ライフサイエンスコーパス: substrata

1 ional to the elastic modulus of the adhesive substrata.

2 nant and nonmalignant cells grown on plastic substrata.

3 s by passage in monolayer culture on plastic substrata.

4 heightened adhesiveness to type IV collagen substrata.

5 rsed as soon as the cells were detached from substrata.

6 able displacements of sufficiently compliant substrata.

7 elanoma cells before and after attachment to substrata.

8 nd prevented spreading of cells on noncoated substrata.

9 axon outgrowth on rigid, but not compliant, substrata.

10 ional simulations of cells migrating on flat substrata.

11 elasticity of the cells and their underlying substrata.

12 cultured ex vivo on two-dimensional plastic substrata.

13 ly-defined human-derived media additives and substrata.

14 lamellipodial protrusions on permissive ECM substrata.

15 omplex essential for adhesion of the cell to substrata.

16 ovary cells migrating on fibronectin-coated substrata.

17 f blood platelets and cells to extracellular substrata.

18 and proportionately distributed within five substrata.

19 RF rates while interacting with two distinct substrata.

20 cellular aggregates deposited on each of the substrata.

21 vealed enhanced proliferation on vitronectin substrata.

22 -embryonic retinal neurite outgrowth on LN-1 substrata.

23 ollagenous) and independent (noncollagenous) substrata.

24 hen the cells are cultured on gelatinous ECM substrata.

25 of vascular smooth muscle cells on gradient substrata (0-4 kPa/100 mum, with absolute moduli of 1-80

26 an either fibronectin (23% and 16%) or glass substrata (7% and 1%) at shear rates of 30 and 60 dyne/c

27 l region characterised by different geologic substrata, a key locality to test the influence of both

28 in mediating the initial binding of cells to substrata, a novel role for an unconventional myosin.

29 The wild fish from sites with anoxic substrata accumulate metals (including As and Se) from t

30 stoma cell movement in 3D matrices and on 2D substrata across a range of collagen densities with syst

31 not express p125(FAK) but upon adherence to substrata activate the highly related calcium-dependent

32 urons were cultured on control substrata and substrata adsorbed with full-length native MAG extracted

33 ophage cell adhesion to extracellular matrix substrata and anti-integrin antibodies.

34 were also cultured on 2-dimensional plastic substrata and collagen I hydrogels for analysis, and the

35 ed motility as a sheet in 2-dimensional (2D) substrata and individually in confined spaces and invasi

36 ved on several types of extracellular matrix substrata and leads to elevated stability of focal adhes

37 beta(3) mediated close contact to fibrinogen substrata and led to the formation of ringlike patterns

38 that are both the initial colonizers of hard substrata and of great economic importance, are almost u

39 d hillock formation by cells on serum-coated substrata and prevented spreading of cells on noncoated

40 oval cell adhesion to CTGF and fibronection substrata and promoting transforming growth factor (TGF)

41 Primary rat neurons were cultured on control substrata and substrata adsorbed with full-length native

42 ed on profibrotic conditions including stiff substrata and TGF-beta1, and analyzed in terms of morpho

43 tes the rate of neurite extension on diverse substrata and within the intact spinal cord.

44 tions produced by traction forces in elastic substrata, and interference reflection microscopy reveal

45 the adherence of B. burgdorferi to a decorin substrata, and they did not recognize decorin in an extr

46 ile the interactions of cells with polymeric substrata are widely studied, the influence of cell-cell

47 ars adhere firmly but temporarily to various substrata as a result of underwater efficient adhesive s

48 ed neuron cultures only traveled across CSPG substrata as fasciculated axon bundles.

49 l adhesion on different extracellular matrix substrata as well as changes in cell-cell adhesion and c

50 lts for the limiting case of migration on 2D substrata as well as with recent experiments in 3D natur

51 vis growth cones extending on permissive ECM substrata assemble adhesive point contacts containing en

52 eosomal fragmentation in response to loss of substrata attachment.

53 igosaccharides reduces neutrophil rolling on substrata bearing E-, L-, and P-selectins and neutrophil

54 hat are typically expanded in vitro on stiff substrata before reimplantation.

55 ) (electrotaxis) as they navigate non-planar substrata but the relative potencies of electrotaxis and

56 binding domain, clustered upon attachment to substrata coated with CEC1-5.

57 and-dependent fashion when cells attached to substrata coated with the adhesive ectodomain of Xenopus

58 with Xenopus C-cadherin mutant molecules and substrata coated with the purified ectodomain of C-cadhe

59 collapse occurs upon contact with repulsive substrata, collapse of the VD growth cones may result fr

60 eir gills whereas those from sites with oxic substrata concentrate these elements through their diet

61 tripe assays of alternating CSPG and control substrata confirmed the nonpermissive nature of CSPGs fo

62 markedly reduced when plated on collagenous substrata, despite normal attachment and spreading.

63 l and chemical composition of the underlying substrata elicit local Ca(2+) signals within growth cone

64 and minerals, usually considered as an inert substrata for microbial colonization.

65 n adaptation for adhesion to the most common substrata for mussels, i.e., calcareous materials.

66 l discs was incorporated into tissue culture substrata for the culture of the human neuronal cell lin

67 discoidin I or moving on discoidin I-coated substrata form fewer tandems, but the trailing cell stil

68 he ability to move over and colonize surface substrata has been linked to the formation of biofilms a

69 oped, but finding chemically defined, robust substrata has proven difficult.

70 s for cell migration on two-dimensional (2D) substrata have described how various molecular and cellu

71 cell cohesiveness in a series of copolymeric substrata having different levels of cell-substratum adh

72 and the interactions between them and their substrata help establish the early biofilm community.

73 s were plated onto serum-coated or noncoated substrata in serum-free medium.

74 examined by plating cells on collagen-coated substrata in the presence of the antibody.

75 uring development would not grow across CSPG substrata, in a concentration-dependent manner.

76 r advantage with CABG was also found in most substrata, including diabetes.

77 e of soluble pluripotency factors, compliant substrata inhibit the nuclear localization of YAP and pr

78 awling motion of Dictyostelium discoideum on substrata involves a number of coordinated events includ

79 In this report, we use hydrogel-based substrata matched to biological tissue stiffness to inve

80 Subconfluent cells on serum-coated substrata migrated together, forming aggregates, but cel

81 fficient differentiation of stem cells using substrata of biomatrix scaffolds, tissue-specific extrac

82 mals are unable to spread on or migrate into substrata of collagen IV and are deficient in spreading

83 ability to attach to and extend neurites on substrata of laminin-1 (LN-1) during late embryogenesis,

84 icant lead-ALS associations were observed in substrata of PINP and CTX levels.

85 These brain regions may represent the neural substrata of response inhibition independent of other co

86 odontitis, develops biofilm microcolonies on substrata of Streptococcus gordonii but not on Streptoco

87 eriodontitis, attaches and forms biofilms on substrata of Streptococcus gordonii.

88 onectin- (FN) and Arg-Gly-Asp (RGD)-modified substrata of varying surface density.

89 e plasma membrane in cells cultured on stiff substrata or in collagen-rich regions of human breast tu

90 Additionally, culture of cells on substrata presenting recombinant T-cadherin protein (ace

91 absence of neurogenic factors, the effective substrata produce neurons rapidly (2 wk) and more effici

92 cies strongly associated with carbonate-rich substrata; reef corals diversified dramatically; and the

93 ted collagen-I from each genotype as culture substrata, relative to r/r, we show that WT collagen-I p

94 , forming aggregates, but cells on noncoated substrata remained evenly dispersed.

95 achment of cells to a laminin or fibronectin substrata specifically modified the direction of gene ex

96 ts at deeper sites were replaced by unstable substrata such as fine sediments and rubble.

97 greater on plasma fibronectin than on other substrata such as laminin and merosin.

98 or byssus, opportunistically to a variety of substrata that are wet, saline, corroded, and/or fouled

99 where single or groups of cells are grown in substrata that have elements of basement membrane leadin

100 ugh neurites grew cathodally on both Plastek substrata, the frequency of anodal turning was greater o

101 tegrin-dependent motility on two-dimensional substrata to integrin-independent motion following entry

102 at can be harvested and deposited on various substrata to promote osteogenic differentiation.

103 y helps the zebra mussel to firmly attach to substrata underwater, thereby causing severe economic an

104 tile periphyton, leaves and natural benthic substrata using submerged electrified frames in three st

105 library" of structurally related copolymeric substrata varying in their adhesivity to cells and a lib

106 izing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices

107 n or arginine-glycine-aspartate (RGD)-coated substrata, was enhanced significantly in these matrix-ad

108 ism, supported by liver extracellular matrix substrata; we envision that it will be used in the futur

109 In addition, migration rates over these substrata were two-fold higher and the level of focal ad

110 e glycol) content of a series of copolymeric substrata, whereas cell-cell cohesiveness was varied thr

111 Falcon tissue culture plastic or on laminin substrata, which are negatively charged, but neurites gr

112 We used a new silicone polymer to fabricate substrata whose compliance can be adjusted precisely by

113 thelial monolayers onto polydimethylsiloxane substrata with a range of viscosities and elasticities.

114 newal, and differentiation were inhibited on substrata with moduli of approximately 10 Pa.

115 nic cells were controlled on microfabricated substrata with regiospecific chemistry by confining atta

116 are protective against EMT, whereas stiffer substrata, with compliances characteristic of breast tum

117 Soft substrata, with compliances comparable to that of normal

118 Growth was oriented randomly on all substrata without an electric field.