ライフサイエンスコーパス: adhesive property

1 -standing film (nanosheet) that has a highly adhesive property.

2 through enhancing mutant Htt aggregation and adhesive property.

3 g of catechol and subsequently decreased its adhesive property.

4 ar portions serving the universal and robust adhesive properties.

5 ng signaling pathways or modulating cellular adhesive properties.

6 osylation of MSP1a significantly reduced its adhesive properties.

7 of viscoelastic gels and in many cases have adhesive properties.

8 ies, and the other (integrins) with strongly adhesive properties.

9 y each receptor that underpin their specific adhesive properties.

10 d a distinct class of membrane proteins with adhesive properties.

11 ar stress to promote significant and tunable adhesive properties.

12 ovary (CHO) cells and examined the relative adhesive properties.

13 first direct evidence that fertilin beta has adhesive properties.

14 imers and strand-swap dimers, with different adhesive properties.

15 lysis confirm that TCPs are enriched for bio adhesive properties.

16 ce that could have been recognized as having adhesive properties.

17 e adhesive without altering the physical and adhesive properties.

18 ested to be highly regulated so as to change adhesive properties.

19 rt artificial adhesive surfaces with tunable adhesive properties.

20 y enhanced tensile properties, toughness and adhesive properties.

21 g installed in the polycarbonate domains for adhesive properties.

22 n to a substrate or fine-tune the glycocalyx adhesive properties.

23 providing two cadherin pools with different adhesive properties.

24 rior to all other substances in terms of its adhesive properties.

25 eatures typically exhibit intriguing surface adhesive properties.

26 ) were isolated based on their intercellular adhesive properties.

27 rticles will exhibit interesting anisotropic adhesive properties.

28 e notion that myelin TJs exhibit significant adhesive properties.

29 d choline-binding protein displaying various adhesive properties.

30 d simultaneously mapped their mechanical and adhesive properties.

31 offer independent control over physical and adhesive properties.

32 lgi apparatus, respectively, activates their adhesive properties.

33 aminin in vitro, suggesting that MTP possess adhesive properties.

34 asion and metastasis by reducing cancer cell adhesive properties.

35 These cell clusters also have differential adhesive properties: adherens junction components are up

36 roughout the genome, decreased activation of adhesive properties and cell adhesion genes, and a decre

37 further demonstrate that regulation of cell adhesive properties and cell morphology may underlie the

38 Yersinia pestis the autotransporter YapE has adhesive properties and contributes to disease in the mo

39 odify axon behavior in vitro by altering the adhesive properties and cytoskeleton of olfactory recept

40 data show that ZIKV manipulates the monocyte adhesive properties and enhances monocyte transmigration

41 rformance dental composites, offering strong adhesive properties and improved mechanical strength.

42 Amniotic membrane has anti-adhesive properties and is felt to promote epithelializa

43 roduct(s) of fibrinogen cleavage have strong adhesive properties and may be similar to fibrin.

44 ydrogels were optimized first regarding cell adhesive properties and mechanical properties to best su

45 n biofouling communities due to their strong adhesive properties and quick settlement times.

46 Moreover this action is dependent on the adhesive properties and the C terminus of Cx43 but not t

47 of developing DRG neurons may modulate their adhesive properties and thereby support axonal developme

48 due to their low mechanical stability, poor adhesive property and contamination risk.

49 results in substantial enhancement of OPN's adhesive properties, and because VPF/VEGF promotes incre

50 These processes determine the shape, adhesive properties, and movement of cells, and the Rho

51 n a microchannel hosting a constriction with adhesive properties, and report evidence of a striking v

52 (selectins or selectin ligands) with weakly adhesive properties, and the other (integrins) with stro

53 role in hemostasis and thrombosis, platelet adhesive properties are central to a variety of pathophy

54 The mechanisms governing these competing adhesive properties are not fully understood.

55 State-of-the-art models to describe adhesive properties are unable to explain these experime

56 ng on resin physicochemical, mechanical, and adhesive properties, as well as the antimicrobial respon

57 It also allows for the variation of these adhesive properties, as would occur in the presence of a

58 that can be used repeatedly with peeling and adhesive properties better than the natural gecko foot.

59 nal consequences of mismatched stiffness and adhesive properties between neighboring normal cells on

60 ntified the impact of polysialylation on the adhesive properties both of membrane-bound neural cell a

61 ro active agent release profile and in vitro adhesive properties, both to oral mucosa and to teeth su

62 ells not only positively influenced cellular adhesive properties but also reversed the transformed ph

63 Robust binding was independent of pilus-1 adhesive properties but required Fab-dependent recogniti

64 on complex and the consequent acquisition of adhesive properties by the cells.

65 The gelation dynamics and adhesive properties can be systematically tuned by varyi

66 YapE also demonstrates adhesive properties capable of mediating interactions wi

67 entify key developmental mechanisms, such as adhesive properties, cell densities and migration of cor

68 nTAl was found to have superior physical and adhesive properties compared to existing oral technologi

69 adable backbones and enhanced mechanical and adhesive properties could be readily generated from this

70 llular interactions by inducing repulsive or adhesive properties, depending on forward or reverse sig

71 Regulation of the adhesive properties during erythroid differentiation may

72 ntion in dentistry due to its structural and adhesive properties, enhancing the mechanical performanc

73 ed enzyme, the recombinant proteins retained adhesive properties equal to the natural T. vaginalis AP

74 racteristics, e.g. their density, fragility, adhesive properties, etc.

75 receptor complexes rapidly alters the cell's adhesive properties facilitating high avidity cell-ligan

76 Furthermore, adhesive properties for materials with chains of interme

77 's gliding speed and its ability to modulate adhesive properties for successful exit from the inocula

78 ster content of the multiblock copolymers on adhesive properties, has resulted in a modular hot-melt

79 Hydrogels with adhesive properties have potential for numerous biomedic

80 ytohesin 1 (CYTH1) as a critical mediator of adhesive properties in primary human cord blood-derived

81 from vitelline membrane, and that this anti-adhesive property is important to prevent precocious adh

82 antigen I/II family polypeptide that confers adhesive properties linked to pathogenesis in GBS.

83 Moreover, the adhesive property occurred in both homotypic with Cx50 e

84 Mimicking the non-adhesive properties of a glycocalyx provides a potential

85 ulation modulates alpha IIb beta 3-dependent adhesive properties of a human erythroleukemic (HEL) cel

86 ereby thrombin cleavage of HC1 regulates the adhesive properties of an inflammatory HA matrix.

87 Thus, tRA alters the adhesive properties of APL cells by inducing the express

88 between tRA-induced differentiation and the adhesive properties of APL cells.

89 , produced by Bacillus thuringiensis, on the adhesive properties of BBMVs were investigated.

90 2 enhanced the chemotaxis, chemoinvasion and adhesive properties of breast cancer cells; parameters t

91 The mechanical and adhesive properties of cancer cells significantly change

92 Due to the supposed cell adhesive properties of CD31, specific monoclonal antibod

93 ort-term reaggregation assays to compare the adhesive properties of cells derived from midbrain and a

94 Adhesive properties of cells undergoing morphogenetic re

95 pe I transmembrane mucin that can affect the adhesive properties of cells, contains a large extracell

96 sting one function of Dll here is to control adhesive properties of cells.

97 Here, we achieved tunable adhesive properties of chemically recyclable polyolefin-

98 residue known for its essential role in the adhesive properties of classic cadherins.

99 We also compared the hydrophobic and adhesive properties of DeltabclA and wild-type spores.

100 In contrast, TGF-beta1 has no effect on the adhesive properties of DMEC from psoriatic plaques, and

101 udy of the substrate and oxidation-dependent adhesive properties of dopa.

102 has previously been used to demonstrate the adhesive properties of E-cadherin.

103 ortant differences regarding the nonspecific adhesive properties of each layer.

104 ating the proper migration and/or changes in adhesive properties of early embryonic cells.

105 The intrinsic contractile, migratory, and adhesive properties of endothelial cells are central det

106 important role in mediating the cell-matrix adhesive properties of epithelial cells.

107 hanism whereby circulating fibrinogen alters adhesive properties of fibrin clots may have important i

108 f the multilayer formation, the physical and adhesive properties of fibrinogen matrices prepared from

109 he full dissolution of the networks, loss of adhesive properties of films (decreases in the measured

110 To examine the adhesive properties of full-length PECAM-1 in a native l

111 To obtain information on the adhesive properties of GalCer bilayers, we incorporated

112 migration, raising the possibility that the adhesive properties of gap junctions may have an importa

113 Waals mechanism implies that the remarkable adhesive properties of gecko setae are merely a result o

114 In this study, we set out to investigate the adhesive properties of H7 and H6 flagella.

115 apid, temporally progressive decrease in the adhesive properties of hepatocytes exposed to such serum

116 ally, we found that purified Fpn altered the adhesive properties of HT29 intestinal epithelial cells.

117 may play a functional role in enhancing the adhesive properties of human erythrocytes by engaging ba

118 mains which might contribute to the specific adhesive properties of IEs.

119 SFA measurements and are used to extract the adhesive properties of individual amino acids within the

120 Here we have studied the adhesive properties of integrin alphaLbeta2 containing m

121 may modulate the molecular interactions and adhesive properties of its ectodomain.

122 ity of the molecule and demonstrate that the adhesive properties of McaP do not require its lipolytic

123 stages of erythroid differentiation, but the adhesive properties of more primitive murine erythroid p

124 tly with glycosaminoglycans, we examined the adhesive properties of multiple monovalent and multivale

125 ocess, draws inspiration from the remarkable adhesive properties of mussel-inspired molecules.

126 acquisition of thioflavin S(+), amyloid-like adhesive properties of mutant Htt aggregates and a conco

127 The adhesive properties of Mytilus edulis foot proteins mfp-

128 nisms for this trait may perhaps be the anti-adhesive properties of NDM or its potential effect on in

129 s may be caused by abnormalities in the cell adhesive properties of neuroepithelial cells and suggest

130 el Toro et al. (2017) show that changing the adhesive properties of neurons in the normally lissencep

131 The growth-inhibitory and anti-adhesive properties of NG2 may limit the lateral extensi

132 the hindbrain, this is a result of different adhesive properties of odd- and even-numbered segments (

133 BC) to C. albicans adhesion and assessed the adhesive properties of other NT-Als3 features in the abs

134 hod is capable of dramatically improving the adhesive properties of PE surfaces.

135 The finding that the adhesive properties of PECAM-1 are regulatable suggests

136 pxB leads to down-regulation of the multiple adhesive properties of pneumococcus which, in turn, may

137 effect of alpha-actinin-4 deficiency on the adhesive properties of podocytes in vivo and in a cell c

138 of Yersinia pestis consists of fimbriae with adhesive properties of potential importance for the path

139 is study examined the antibacterial and anti-adhesive properties of pure plant extracts (PPEs) of gre

140 Our findings suggest that the adhesive properties of recombinant Pvfp-5beta make it an

141 ocesses, such as immune response modulation, adhesive properties of selectins, and gastrointestinal t

142 f keratinocytes, and the preservation of the adhesive properties of stratified epithelium.

143 GF, produced by the ectoderm, influences the adhesive properties of the adjacent mesoderm cells durin

144 discoideum motility with an emphasis on the adhesive properties of the cell-substratum contact.

145 V-histidine kinase, LovK, that regulates the adhesive properties of the cell.

146 This lock may be achieved by a change in the adhesive properties of the cells: cadherin-based adhesio

147 sociated with reduced IL-1 receptor-mediated adhesive properties of the endothelium and is protective

148 determine the effect of Psgl-1 deficiency on adhesive properties of the endothelium and on leukocyte

149 cribe a systematic investigation of the cell-adhesive properties of the extracellular region of RPTPm

150 of the intracellular C terminus enhances the adhesive properties of the extracellular surface of AQP0

151 The mechanical and adhesive properties of the fuzzy coat are modulated by e

152 a or Cys435Ala substitution of GPIIIa on the adhesive properties of the GPIIb-IIIa complex.

153 ically, we address the impact of t-RA on the adhesive properties of the human mature B and T cell lin

154 To study the adhesive properties of the LFA-1 I domain, we stably exp

155 ecades, many scenarios based on the enhanced adhesive properties of the membrane of sickle red blood

156 initial mutation, and the proliferative and adhesive properties of the mutant cells, to obtain stati

157 This is likely due to abnormal adhesive properties of the mutant hepatocytes, which may

158 polysialic acid expression and influence the adhesive properties of the neural cell adhesion molecule

159 ss-linking may explain in part the increased adhesive properties of the Pro(33) variant of integrin b

160 zed the regulatory network of YloA-dependent adhesive properties of the probiotic B. subtilis natto (

161 ro and in vivo experiments indicate that the adhesive properties of the proteolipid protein, along wi

162 xpression, ordered spatial localization, and adhesive properties of the RGM-related family of membran

163 es stringent requirements for smoothness and adhesive properties of the surface, which most common su

164 quartz surfaces in an attempt to change the adhesive properties of the surfaces.

165 ephrin activation may in part be due to the adhesive properties of the tissue.

166 ibronectin type III domains that mediate the adhesive properties of this group of transmembrane prote

167 unique sulfated structures may modulate the adhesive properties of TN-R over the course of developme

168 rminal fragment can functionally restore the adhesive properties of Tractin.

169 llular activation signals that influence the adhesive properties of vascular cells that express this

170 required to maintain proper conformation and adhesive properties of VE-cadherin, do not influence the

171 subvirucidal concentrations, EB changes the adhesive properties of virions, causing aggregation at h

172 9.5 and is most likely a result of different adhesive properties of wild-type and mutant cells.

173 This role is mediated in part through the adhesive properties of Xcyr61 and its related ability to

174 ectrical field stimulation to deactivate the adhesive property of catechol-containing adhesive that i

175 Anti-adhesive property of extracts was evaluated in Caco-2 ce

176 In vitro, the anti-adhesive property of NDM was validated on epithelial cel

177 m by which Disabled-1 signaling controls the adhesive property of neurons to radial glia, thereby mai

178 developmentally regulated and modulates the adhesive property of the neural adhesion molecule, N-CAM

179 degradation of fibrin(ogen) and also confer adhesive properties on cells because Mac-1 and uPAR bind

180 que to determine the spatial distribution of adhesive properties on rolling cell surfaces.

181 Changes in adhesive properties on tumor endothelial subclones are a

182 onstrate that the H6 and H7 flagella possess adhesive properties, particularly the ability to bind mu

183 4beta1 and alpha5beta1 confer different cell adhesive properties, particularly with respect to focal

184 al responses of cells, such as stiffness and adhesive properties, play a significant role in their ph

185 elucidate protocadherin-15's structural and adhesive properties relevant in disease.

186 These are the smallest peptides with adhesive properties reported to date and show remarkable

187 At the leading edge, cells show altered adhesive properties such that they form ectopic contacts

188 Like YapV, YapK and YapJ demonstrated adhesive properties, suggesting that their previously re

189 ribute to regulating changes in cell surface adhesive properties that affect the propensity of cells

190 oordination of alterations in cell shape and adhesive properties that are mediated by cytoskeletal dy

191 is can provide T lymphocytes with motile and adhesive properties that are uniquely suited toward alte

192 glycoprotein displays both adhesive and anti-adhesive properties that contribute to the formation and

193 alized to the plasma membrane, Prmp displays adhesive properties that may be important for linking th

194 This gives rise to a spectrum of adhesive properties that strongly influences interaction

195 Tuning adhesive properties through in situ electrochemical oxid

196 om the binding of bacteria with well-defined adhesive properties to blots of SDS-PAGE-separated parot

197 reatment of cells with 5T-Fuc impaired their adhesive properties to immobilized adhesion molecules an

198 sed that inhibition of apoptosis and altered adhesive properties to the bone marrow microenvironment

199 in-transfected cell lines showed significant adhesive properties under conditions where cells transfe

200 c proteins, indicating that the amyloid-like adhesive property underlies the neurotoxicity of mutant

201 ce both Daudi and Jurkats do not alter their adhesive properties upon t-RA treatment.

202 in thrombus formation, we analyzed receptor adhesive properties using Chinese hamster ovary and huma

203 The link between the chemical and the adhesive properties was established by non-negative matr

204 ) and at comparable length scales, the local adhesive properties were examined using atomic force mic

205 The tensile, swelling, and adhesive properties were explored, finding that both at

206 As with HIV-infected EC, adhesive properties were linked to the capacity of Vpu t

207 the Vpu gene, CD40 upregulation and BL-cell adhesive properties were lost, indicating an essential r

208 eries of oligopeptides with beta-forming and adhesive properties, were synthesized and analyzed for a