<p>Evaluation of the gap distance in migration assay of C666-1 NPC cells upon treatment as indicated.</p
<p><b>A</b>) ‘Wound healing’ assay. A confluent layer of L3.6pl was scratched and either left untrea...
<p>A, SKBR3 subclones migrated faster than parental SKBR3 cells. NAC was able to effectively inhibit...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
<p>Inhibition of CESCs migration were examined by increasing the numbers of NP cells loaded in the l...
<p>(a, b) NSK-01105 inhibited HUVECs migration by wound-healing assay. Cells were starved to inactiv...
<p>The number of pII (open bars) or MDA-MB-231 (solid bars) cells showing migration through agarose ...
The transwell chamber migration assay and CCD digital camera imaging techniques were used to investi...
<p>(A) Procyanidin A2, (B) procyanidin B1, and (C) morelloflavone. Inhibitors were used at 25 μM, 50...
(A) HUVECs were seeded until they reached 60% confluency and were treated with L-NMMA (50uM) or vehi...
<p>A–B, The subclones migrated faster than the parental cells SKBR3 cells (A) and 4T1 cells (B). NAC...
<p>(a) Treatment with a cGMP agonist (8-Br-cGMP, 1 μM) or PKG agonist (8-pCPT-cGMP, 1 μM) alone. The...
<p>Migration was measured by scratch assays of annexin A1 shRNA-transfected MDA-MB-436 (A) and MDA-M...
<p>A. Migrated cells as a function of SsnB concentration (0.1 to 100 µM). B. Migrated cells as a fun...
<p>The graphs illustrate the behavior of NBT-II cells treated with different test compounds and grow...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
<p><b>A</b>) ‘Wound healing’ assay. A confluent layer of L3.6pl was scratched and either left untrea...
<p>A, SKBR3 subclones migrated faster than parental SKBR3 cells. NAC was able to effectively inhibit...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
<p>Inhibition of CESCs migration were examined by increasing the numbers of NP cells loaded in the l...
<p>(a, b) NSK-01105 inhibited HUVECs migration by wound-healing assay. Cells were starved to inactiv...
<p>The number of pII (open bars) or MDA-MB-231 (solid bars) cells showing migration through agarose ...
The transwell chamber migration assay and CCD digital camera imaging techniques were used to investi...
<p>(A) Procyanidin A2, (B) procyanidin B1, and (C) morelloflavone. Inhibitors were used at 25 μM, 50...
(A) HUVECs were seeded until they reached 60% confluency and were treated with L-NMMA (50uM) or vehi...
<p>A–B, The subclones migrated faster than the parental cells SKBR3 cells (A) and 4T1 cells (B). NAC...
<p>(a) Treatment with a cGMP agonist (8-Br-cGMP, 1 μM) or PKG agonist (8-pCPT-cGMP, 1 μM) alone. The...
<p>Migration was measured by scratch assays of annexin A1 shRNA-transfected MDA-MB-436 (A) and MDA-M...
<p>A. Migrated cells as a function of SsnB concentration (0.1 to 100 µM). B. Migrated cells as a fun...
<p>The graphs illustrate the behavior of NBT-II cells treated with different test compounds and grow...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
<p><b>A</b>) ‘Wound healing’ assay. A confluent layer of L3.6pl was scratched and either left untrea...
<p>A, SKBR3 subclones migrated faster than parental SKBR3 cells. NAC was able to effectively inhibit...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
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