ライフサイエンスコーパス: capillary tube

1 m the cytosol during vigorous suction into a capillary tube.

2 were obtained using a calibrated glass micro capillary tube.

3 inferior tear meniscus was depleted using a capillary tube.

4 ed between a plate-based system and a single capillary tube.

5 gmented by an immiscible oil and stored in a capillary tube.

6 ells undergo branching morphogenesis to form capillary tubes.

7 based on bead-packed columns, membranes, and capillary tubes.

8 rtic endothelial cells cultured within glass capillary tubes.

9 reating the channels as parallel cylindrical capillary tubes.

10 gration of EC and the formation of primitive capillary tubes.

11 e swimming of bacteria in micro channels and capillary tubes.

12 hrough the tongue in the same way as through capillary tubes.

13 solvent and transferred it to a needle via a capillary tubing.

14 deposited onto the surface of a piece of CE capillary tubing.

15 nanotubes (SWNTs) inside silica-lined steel capillary tubing.

16 urface of the inner wall of the fused silica capillary tubing.

17 We minimized solute dispersion by using capillary tubing (75 mum inside diameter, 70 cm long) fo

18 implest Criegee intermediate within a quartz capillary tube affixed to a pulsed valve to cool and iso

19 vasculature, primary endothelial cell-lined capillary tubes, although present, failed to connect int

20 ment was originally designed to be used with capillary tubes, an adapter that allows this instrument

21 The phone camera then photographs the capillary tube and analyzes the color components of the

22 Tears were collected by capillary tube and centrifuged.

23 the unique technology of small-volume glass capillary tubes and high-velocity air for the heating an

24 Endothelial monolayers were grown in capillary tubes and tested with and without interleukin-

25 t various time points via a microliter glass capillary tube, and the miniature sensors were then inse

26 ument, consisting of multiple rotary valves, capillary tubing, and miniaturized reaction vessels, for

27 mobile phone or a webcam as a detector, and capillary tube array configured with 36 capillary tubes

28 (2) an optical signal amplifier utilizing a capillary tube array.

29 nchrotron XRD method using a quartz/sapphire capillary tube as the synthesis reactor.

30 cells generated mature endothelial cells and capillary tubes as efficiently as mature mesenchymal cel

31 l tracking analysis, swarm plate assays, and capillary tube assays) showed that the cheA(2) mutant fa

32 tin and microtubule cytoskeletons to promote capillary tube assembly.

33 Furthermore, swarm plate and capillary tube chemotaxis assays demonstrated that cheX

34 Capillary tube chemotaxis assays indicated that only tho

35 A capillary tube coated with palladium is added between th

36 tic enzymes in the OMV did not contribute to capillary tube disruption, since blocking enzyme activit

37 and capillary tube array configured with 36 capillary tubes for signal enhancement.

38 This paper demonstrates nanostructured capillary tubes for surface enhanced Raman spectroscopy

39 t application of self-assembled CNTs in long capillary tubes for the development of gas chromatograph

40 that differentially control the processes of capillary tube formation (morphogenesis) versus capillar

41 ecause ectopic expression of miR-27a blocked capillary tube formation and angiogenesis.

42 s required for VEGFR-2-dependent endothelial capillary tube formation and proliferation.

43 nd pericyte-derived TIMP-3 to block both the capillary tube formation and regression pathways.

44 n lung microvascular endothelial cells using capillary tube formation and thymidine incorporation.

45 stochemistry, corneal neovascularization and capillary tube formation assay, and Western blot, respec

46 Both RPTEC and GEC induced VEGF-dependent capillary tube formation by co-cultured endothelial cell

47 OMV suppressed the capillary tube formation by cultured HUVEC.

48 and adhesion, migration, proliferation, and capillary tube formation by human endothelial cells.

49 Capillary tube formation by HUVEC cultured on an ECM was

50 d astrocytes, and dose-dependently increased capillary tube formation compared with nontreatment cont

51 genic growth factors, and signals regulating capillary tube formation during angiogenesis.

52 tion pathway that regulates endothelial cell capillary tube formation during angiogenesis.

53 tion of SMC proliferation, and inhibition of capillary tube formation in collagen gels.

54 inhibit angiogenesis in an in vitro model of capillary tube formation in fibrin gels.

55 ion, factor XIIIa inhibited endothelial cell capillary tube formation in fibrin in a dose-dependent m

56 s adhesion of endothelial cells and inhibits capillary tube formation in fibrin.

57 Angiogenesis was assessed by studying capillary tube formation in human microvascular endothel

58 tential of ECs by promoting EC migration and capillary tube formation in Matrigel plugs.

59 EC proliferation, migration, and capillary tube formation in vitro were suppressed more b

60 dothelial cells showed that IGPR-1 regulates capillary tube formation in vitro, and B16F melanoma cel

61 of hematopoietic cells as well as enhancing capillary tube formation in vitro.

62 t, and angiogenesis as measured by increased capillary tube formation in vitro.

63 ion in nude mice, in vitro three-dimensional capillary tube formation involving HUVEC and/or HTR8 tro

64 XIIIa produced a dose-dependent reduction in capillary tube formation of 60% to 100% in gammaA/gammaA

65 cell proliferation, migration, invasion, and capillary tube formation of cultured human umbilical vei

66 nhibited the differentiation, migration, and capillary tube formation of human umbilical vein endothe

67 cts chemotaxis and morphology and stimulates capillary tube formation of HUV-EC-C in vitro and angiog

68 wo antagonists (Y1+Y2, Y1+Y5, or Y2+Y5), and capillary tube formation on Matrigel was blocked by all

69 concentration-dependent strong inhibition of capillary tube formation on matrigel, retraction and dis

70 ed in a three-dimensional coculture model of capillary tube formation on Matrigel.

71 Its upregulation parallels the NPY-induced capillary tube formation on reconstituted basement membr

72 le inhibiting endothelial cell migration and capillary tube formation predominantly through disruptio

73 of fibrin with endothelial cells stimulates capillary tube formation thus promoting angiogenesis.

74 al vein endothelial cells (HUVEC) can induce capillary tube formation via the interaction of fibrin b

75 ures were applied with endothelial cells and capillary tube formation was compared under the above co

76 In vitro capillary tube formation was inhibited by chNKG2D T cell

77 o inhibited VEGF(165) induced proliferation, capillary tube formation, activation of VEGFR2 and MMP2

78 AGGF1-mediated EC proliferation, migration, capillary tube formation, and aortic ring-based angiogen

79 2ED promoted membrane protrusion, migration, capillary tube formation, and cell-cell interactions.

80 ited VEGF-mediated receptor phosphorylation, capillary tube formation, and proliferation of endotheli

81 (IPDX) on AdoR-mediated HREC proliferation, capillary tube formation, and signal-transduction pathwa

82 LCS on HMVEC-dNeo proliferation, migration, capillary tube formation, gene expression, and productio

83 on, yet inhibits cell migration and in vitro capillary tube formation, whereas co-knockdown of PML co

84 down-regulated alpha(v)beta(3) and inhibited capillary tube formation, with the extent of down-regula

85 in-1 promoter and modulates endothelial cell capillary tube formation.

86 ell proliferation and migration, and induced capillary tube formation.

87 ion, cell cycle protein phosphorylation, and capillary tube formation.

88 in an integrin-dependent manner and inhibits capillary tube formation.

89 eration, ERK activation, cell migration, and capillary tube formation.

90 ntial step of angiogenesis in fibrin, namely capillary tube formation.

91 the extracellular matrix (ECM) to facilitate capillary tube formation.

92 table analog of cGMP, 8-bromo-cGMP, restored capillary tube formation.

93 ions including proliferation, migration, and capillary tube formation.

94 ration, invasion, adhesion, and VEGF-induced capillary tube formation.

95 ells showed that SPIN90/WISH is required for capillary tube formation.

96 h affinity and also induced endothelial cell capillary tube formation.

97 ll processes of adhesion, proliferation, and capillary tube formation.

98 in increased EC proliferation, motility, and capillary tube formation.

99 se-dependent increases in cell migration and capillary tube formation.

100 on of NOS partially decreased Niacin-induced capillary tube formation.

101 y and significantly decreased Niacin-induced capillary tube formation.

102 e-induced endothelial cell proliferation and capillary tube formation.

103 ignificantly lost their capacity to suppress capillary tube formation.

104 inhibitors did not reduce the suppression of capillary tube formation.

105 ring explant cultures and in vitro on HUVEC capillary-tube formation on Matrigel at low nanomolar co

106 Furthermore, light-dye treatment increased capillary tube hematocrit by 60% in 40-microns-long capi

107 plicated in the regulation and modulation of capillary tube hematocrit, permeability, and hemostasis.

108 pe pericytes and were less able to stabilize capillary tubes in three-dimensional culture and less ab

109 sEng inhibits formation of capillary tubes in vitro and induces vascular permeabili

110 ciently infected human endothelial cells and capillary tubes in vitro.

111 mum diameter leak holes represented by glass capillary tubes, in recirculating solutions that are sup

112 ded solvent flow rate, temperature of heated capillary tube, incident and reflection angle, sheath ga

113 The capillary tube integrates the SERS sensor and the nanofl

114 ected the syringe within the pump to a glass capillary tube (internal diameter, 0.579 mm) shallowly e

115 Inside the capillary tube, inverse opal photonic crystal (IO PhC) w

116 a dominant negative form of EphA2 inhibited capillary tube-like formation by human umbilical vein en

117 culture plates inhibited 12(R)-HETrE-induced capillary tube-like formation, suggesting that VEGF medi

118 al microvascular endothelial cells to form a capillary tube-like structure on Matrigel.

119 d cell motility and reduced the formation of capillary tube-like structures in vitro.

120 ion of neutrophils from a cell pellet in the capillary tube migration assay.

121 he chemotherapeutic agent vinblastine, rapid capillary tube network collapse occurred followed by end

122 es, kidney pericytes bound to and stabilized capillary tube networks in three-dimensional gels and in

123 mined by their capacity to form a network of capillary tubes on an extracellular matrix (ECM).

124 roL or less) is first collected into a clear capillary tube or microtube, which is then inserted into

125 roL or less) is first collected into a clear capillary tube or microtube, which is then inserted into

126 the process of differentiation and in vitro capillary tube organization of RFCs.

127 8 induced endothelial cell proliferation and capillary tube organization while neutralization of IL-8

128 of IL-8 by anti-IL-8 Ab blocks IL-8-mediated capillary tube organization.

129 oring is demonstrated in 184-microm diameter capillary tubing over a range of 2-25 cm/s (500 nL/s to

130 injection of a solution at 4 bar pCO2 into a capillary tube packed with crushed calcite.

131 lute H2SO4 is formed on the top of two metal capillary tubes placed in a concentric annular arrangeme

132 The capillary tube provides the reference peak for quantific

133 Continuous-flow, microfluidic reactions in capillary tube reactors are described, which are capable

134 MP-2 and pericyte TIMP-3 expression leads to capillary tube regression in these cocultures in a matri

135 illary tube formation (morphogenesis) versus capillary tube regression in three-dimensional (3D) coll

136 folding of PI3K and Akt to alter endothelial capillary tube stability in vitro.

137 derived TIMP-3 are shown to coregulate human capillary tube stabilization following EC-pericyte inter

138 In vitro secretoneurin induced capillary tubes, stimulated proliferation, inhibited apo

139 iter and smaller liquid volumes inside glass capillary tubes that have an optically transparent thin

140 l migration by 42% and promoted formation of capillary tubes; these effects were blocked by a neutral

141 difference in pressure between two ends of a capillary tube through which the solution is flowing at

142 Endothelial cells form capillary tubes through the process of intracellular tub

143 (aminoalkyl)silane-derivatized fused-silica capillary tube via a biotin/streptavidin/biotin linkage.

144 osited on the outside of glass melting point capillary tubes were analyzed in positive ion mode with

145 ween circulating cells and P-selectin-coated capillary tubes were measured.

146 es of capillary loops together into a single capillary tube where capillary isoelectric focusing (CIE

147 microsprayer, but with an extended sampling capillary tube which can reach into the depths of 96-, 3

148 x 127 microm inner diameter stainless steel capillary tube which was used to introduce gas into the

149 oscopy with standard instrumentation using a capillary tube with a secondary standard.

150 Fused-silica capillary tubes with 50-microm bores have been chemicall

151 croL serum pushed directly from self-sealing capillary tubes with a dispenser).

152 tion of a complex interconnecting network of capillary tubes with readily identifiable lumens.

153 roach for microarrays that uses fused-silica capillary tubes with tapered tips for printing pins and

154 was loaded into 150-micron-i.d. fused-silica capillary tubing with a pulled 5-10-micron needle tip at

155 minute-range flow through a 0.5-mm-diameter capillary tubing with as low as 250 mV of applied voltag

156 nt consumed by the conventional WB using the capillary tube without any need of special micromachinin