ライフサイエンスコーパス: adhesiveness

1 the most intense response to proteolysis and adhesiveness.

2 unction with increased leukocyte-endothelium adhesiveness.

3 turn arise from differences in intercellular adhesiveness.

4 second messenger that regulates cell surface adhesiveness.

5 bacteria enriched with magnesium had higher adhesiveness.

6 t did not affect FAK phosphorylation or cell adhesiveness.

7 nding sites, in turn, a consequence of their adhesiveness.

8 th positively and negatively affect cadherin adhesiveness.

9 tive magnitudes of homotypic and heterotypic adhesiveness.

10 cocytes from these mice did not show altered adhesiveness.

11 ectodomain alone significantly strengthened adhesiveness.

12 elix factor Hxt and acquisition of increased adhesiveness.

13 uch cells also exhibited increased cell-cell adhesiveness.

14 facilitates ligand interaction and increased adhesiveness.

15 e examined the role of band 3 in sickle cell adhesiveness.

16 ecifically CD7-induced increases in integrin adhesiveness.

17 y be related to down-regulation of leukocyte adhesiveness.

18 transfected with E-cadherin exhibited strong adhesiveness.

19 s to identify biomarkers for proteolysis and adhesiveness.

20 , but also to the downregulation of platelet adhesiveness.

21 antibody (mAb) significantly decreased cell adhesiveness.

22 n of ET-1 on thrombin-stimulated endothelial adhesiveness.

23 roteins essential for integrin-mediated cell adhesiveness.

24 ditional tissue-specific adaptations of cell adhesiveness.

25 f tissue adhesives with regard to colorectal adhesiveness.

26 n but also substrate rigidity, topology, and adhesiveness.

27 e strategies, at each extreme on the axis of adhesiveness.

28 ss, can compensate for the cost of increased adhesiveness.

29 g by ICOS-Fc inhibits human endothelial cell adhesiveness.

30 but partially conserved very late antigen-4 adhesiveness.

31 sing shRNAs led to changes in morphology and adhesiveness.

32 conformations and up-regulation of leukocyte adhesiveness.

33 RhoA activities and compromised cell-matrix adhesiveness.

34 volved in developmental progression to hyper-adhesiveness.

35 ndex had statistically significant increased adhesiveness.

36 its intrinsic transferability and universal adhesiveness.

37 g their proteolysis indices and instrumental adhesiveness.

38 , apparently because of their high levels of adhesiveness.

39 this nucleotide prevent swarming and promote adhesiveness.

40 y for soluble ligand correlate with cellular adhesiveness?

41 portant in the induction of endothelial cell adhesiveness, a prerequisite for the recruitment of circ

42 ion allows the growth cone to rapidly adjust adhesiveness across its axis, an essential feature for i

43 ol animals significantly increased leukocyte adhesiveness after shock and resuscitation.

44 are hyperreactive and demonstrate increased adhesiveness, aggregation, degranulation, and thrombus f

45 their appearance, growth/proliferation, and adhesiveness, although, as expected, they had reduced pl

46 ss, fragility, cohesiveness, springiness and adhesiveness and (iv) four structural parameters: fibre

47 knockdown of Trask results in increased cell adhesiveness and a failure to properly inactivate focal

48 progeny of this cell show reduction in cell adhesiveness and a rounded shape at the blastocyst stage

49 demonstrate that such particles show strong adhesiveness and aggregation, leading to a more diverse

50 rcinoma cell lines that displayed E-selectin adhesiveness and an increased metastatic capacity in cyt

51 ause sickle erythrocytes also show increased adhesiveness and because the membrane portion of band 3

52 ioventricular cardiomyocytes to promote cell adhesiveness and cell shapes during cardiac morphogenesi

53 A kinetic analysis for TVBN, SSP, hardness, adhesiveness and chewiness, was performed.

54 up of proteins, which play a key role in its adhesiveness and cohesiveness.

55 are shed into the medium and have decreased adhesiveness and cohesiveness.

56 ng dry-cured ham processing may lead to high adhesiveness and consumer dissatisfaction.

57 alaria surface proteins that reduce parasite adhesiveness and could reduce the risk of severe disease

58 e ventral epidermis, cells either lose their adhesiveness and fall out of the epidermis or undergo ap

59 rin-catenin complexes, resulting in enhanced adhesiveness and functional anchorage of initiated cells

60 requirement of the open LFA-1 headpiece for adhesiveness and high affinity.

61 ion was required for efficient OmpX-mediated adhesiveness and internalization but not serum resistanc

62 asin, as coating inert beads with it confers adhesiveness and invasiveness.

63 lts suggest that APP may have a role in cell adhesiveness and maturation of endothelial cells into ca

64 Their adhesiveness and migration to vitronectin or osteopontin

65 echanisms of negative regulation of integrin adhesiveness and neutrophil recruitment are poorly under

66 Because of the conflicting contributions of adhesiveness and other traits to movement within plants

67 Adhesiveness and proliferative potential were restored b

68 TCR-induced up-regulation of LFA-1-dependent adhesiveness and resulting T cell-APC conjugation requir

69 ith enhanced temporally controlled leukocyte adhesiveness and shape-changes promoting leukocyte attac

70 egative MAP kinase kinase 1 mutant decreased adhesiveness and stem cell number in the absence of CD8b

71 1 interactions themselves activate integrin adhesiveness and trigger transmigration--in some cases b

72 lting in compromised epithelial polarity and adhesiveness) and in kidney and heart (resulting in hypo

73 ilizes peripheral focal adhesions, increases adhesiveness, and decreases the rate of cell detachment.

74 uced cellular ruffles, loss of intercellular adhesiveness, and increased cell migration could be mimi

75 OmpX-mediated serum resistance, adhesiveness, and invasiveness, although dependent on LP

76 Surface beta1 integrin levels, adhesiveness, and mitogen-activated protein (MAP) kinase

77 PI3K and ERK/MAPK pathways, control of cell adhesiveness, and movement.

78 ompanied by decreased CD11b expression, cell adhesiveness, and phagocytosis.

79 atically enhances cellular survival, growth, adhesiveness, and resistance to heat and oxidative stres

80 es altered cell morphology and intercellular adhesiveness, and significantly decreased the number of

81 eded in cell lines with larger nuclei, lower adhesiveness, and to a lesser degree also in cells with

82 lved in leukocyte transmigration in that its adhesiveness appears to be regulated partly by rapid end

83 e whether high beta1 integrin expression and adhesiveness are essential for maintaining keratinocytes

84 er, the mechanisms underlying changes in its adhesiveness are poorly understood.

85 omes change from calcium-dependence to hyper-adhesiveness as blastocyst development proceeds from E3

86 mulated distal pericryptal sheath growth and adhesiveness as shown by increased amounts of F-actin, s

87 ade, mediates the sustained increase in cell adhesiveness associated with monocytic differentiation.

88 ant heterogeneity in cell wall stiffness and adhesiveness at the nm scale.

89 fects on intestinal epithelial cell movement/adhesiveness; augmentation of E-cadherin-beta-catenin co

90 Moreover, the difference in adhesiveness between calcium-dependent and calcium-indep

91 hocyte function-associated antigen 1 (LFA-1) adhesiveness by a previously unknown pathway that activa

92 tact cells, including activation of integrin adhesiveness by application of tensile force by the cyto

93 s biological activity of promoting cell-cell adhesiveness by inducing lateral dimerization of the ass

94 s junctions, which play a major role in cell adhesiveness by mediating calcium-dependent homophylic i

95 icating PI 3-K in the regulation of integrin adhesiveness by multiple cell surface signaling receptor

96 Since adhesiveness can be coupled to the strength of overlap,

97 Integrin adhesiveness can be dynamically regulated through a proc

98 electins, VLA-4 integrin-mediated lymphocyte adhesiveness can be modulated by chemokines through intr

99 physical properties including contractility, adhesiveness, cell stiffness, and nuclear volume.

100 rapid transition to an intermediate state of adhesiveness characterized by loss of actin-containing s

101 Six TPA parameters (hardness, adhesiveness, chewiness, springiness, cohesiveness, and

102 solvent-free nature enables their negligible adhesiveness compared to commercially available silicone

103 The observed increased cellular adhesiveness correlated with MP-induced upregulation of

104 e citrate-mediated crosslinking, whereas its adhesiveness decreased.

105 positively and negatively regulate cadherin adhesiveness depending on signals that so far remain uni

106 anes supporting previous evidence that hyper-adhesiveness depends on the organised arrangement of des

107 activity and a mediator of endothelial cell adhesiveness described here, NRP-1 emerges as a promisin

108 macrophages is accompanied by increased cell adhesiveness, due in part to the activation of alpha4bet

109 al signaling responses to SDF-1, but reduced adhesiveness, F-actin assembly, and reduced motility.

110 ibly requires dynamic regulation of integrin adhesiveness for endothelial and extracellular matrix li

111 ellular adaptors but do not predict cellular adhesiveness for immobilized ligand.

112 cytoplasmic domain mutants that alter LFA-1 adhesiveness for intercellular adhesion molecule-1.

113 xin-activation of HIECs resulted in enhanced adhesiveness for leukocytes.

114 arginine or shear stress reduces endothelial adhesiveness for monocytes and inhibits atherogenesis.

115 l feeding of rabbits induces enhanced aortic adhesiveness for monocytes and WEHI78/24 monocytoid cell

116 nt-sensitive signaling mediating endothelial adhesiveness for monocytes.

117 activity, VCAM-1 expression, and endothelial adhesiveness for monocytes.

118 Although HUVEC exhibited maximal adhesiveness for platelets after 2 to 4 hours, complete

119 On short time scales, adhesiveness for platelets is activated by elongation of

120 Both LTC4 and LTD4 enhanced endothelial adhesiveness for PMN, in part, by stimulating mobilizati

121 CAM-1 surface expression and mRNA as well as adhesiveness for T cells.

122 with HUVECs, unstimulated HIMECs showed less adhesiveness for U937 and MOLT4 cells and neutrophils, b

123 Hardness, adhesiveness, gumminess and chewiness levels decreased s

124 How the overall adhesiveness (i.e. the avidity) of receptor/ligand inter

125 vide direct support for the concept of hyper-adhesiveness in desmosomes.

126 hip exists between retrograde actin flow and adhesiveness in moving keratocytes.

127 g pathways leading to the change of integrin adhesiveness in neutrophils, monocytes, and lymphocytes.

128 olume at 65 degrees C, and high hardness and adhesiveness; in contrast, the low-AM starch of Tainung

129 hibitory responses, acquisition of increased adhesiveness, increased local immunosuppression, and enh

130 ed the role of mu-calpain in the endothelial adhesiveness induced by Ang II.

131 Reduced adhesiveness induced through the Eph/R-Ras pathway may e

132 either intracellular activation of integrin adhesiveness (inside-out signaling) or ligand binding (o

133 Platelet adhesiveness is critically dependent on agonist-induced

134 o resist premature bond disruption, selectin adhesiveness is enhanced by tensile forces that promote

135 onclude that the physiological role of sperm adhesiveness is in the mechanism of restricted sperm ent

136 bout how the appropriate balance of integrin adhesiveness is maintained in order to optimize the migr

137 to our growing understanding of how integrin adhesiveness is regulated and raise the notion of the ex

138 Dynamic regulation of integrin adhesiveness is required for immune cell-cell interactio

139 suggesting that heterogeneity of endothelial adhesiveness is responsible for velocity variation.

140 population is already endowed with a minimum adhesiveness level.

141 s well as biochemical modifications to their adhesiveness may alter the overall permeability of the c

142 eading to cell stiffening and an increase in adhesiveness mediated through alterations in beta2 integ

143 of genes predicted to increase cell surface adhesiveness, mediated by changes in bacterial signallin

144 hanges including alterations in cell growth, adhesiveness, motility, morphology, and organization of

145 Because of the increased Mac-1 adhesiveness, neutrophil crawling was impaired in CD45E6

146 rty but instead arises from a combination of adhesiveness, nuclear volume, contractility, and cell st

147 Here, we assayed the toxicity and adhesiveness of 90 MRSA (methicillin resistant S. aureus

148 CHO cells conferred hyaluronidase-sensitive adhesiveness of a mucosal T cell line via the lymphocyte

149 s observation that cytohesin-1 regulates the adhesiveness of alphaLbeta2 integrins at the plasma memb

150 egulation indicates that the diminished cell adhesiveness of CD82-expressing Du145 cells on laminin l

151 The adhesiveness of CHO cells expressing both full-length Po

152 Earlier studies have shown that the adhesiveness of cultured DMEC. from normal skin for lymp

153 nd 2.5-fold at 4 weeks, P<0.001) and induced adhesiveness of cultured human EPCs by upregulation of t

154 py revealed increased softness and decreased adhesiveness of EGF-stimulated cancer cells, implicating

155 of endothelial cells with ADMA increased the adhesiveness of endothelial cells for THP-1 cells in a c

156 or COX inhibitor) inhibited Erk activity and adhesiveness of formylmethionyl-leucyl-phenylalanine- an

157 or (TNF)-alpha expression, which may enhance adhesiveness of gastric capillaries for neutrophils by a

158 The adhesiveness of HEV ligands for L-selectin and alpha4bet

159 form in membrane microvesicles, and induces adhesiveness of human endothelial cells for neutrophils.

160 kinase Erk in CD11b/CD18 integrin-dependent adhesiveness of human neutrophils, a critical step in in

161 The adhesiveness of integrin alpha(L)beta(2) is modulated by

162 The adhesiveness of integrins is regulated through a process

163 been demonstrated previously to modulate the adhesiveness of LFA-1.

164 Lymphocyte activation triggers adhesiveness of lymphocyte function-associated antigen-1

165 tants stimulated a prolonged increase in the adhesiveness of Mac-1 (alpha M beta 2, CD11b/CD18) for i

166 The persistent adhesiveness of matrices formed from fibrinogen derivati

167 The adhesiveness of microspheres depends on the strength of

168 Zeb1 represses cdh1 expression to fine-tune adhesiveness of migrating deep blastodermal cells.

169 family (ADAMTS-13), that functions to reduce adhesiveness of newly released, unusually large (UL), hy

170 In order to test the adhesiveness of PLP-null compact myelin lamellae we soak

171 Mechanisms by which impaired adhesiveness of PLP-null myelin lamellae and fluctuation

172 cal type I pilus significantly increases the adhesiveness of poorly adhering highly capsulated strain

173 not p38 activation, abolished the increased adhesiveness of PP2Ac (alpha)-depleted 293 cells to fibr

174 -regulated kinase (ERK1/2) and the increased adhesiveness of PP2Acalpha-depleted 293 alpha(IIb)beta(3

175 associated protein (IAP; CD47) increases the adhesiveness of sickle RBCs (SS RBCs) by activating sign

176 recruitment by acting as a regulator of the adhesiveness of the b2-integrin lymphocyte function-asso

177 udy, the effect of a polysaccharide panel on adhesiveness of the CD-associated AIEC strain LF82 was a

178 r remodeling of the cytoskeleton, change the adhesiveness of the cell to the matrix, and activate mot

179 gative R-ras into adherent cells reduced the adhesiveness of the cells, indicating that endogenous R-

180 of Po have a dominant-negative effect on the adhesiveness of the full-length Po.

181 of LDLR-deficient mice, and the increase in adhesiveness of the vessels was P-selectin-dependent.

182 Adhesiveness of VLA-4 (alpha 4 beta 1, CD29/CD49d) for v

183 lls is likely responsible for the diminished adhesiveness on laminin and, subsequently, results in th

184 ate along gradients of chemical cues, matrix adhesiveness, or matrix stiffness.

185 monocytes from mice on a WD increased their adhesiveness over 5 wk, rising to twice that of mice on

186 vading front is influenced by changes in the adhesiveness parameters, and detail how the invasiveness

187 In addition to increased adhesiveness, PIPKIgamma90-deficient T cells exhibit inc

188 aberrantly expressed Muc4 can influence the adhesiveness, proliferation, viability and invasiveness

189 naling, integrin activation, and cell-matrix adhesiveness required for tumor progression.

190 IP-9-increased motility and -decreased adhesiveness required the intracellular protease calpain

191 of hMSC HCELL with E-selectin triggers VLA-4 adhesiveness, resulting in shear-resistant adhesion to l

192 signals resulting in activation of integrin adhesiveness (Step 2), with ensuing firm adherence on th

193 uanosine triphosphatase Rap1 regulates LFA-1 adhesiveness through one of its effectors, Rap1-interact

194 migration was associated with increased cell adhesiveness to collagen and laminin and enhanced expres

195 mediated endothelial selectin expression and adhesiveness to effector T cells.

196 n of aortic smooth muscle cells and monocyte adhesiveness to extracellular matrix.

197 3 treatment induces increased mesangial cell adhesiveness to fibronectin.

198 als resulted in decreased Rap1-GTP and LFA-1 adhesiveness to ICAM-1, thus impairing T-cell chemotaxis

199 sion molecule-1 (VCAM-1) and increased their adhesiveness to inflamed or atherosclerotic endothelium.

200 th abrupt elongation, thereby increasing its adhesiveness to platelets and collagen.

201 the structure and rheology of vWF A1 domain adhesiveness to the platelet GPIbalpha receptor.

202 d MCP-1 increase vascular smooth muscle cell adhesiveness to type III collagen.

203 n in Matrigel-coated filters, and heightened adhesiveness to type IV collagen substrata.

204 and that this correlates with differences in adhesiveness to type-I or type-III collagens.

205 The considered adhesiveness trait is costly, continuous and affects bot

206 r band 3 in at least one type of sickle cell adhesiveness via the exposure of normally cryptic membra

207 ate (cAMP) in the regulation of human SS RBC adhesiveness via the laminin receptor, basal cell adhesi

208 Adhesiveness was augmented if RF and UVA also were appli

209 This increased adhesiveness was completely eliminated by lisofylline in

210 d that in CD45E613R mutant neutrophils LFA-1 adhesiveness was impaired, and avidity was enhanced, whe

211 red, and avidity was enhanced, whereas Mac-1 adhesiveness was increased.

212 In addition, white cell adhesiveness was measured to assess the effects of lisof

213 Platelet adhesiveness was not affected by lisofylline.

214 Increased adhesiveness was not associated with an abnormal express

215 ines, while in lines over-expressing wt-APP, adhesiveness was slightly increased.

216 l rate, white blood cell count, and platelet adhesiveness were determined.

217 Surfactant reduces sputum adhesiveness, which contributes to difficulty in clearin

218 we find it necessary to downregulate cell-BM adhesiveness, which is consistent with experimental obse

219 ncrease in focal adhesions and enhanced cell adhesiveness, which may participate in the impaired rest

220 lucan gel showed a reduction in hardness and adhesiveness, which was confirmed by its rheological beh