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1 m the cytosol during vigorous suction into a capillary tube.
2 ous phase containing the measuring ions in a capillary tube.
3 were obtained using a calibrated glass micro capillary tube.
4  inferior tear meniscus was depleted using a capillary tube.
5 ed between a plate-based system and a single capillary tube.
6 gmented by an immiscible oil and stored in a capillary tube.
7 ells undergo branching morphogenesis to form capillary tubes.
8 based on bead-packed columns, membranes, and capillary tubes.
9 rtic endothelial cells cultured within glass capillary tubes.
10 reating the channels as parallel cylindrical capillary tubes.
11 gration of EC and the formation of primitive capillary tubes.
12 t packed bed columns by a bundle of parallel capillary tubes.
13 e swimming of bacteria in micro channels and capillary tubes.
14 hrough the tongue in the same way as through capillary tubes.
15 solvent and transferred it to a needle via a capillary tubing.
16 n interfacing with ferrules and fused silica capillary tubing.
17  deposited onto the surface of a piece of CE capillary tubing.
18  nanotubes (SWNTs) inside silica-lined steel capillary tubing.
19 urface of the inner wall of the fused silica capillary tubing.
20      We minimized solute dispersion by using capillary tubing (75 mum inside diameter, 70 cm long) fo
21 implest Criegee intermediate within a quartz capillary tube affixed to a pulsed valve to cool and iso
22  vasculature, primary endothelial cell-lined capillary tubes, although present, failed to connect int
23 ment was originally designed to be used with capillary tubes, an adapter that allows this instrument
24        The phone camera then photographs the capillary tube and analyzes the color components of the
25                      Tears were collected by capillary tube and centrifuged.
26  the unique technology of small-volume glass capillary tubes and high-velocity air for the heating an
27         Endothelial monolayers were grown in capillary tubes and tested with and without interleukin-
28 t various time points via a microliter glass capillary tube, and the miniature sensors were then inse
29 ument, consisting of multiple rotary valves, capillary tubing, and miniaturized reaction vessels, for
30  mobile phone or a webcam as a detector, and capillary tube array configured with 36 capillary tubes
31  (2) an optical signal amplifier utilizing a capillary tube array.
32 nchrotron XRD method using a quartz/sapphire capillary tube as the synthesis reactor.
33 cells generated mature endothelial cells and capillary tubes as efficiently as mature mesenchymal cel
34 l tracking analysis, swarm plate assays, and capillary tube assays) showed that the cheA(2) mutant fa
35 tin and microtubule cytoskeletons to promote capillary tube assembly.
36  Raman instrument could be combined with the capillary-tube-based SERS analytical tool for diagnosis
37                 Furthermore, swarm plate and capillary tube chemotaxis assays demonstrated that cheX
38                                              Capillary tube chemotaxis assays indicated that only tho
39                                            A capillary tube coated with palladium is added between th
40                                            A capillary-tube-derived SERS platform offers ultrasensiti
41 tic enzymes in the OMV did not contribute to capillary tube disruption, since blocking enzyme activit
42  and capillary tube array configured with 36 capillary tubes for signal enhancement.
43       This paper demonstrates nanostructured capillary tubes for surface enhanced Raman spectroscopy
44 t application of self-assembled CNTs in long capillary tubes for the development of gas chromatograph
45 that differentially control the processes of capillary tube formation (morphogenesis) versus capillar
46 ecause ectopic expression of miR-27a blocked capillary tube formation and angiogenesis.
47 s required for VEGFR-2-dependent endothelial capillary tube formation and proliferation.
48 nd pericyte-derived TIMP-3 to block both the capillary tube formation and regression pathways.
49 n lung microvascular endothelial cells using capillary tube formation and thymidine incorporation.
50 stochemistry, corneal neovascularization and capillary tube formation assay, and Western blot, respec
51                                              Capillary tube formation assays with human umbilical vei
52    Both RPTEC and GEC induced VEGF-dependent capillary tube formation by co-cultured endothelial cell
53                           OMV suppressed the capillary tube formation by cultured HUVEC.
54  and adhesion, migration, proliferation, and capillary tube formation by human endothelial cells.
55                                              Capillary tube formation by HUVEC cultured on an ECM was
56 d astrocytes, and dose-dependently increased capillary tube formation compared with nontreatment cont
57 tion pathway that regulates endothelial cell capillary tube formation during angiogenesis.
58 genic growth factors, and signals regulating capillary tube formation during angiogenesis.
59 tion of SMC proliferation, and inhibition of capillary tube formation in collagen gels.
60 inhibit angiogenesis in an in vitro model of capillary tube formation in fibrin gels.
61 ion, factor XIIIa inhibited endothelial cell capillary tube formation in fibrin in a dose-dependent m
62 s adhesion of endothelial cells and inhibits capillary tube formation in fibrin.
63        Angiogenesis was assessed by studying capillary tube formation in human microvascular endothel
64  media that can regulate HUVEC migration and capillary tube formation in in vitro functional angiogen
65 tential of ECs by promoting EC migration and capillary tube formation in Matrigel plugs.
66             EC proliferation, migration, and capillary tube formation in vitro were suppressed more b
67 dothelial cells showed that IGPR-1 regulates capillary tube formation in vitro, and B16F melanoma cel
68  of hematopoietic cells as well as enhancing capillary tube formation in vitro.
69 t, and angiogenesis as measured by increased capillary tube formation in vitro.
70 ion in nude mice, in vitro three-dimensional capillary tube formation involving HUVEC and/or HTR8 tro
71 XIIIa produced a dose-dependent reduction in capillary tube formation of 60% to 100% in gammaA/gammaA
72 cell proliferation, migration, invasion, and capillary tube formation of cultured human umbilical vei
73 nhibited the differentiation, migration, and capillary tube formation of human umbilical vein endothe
74 cts chemotaxis and morphology and stimulates capillary tube formation of HUV-EC-C in vitro and angiog
75 wo antagonists (Y1+Y2, Y1+Y5, or Y2+Y5), and capillary tube formation on Matrigel was blocked by all
76 concentration-dependent strong inhibition of capillary tube formation on matrigel, retraction and dis
77 ed in a three-dimensional coculture model of capillary tube formation on Matrigel.
78   Its upregulation parallels the NPY-induced capillary tube formation on reconstituted basement membr
79 le inhibiting endothelial cell migration and capillary tube formation predominantly through disruptio
80  of fibrin with endothelial cells stimulates capillary tube formation thus promoting angiogenesis.
81 al vein endothelial cells (HUVEC) can induce capillary tube formation via the interaction of fibrin b
82 ures were applied with endothelial cells and capillary tube formation was compared under the above co
83                                     In vitro capillary tube formation was inhibited by chNKG2D T cell
84 o inhibited VEGF(165) induced proliferation, capillary tube formation, activation of VEGFR2 and MMP2
85  AGGF1-mediated EC proliferation, migration, capillary tube formation, and aortic ring-based angiogen
86 2ED promoted membrane protrusion, migration, capillary tube formation, and cell-cell interactions.
87 ited VEGF-mediated receptor phosphorylation, capillary tube formation, and proliferation of endotheli
88  (IPDX) on AdoR-mediated HREC proliferation, capillary tube formation, and signal-transduction pathwa
89  LCS on HMVEC-dNeo proliferation, migration, capillary tube formation, gene expression, and productio
90 on, yet inhibits cell migration and in vitro capillary tube formation, whereas co-knockdown of PML co
91 down-regulated alpha(v)beta(3) and inhibited capillary tube formation, with the extent of down-regula
92 h affinity and also induced endothelial cell capillary tube formation.
93 inhibitors did not reduce the suppression of capillary tube formation.
94 in-1 promoter and modulates endothelial cell capillary tube formation.
95 ell proliferation and migration, and induced capillary tube formation.
96 ion, cell cycle protein phosphorylation, and capillary tube formation.
97 in an integrin-dependent manner and inhibits capillary tube formation.
98 eration, ERK activation, cell migration, and capillary tube formation.
99 ntial step of angiogenesis in fibrin, namely capillary tube formation.
100 the extracellular matrix (ECM) to facilitate capillary tube formation.
101 table analog of cGMP, 8-bromo-cGMP, restored capillary tube formation.
102 inhibited cell proliferation, migration, and capillary tube formation.
103 ions including proliferation, migration, and capillary tube formation.
104 dothelial cell proliferation, migration, and capillary tube formation.
105 ells showed that SPIN90/WISH is required for capillary tube formation.
106 ll processes of adhesion, proliferation, and capillary tube formation.
107 in increased EC proliferation, motility, and capillary tube formation.
108 se-dependent increases in cell migration and capillary tube formation.
109 on of NOS partially decreased Niacin-induced capillary tube formation.
110 y and significantly decreased Niacin-induced capillary tube formation.
111 e-induced endothelial cell proliferation and capillary tube formation.
112 ration, invasion, adhesion, and VEGF-induced capillary tube formation.
113 ignificantly lost their capacity to suppress capillary tube formation.
114  ring explant cultures and in vitro on HUVEC capillary-tube formation on Matrigel at low nanomolar co
115   Furthermore, light-dye treatment increased capillary tube hematocrit by 60% in 40-microns-long capi
116 plicated in the regulation and modulation of capillary tube hematocrit, permeability, and hemostasis.
117 ricated by dip-coating a nonconductive glass capillary tube in a homogeneous PIM solution for three c
118 pe pericytes and were less able to stabilize capillary tubes in three-dimensional culture and less ab
119                   sEng inhibits formation of capillary tubes in vitro and induces vascular permeabili
120 ciently infected human endothelial cells and capillary tubes in vitro.
121 mum diameter leak holes represented by glass capillary tubes, in recirculating solutions that are sup
122 ded solvent flow rate, temperature of heated capillary tube, incident and reflection angle, sheath ga
123                                          The capillary tube integrates the SERS sensor and the nanofl
124 ected the syringe within the pump to a glass capillary tube (internal diameter, 0.579 mm) shallowly e
125                                   Inside the capillary tube, inverse opal photonic crystal (IO PhC) w
126 rs, embedded electrodes, and hydrogel-filled capillary tubing, is assembled modularly.
127  a dominant negative form of EphA2 inhibited capillary tube-like formation by human umbilical vein en
128 culture plates inhibited 12(R)-HETrE-induced capillary tube-like formation, suggesting that VEGF medi
129 al microvascular endothelial cells to form a capillary tube-like structure on Matrigel.
130 d cell motility and reduced the formation of capillary tube-like structures in vitro.
131  casting doubt on earlier observations using capillary tube maximum depth gauges(1), which may exagge
132 ion of neutrophils from a cell pellet in the capillary tube migration assay.
133 he chemotherapeutic agent vinblastine, rapid capillary tube network collapse occurred followed by end
134 es, kidney pericytes bound to and stabilized capillary tube networks in three-dimensional gels and in
135 necessary step to initiate and form branched capillary tube networks.
136  required for the assembly of human EC-lined capillary tube networks.
137 mined by their capacity to form a network of capillary tubes on an extracellular matrix (ECM).
138 roL or less) is first collected into a clear capillary tube or microtube, which is then inserted into
139 roL or less) is first collected into a clear capillary tube or microtube, which is then inserted into
140  the process of differentiation and in vitro capillary tube organization of RFCs.
141 8 induced endothelial cell proliferation and capillary tube organization while neutralization of IL-8
142 of IL-8 by anti-IL-8 Ab blocks IL-8-mediated capillary tube organization.
143 oring is demonstrated in 184-microm diameter capillary tubing over a range of 2-25 cm/s (500 nL/s to
144 injection of a solution at 4 bar pCO2 into a capillary tube packed with crushed calcite.
145 lute H2SO4 is formed on the top of two metal capillary tubes placed in a concentric annular arrangeme
146                                          The capillary tube provides the reference peak for quantific
147   Continuous-flow, microfluidic reactions in capillary tube reactors are described, which are capable
148 MP-2 and pericyte TIMP-3 expression leads to capillary tube regression in these cocultures in a matri
149 illary tube formation (morphogenesis) versus capillary tube regression in three-dimensional (3D) coll
150 folding of PI3K and Akt to alter endothelial capillary tube stability in vitro.
151 derived TIMP-3 are shown to coregulate human capillary tube stabilization following EC-pericyte inter
152               In vitro secretoneurin induced capillary tubes, stimulated proliferation, inhibited apo
153 he fovea, whereas en face OCT visualizes the capillary tubes surrounding the fovea regardless of thei
154          By pumping solutions through copper capillary tubes that are thermally anchored to heated an
155 iter and smaller liquid volumes inside glass capillary tubes that have an optically transparent thin
156 l migration by 42% and promoted formation of capillary tubes; these effects were blocked by a neutral
157 difference in pressure between two ends of a capillary tube through which the solution is flowing at
158                       Endothelial cells form capillary tubes through the process of intracellular tub
159 pinch-off dynamics of a bubble confined in a capillary tube undergo a sequence of two distinct self-s
160 ractions to be performed simultaneously in a capillary tube, using only 5 nL of sample and extraction
161  (aminoalkyl)silane-derivatized fused-silica capillary tube via a biotin/streptavidin/biotin linkage.
162 osited on the outside of glass melting point capillary tubes were analyzed in positive ion mode with
163 ween circulating cells and P-selectin-coated capillary tubes were measured.
164 es of capillary loops together into a single capillary tube where capillary isoelectric focusing (CIE
165  microsprayer, but with an extended sampling capillary tube which can reach into the depths of 96-, 3
166  x 127 microm inner diameter stainless steel capillary tube which was used to introduce gas into the
167 oscopy with standard instrumentation using a capillary tube with a secondary standard.
168                                 Fused-silica capillary tubes with 50-microm bores have been chemicall
169 croL serum pushed directly from self-sealing capillary tubes with a dispenser).
170 tion of a complex interconnecting network of capillary tubes with readily identifiable lumens.
171 roach for microarrays that uses fused-silica capillary tubes with tapered tips for printing pins and
172 was loaded into 150-micron-i.d. fused-silica capillary tubing with a pulled 5-10-micron needle tip at
173  minute-range flow through a 0.5-mm-diameter capillary tubing with as low as 250 mV of applied voltag
174 nt consumed by the conventional WB using the capillary tube without any need of special micromachinin

 
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