Migration analysis displayed a significant reduction in the average velocity and trajectory of breast cancer cell locomotion compared to control, suggesting that bioengineered mouse ES cell microenvironments inhibited the proliferation and migration of breast cancer cells.
The statistical analysis displayed a significant correlation between MNA and MMSE (P<0.001), as did MMSE correlated with Activity Daily Living (P<0.001) and BI (P<0.05).
Cell cycle analysis displayed a significant change in the cell cycle distribution in response to IGFBP7 over-expression in both Jurkat and Molt-4 cells: significantly more cells were in G0/G1-phase and less apoptotic or in G2/M-phase.
Within the set of interactions identified from sensitivity analysis, seven TF pairs display a significant enrichment in co-binding using a stringent cut-off of P < 0.01.
Surprisingly, in the same type of analysis, STAT1 did not display a significant correlation to IFN score either (data not shown).
This analysis suggests that hubs and superhubs display a significant diversity of co-expression patterns in comparison to peripheral nodes.
This analysis identified 170 genes associated with HARs that display a significant loss or gain of binding sites in human compared with chimpanzee (TFBS divergence) (File S1).
The experiments display a significant NO reduction at downstream distances.
Tumours of the CNS often display a significant histopathological heterogeneity.
Heterozygous drep-2 ex13 mutants do not display a significant deficit.
