ライフサイエンスコーパス: cell adherence

1 ued O-linked glycosylation of E-cadherin and cell adherence.

2 eved its inhibitory effect on GAS pharyngeal cell adherence.

3 CS increased both biofilm formation and host cell adherence.

4 poly(2-hydroxyethyl methacrylate) to control cell adherence.

5 ression, transformation efficiency, and host cell adherence.

6 g that PilQ may be directly involved in host cell adherence.

7 nd then coated with polylysine to facilitate cell adherence.

8 is not dependent on, but is compatible with, cell adherence.

9 iral activities as well as the modulation of cell adherence.

10 gative with respect to aggregation and human cell adherence.

11 tate the further study of the phenomena of M-cell adherence.

12 ion, twitching motility and human epithelial cell adherence.

13 tive effect on extracellular lectin-mediated cell adherence.

14 DNA transformation efficiency and epithelial cell adherence.

15 04, and 118.1) shown to block Mac-1-mediated cell adherence.

16 sses AF/R1 pili that mediate Peyer's patch M-cell adherence.

17 he degree to which inhibition of the corneal cell adherence affects the course of infection and disea

18 in intrageneric coaggregations, the cell-to-cell adherence among genetically distinct streptococci.

19 e adhesive glucans, which facilitate cell-to-cell adherence and accumulation.

20 lular matrix protein fibronectin resulted in cell adherence and allowed detection of cellular respons

21 ers cell migration and invasion by promoting cell adherence and by inhibiting cell movement.

22 le in the interaction with alpha 4 beta 7 in cell adherence and cell activation.

23 M1 protein-Fg binding reduces GAS pharyngeal cell adherence and colonization in a fashion that is cou

24 m and secreted putrescine are linked to host cell adherence and cytotoxicity.

25 ll-established roles in mediating epithelial cell adherence and DNA transformation.

26 Enterococcus faecalisis associated with host cell adherence and endocarditis.

27 inues the cascade of events, which increases cell adherence and infiltration of the organ.

28 growth rate, motility, secretion and INT 407 cell adherence and internalization assays.

29 esicles (OMVs) could modulate the epithelial cell adherence and invasion abilities of T. forsythia.

30 age survival assay, an intestinal epithelial cell adherence and invasion assay, and the calf model of

31 erefore undertaken to address the epithelial cell adherence and invasion properties of T. forsythia a

32 iophysical cues to direct corneal epithelial cell adherence and migration.

33 for CrgA in virulence regulation during both cell adherence and planktonic growth.

34 ly transparent path to visualize endothelial cell adherence and supports integration of removable ele

35 d a gravity displacement assay for examining cell adherence and used it to quantitatively monitor the

36 of islet architecture (specifically cell-to-cell adherence) and a decrease in coordinate function (e

37 ntributes to plasmid conjugation, epithelial cell adherence, and adherence to abiotic surfaces.

38 of the genes controlling inducible cytokine, cell adherence, and antiviral programs.

39 tact during chemotropic interactions, during cell adherence, and postfusion by triggering programmed

40 rythrocyte agglutination, explanted tracheal cell adherence, and turkey poult tracheal colonization.

41 proteins was evaluated using a radiolabeled-cell adherence assay.

42 borated with similar results from the Caco-2 cell adherence assay.

43 ay described here and by a polymorphonuclear cell adherence assay.

44 ggregative Escherichia coli (EAggEc) by HeLa cell adherence assay.

45 ach mutant was judged by performing in vitro cell adherence assays with chicken LMH hepatocellular ca

46 potent than native LXA4 in stimulating THP-1 cell adherence, at subnanomolar concentrations.

47 tein expression is induced during epithelial-cell adherence, bfpA-cat transcriptional fusions and nor

48 em (TadSS) assembles surface pili that drive cell adherence, biofilm formation and bacterial predatio

49 We investigated the role of YDF in cell adherence, biofilm formation, colonization of spina

50 Epithelial cell adherence by the M1(-) strain, however, was unaffec

51 adhesins Als4112 and Scf1 in mediating cell-cell adherence, coaggregation and biofilm formation.

52 exhibited a fivefold increase in endothelial cell adherence, compared with S. cerevisiae transformed

53 This study revealed unique host cell adherence contacts, early endocytosis-specific stru

54 gens); it therefore plays important roles in cell adherence, development, and immunity.

55 r more potent than LXA4 in stimulating THP-1 cell adherence (EC50 approximately 1 x 10(-10) M).

56 containing hemagglutinating pili, epithelial cell adherence exhibited by these strains is not mediate

57 Untreated M1Egr-1 cells also exhibited cell adherence, expression of Fc and C3 receptors, and u

58 ctor of filamentation and also mediates cell-cell adherence (flocculation).

59 dly reduced effects on leukocyte-endothelial cell adherence in eNOS- and iNOS-deficient mice compared

60 nsplantation, specifically disrupted cell-to-cell adherence in islets through the actions of membrane

61 gulatory protein that stimulates endothelial cell adherence in S. cerevisiae by inducing a flocculati

62 ant role in mediating neutrophil-endothelial cell adherence in septic shock.

63 chemokine receptor 7 (CCR7), blocked T(GFP) cell adherence in wild-type HEVs, whereas desensitizatio

64 lus assembly and is implicated in epithelial cell adherence, in a soluble form.

65 body 4B5, or an RGD peptide inhibited sickle-cell adherence induced by PDBu.

66 onstrated that it was deficient in red-blood-cell adherence, induction of PS exposure, and phagocytos

67 demonstrated using MDA-MB-231 breast cancer cells adherence inhibition assay.

68 examined using isolated receptor binding and cell adherence/internalization assays.

69 autotransporters) that are critical for host cell adherence, invasion, and biofilm formation.

70 Sickle cell adherence involves several receptor-mediated proces

71 nhances the permeability of interendothelial cell adherence junctions in response to vascular endothe

72 duction and energy metabolism may coordinate cell adherence, local proteolysis, oxidant release, acti

73 The role of NanH in host epithelial cell adherence may be masked by the presence of a second

74 f genes related to progressive expression of cell adherence molecules, and cytokines and chemokines i

75 rge, complex, flexible structure involved in cell adherence, motility and cell division.

76 kines and proteases, cell cycle progression, cell adherence, motility and metabolism.

77 exogenously to specifically facilitate HEp-2 cell adherence of EHEC but not E. coli K-12.

78 NA transformation competence, and epithelial cell adherence of the gonococcus.

79 mponent and viral protein that mediate the M cell adherence of these viruses.

80 ype 86-24 to HEp-2 cells and conferred HEp-2 cell adherence on 86-24eaeDelta10, an eaeA deletion muta

81 ial for signaling for O-2 generation but not cell adherence or azurophil degranulation.

82 cause these surface proteins are involved in cell adherence or invasion during host infection, we als

83 , the maturation of the virus particle, cell-cell adherence, or Gag polarization and virological syna

84 r the yeast-hypha dimorphic transition, host cell adherence, or host cell injury, which are all estab

85 ysis of pilus assembly by TEM and epithelial cell adherence over a time course of induction demonstra

86 vere defects in E-cadherin cleavage, loss of cell adherence, paracellular transmigration, and basolat

87 n displayed a localized adherence-like HEp-2 cell adherence pattern, as seen in diarrheic human infan

88 DNA encoding virulence factors and the HEp-2 cell adherence patterns of Escherichia coli strains isol

89 ate other roles for alpha 4 beta 1 in sickle-cell adherence, the ability of activated alpha 4 beta 1

90 ntribution of each protein in bacterium-host cell adherence, the C. jejuni genes encoding the putativ

91 cculated and exhibited increased endothelial cell adherence, the relationship between adherence and f

92 tigated the effects of TNF-alpha on human NK cell adherence to and cytotoxicity of porcine aortic end

93 olysaccharide/adhesin (PS/A), which mediates cell adherence to biomaterials, and another antigen, ter

94 ide-adhesin (PS/A) that mediates the initial cell adherence to biomaterials.

95 abrogates IL-6 secretion triggered by tumor cell adherence to bone marrow stromal cells.

96 ted role in collagen cross-linking and tumor cell adherence to collagen.

97 d anti-CD54 blocked basal levels of Th1-type cell adherence to endothelial cells and also inhibited t

98 on were scored for endarteritis, mononuclear cell adherence to endothelial cells, endothelial activat

99 Sickle-cell adherence to endothelium has been hypothesized to i

100 st cells, CalDAG-GEF Ia expression increases cell adherence to fibronectin in response to PMA and cal

101 troglycan is critically important for muscle cell adherence to its surrounding matrix.

102 4 stimulated a concentration-dependent THP-1 cell adherence to laminin with concentrations as low as

103 activation of alpha4beta7 integrin promotes cell adherence to mucosal addressin cell adhesion molecu

104 The method was applied to examine tumor cell adherence to recombinant E-selectin.

105 t hematopoietic cell movement, and increased cell adherence to stroma.

106 me constitutively activated concomitant with cell adherence to the culture plates.

107 and T cells to examine V(beta)-restricted T cell adherence to the endothelial cell monolayer, V(beta

108 Mononuclear cell adherence to vascular endothelium and perivascular

109 ells by quantifying NF-kappaB activation and cell adherence was completed.

110 Cell adherence was greater than 60% of applied cells for

111 Limited uroepithelial cell adherence was observed in vivo, and weak D-mannose-

112 e importance of Flp1 in fibril formation and cell adherence, we used transposon IS903phikan to isolat

113 ithelial monolayers can promote inflammatory cell adherence which could, in turn, potentially contrib

114 nd that MSA treatments at 2 microM increased cell adherence, while inhibiting cell migration and tube

115 ant increases in aggregation and endothelial cell adherence with associated decreases in neutrophil r

116 n contrast, overexpression of HfsH increased cell adherence without increasing holdfast synthesis.