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1 yonic endothelial cells and fibroblasts in a cell migration assay.
2 tro were determined by ELISA and endothelial cell migration assay.
3 a vascular endothelial growth factor-induced cell migration assay.
4 al, lymphatic endothelial, and breast cancer cell migration assays.
5 r-induced proliferation, tube formation, and cell migration assays.
6  cell migration were validated in live tumor cell migration assays.
7 rmined by both scratch assays and trans-well cell migration assays.
8      However, in the polymorphonuclear (PMN) cell migration assay, a decrease in neutrophil migration
9                                              Cell migration assays also demonstrated that the Aebp2 s
10 r HRPE cells to HGF/SF was investigated by a cell migration assay and the specificity of this respons
11 aker chemotactic activity than SDF-lalpha in cell migration assays and does not interfere with produc
12 cle cells, and endothelial cells in vitro in cell migration assays and in vivo in murine carotid aneu
13 pes was analyzed with vascular smooth muscle cell migration assays and platelet aggregation analyses.
14 evaluated by linear scratch wound healing, a cell migration assay, and live cell motility GFP-trackin
15  to migrate toward SDF-1alpha in an in vitro cell migration assay, and SDF-1alpha treatment triggered
16 ing genetic fate mapping, cell birth dating, cell migration assays, and electrophysiology, we find th
17 se chemokine receptors in static and dynamic cell-migration assays at both the cellular and molecular
18 on and validation of a label-free, real-time cell migration assay based on electrical cell impedance
19  When placed with monocytes/macrophages in a cell migration assay, Bm-MIF inhibited random migration.
20                                              Cell migration assays combined with genetic and molecula
21 type placentas as measured in an endothelial cell migration assay, consistent with a reduction in exp
22                                              Cell migration assays demonstrate that ephrin-B ligands
23                                              Cell migration assays in which Matrigel density, fibrone
24 is of MCAM(KD) or ST6(O/E) melanoma cells in cell migration assays indicated that Gal-1 ligand-depend
25 samples, these effects were only observed in cell migration assays (infection: 98+/-28 vs control: 87
26                                              Cell migration assays performed with CTHRC1-overexpressi
27                                         Live-cell migration assays reveal that BMP4 induces breast ca
28                         Western analyses and cell migration assays revealed an inverse correlation be
29                                     In vitro cell migration assays showed that hepsin-cleaved Ln-332
30 adation assay combined with the phagokinetic cell migration assay, structure-function relationships o
31 rough the use of primary rat astrocytes in a cell migration assay, that Par6-PKCzeta interacts direct
32                                              Cell migration assays validated the prediction of functi
33                                  Endothelial cell migration assay was performed in a modified Boyden
34                            An on-chip single-cell migration assay was successfully demonstrated withi
35                      Using a microfluidic 3D cell migration assay, we found that the presence of macr
36 both time-lapse microscopy and the Transwell cell migration assay, we showed that UTP significantly i
37                                              Cell migration assays were conducted to assess the effec
38                             Cytotoxicity and cell migration assays were used to determine the effect
39 tituted basement membrane in two-dimensional cell migration assays, whereas antibodies against beta1,
40                                              Cell migration assays with lung and thyroid cancer cells

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