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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.
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.
21 type placentas as measured in an endothelial cell migration assay, consistent with a reduction in exp
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
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
36 both time-lapse microscopy and the Transwell cell migration assay, we showed that UTP significantly i
39 tituted basement membrane in two-dimensional cell migration assays, whereas antibodies against beta1,
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