153 that P1 expression is necessary for in vitro adherence of S. mutans to salivary agglutinin-coated hyd

154 ared the contribution of GspB and Hsa to the adherence of S. gordonii to selected glycoproteins.

155 Adherence of mycoplasmas to specific tissue surfaces is

156 tential importance of integrins in mediating adherence of SPCs to specific ECM both in vitro and in v

157 VQDLLKK and NITVK motif and suggest that the adherence of P. gingivalis to streptococci is driven by

158 ITVK active region of BAR that increased the adherence of P. gingivalis to streptococci.

159 lose-binding protein that may be involved in adherence of R. albus to substrate and extends understan

160 ow that the tad genes are required for tight adherence of A. actinomycetemcomitans to surfaces and ar

161 es, which are required for tight nonspecific adherence of A. actinomycetemcomitans to surfaces, cause

162 ocus of seven genes required for nonspecific adherence of A. actinomycetemcomitans to surfaces.

163 Histologic examination revealed close adherence of bacteria to the intestinal epithelium in th

164 This study indicates that the adherence of bacteria to the intestinal mucosal surface

165 with the growth of pathogens and the greater adherence of bacterial pathogens to the oral mucosa are

166 well as the INT1 gene product, to influence adherence of Candida albicans to the intestinal epitheli

167 Both conditions have in common the adherence of cortical vitreous to the inner layer of per

168 r solubilization in surfactant micelles) and adherence of graft-polymer to the membrane surface, whic

169 Adherence of Helicobacter pylori to the gastric epitheli

170 Adherence of Helicobacter pylori to the gastric epitheli

171 There is, in addition, a striking adherence of Inr sequences to the Inr consensus in DPE-c

172 f MDCK cell monolayers also greatly enhances adherence of J96 to the apical surface of the cell monol

173 Further, the adherence of leukocytes to the endothelium appeared to b

174 platelet adherence and aggregation, reduces adherence of leukocytes to the endothelium, and suppress

175 of diabetic retinopathy is the inappropriate adherence of leukocytes to the retinal capillaries.

176 ANCA act in concert with chemokines to cause adherence of leukocytes to the walls of small vessels wi

177 ell death was contact dependent and required adherence of live bacteria to the host cell.

178 Adherence of lymphocytes to the fungus is the first step

179 The disease process is initiated by adherence of M. hyopneumoniae to the cilia of swine resp

180 the pathogenesis of atherosclerosis, and the adherence of monocytes to the arterial endothelium is on

181 echanism by which C. pneumoniae promotes the adherence of mononuclear phagocytes to the endothelium a

182 Adherence of Mycoplasma hyopneumoniae to the swine respi

183 tion is controlled, at least in part, by the adherence of myelin sheaths to the axolemma in the adjac

184 ONOO- also significantly reduced adherence of neutrophils to the ischemic-reperfused LAD

185 traumatic shock is associated with increased adherence of neutrophils to the vascular endothelium res

186 The adherence of Opa+ GC to the neutrophils can be enhanced

187 th Neisseria gonorrhoeae 1291 Opa+ P+ showed adherence of organisms to the epithelial cell membrane,

188 intra-alveolar aggregation of organisms and adherence of P. carinii to the lung epithelium.

189 a significant dose-dependent increase of the adherence of P. carinii to the macrophages.

190 Transmission begins with the adherence of P. luminescens to the rectal gland cells (R

191 tiadhesive activity and directly inhibit the adherence of pathogens to the host epithelial cell surfa

192 This interaction initiates the adherence of platelets to the subendothelial vasculature

193 Adherence of platelets to the surface of smooth muscle c

194 To study the adherence of rheumatologists to the hydroxychloroquine (

195 To study carbohydrate-mediated adherence of Streptococcus pneumoniae to the human airwa

196 types of epithelial cells and may facilitate adherence of the bacteria to the bladder epithelium.

197 activates the receptor that allows tenacious adherence of the bacteria to the host cell surface.

198 Localization and adherence of the biofilm to the flea foregut is essentia

199 nslocated intimin receptor) to promote tight adherence of the organism to the host-cell plasma membra

200 We evaluated the rate of adherence of the participants to the screening protocol,

201 cules, culminating in rolling and subsequent adherence of these cells to the vascular wall.

202 for the combinatorial method comes from the adherence of these complexes to the energy gap law.

203 Adherence of transplanted cells to the hepatic endotheli

204 Latex bead treatment did not affect adherence of trophozoites to the corneal epithelium or p

205 gene vpsT was observed within 30 minutes of adherence of V. cholerae to the intestinal cell line INT

206 ifferent biological kingdoms, suggesting the adherence of P450s to their innate function such as thei

207 purified and structurally characterized, and adherence of IRBCs to these CSPGs investigated.

208 lts imply that another molecule mediates the adherence of M. catarrhalis to these two cell lines.

209 In this report we demonstrate that the flow adherence of sickle cells to thrombin-treated human vasc

210 oli O157:H7 (EHEC), is required for intimate adherence of these organisms to tissue culture cells and

211 Adherence of enveloped virions to unrecycled viral prote

212 es performed 20 years ago revealed increased adherence of sickle erythrocytes to vascular endothelial

213 The adherence of sickle erythrocytes to vascular endothelium

214 and neither GAPDH nor MAb ws1 inhibited the adherence of trichomonads to VECs.

215 taNA) had no effect on NA activity or on the adherence of S. pneumoniae to virus-infected human alveo

216 Adherence of PKCdelta EC to vitronectin was significantl

217 xogenous recombinant StcE increased intimate adherence of the mutant to wild-type levels.