Sentence examples for mimics compared to from inspiring English sources

All cell lines examined displayed superior attachment, proliferation, spreading, and survival properties on the MAP-based ECM mimics, compared to other commercially available cell adhesion materials, such as poly-l-lysine and the naturally extracted MAP mixture.

The relative luciferase activity of pMIR/ EP2-3′-UTRwt, but not that of pMIR/ EP2-3′-UTRmut, wasignificantlyly suppressed by miR-149 mimics compared to NC mimics.

Duplicate experiments consistently showed decreased migratory capacity of MDA-MB-231 cells expressing miR-124 mimics compared to MDA-MB-231 control cells and mock cells at 24 and 48 h.

The numbers of invading cells on the underside of the membrane were significantly reduced both in SW480 cells (Fig.  4a, P < 0.01) and SW620 cells (Fig.  4B, P < 0.01) when transfected with miR-217 mimics compared to those transfected with NC mimics.

Analysis of polyp expansion showed that polyps were more frequently retracted when corals were in contact with macroalgae or algal-mimics compared to controls or cage treatment; the frequency of polyp contraction was correlated positively with growth.

Radial force analysis of both thick- and thin-walled prototype variations generated less vessel distension and wall tension in a vessel mimic compared to a commercial device.

The percentage reduction of relative firefly activities in pmirGLO/3′-UTR + mimic compared to activities of pmirGLO + mimic transfections correlate with miRNA activity on the given 3′-UTR.

Interestingly, the increase in Igf1 levels in BAL fluids following bleomycin treatment was significantly blunted in the presence of miR-29 mimic compared to both saline and control-treated mice (Fig 3C).

In normoxia, both cell lines showed a marked increase in free radical production upon transfection of mimic-210 compared to mimic-control (Figure 3A).

To understand the differences between protein structure and dynamics in cellular mimics as compared to buffer, we measured spin relaxation parameters (R1, R2, nOe) which quantify the motion and interactions of the residues on timescales of μs to ms (R1, R2,) and ps to ns (nOe).

The leaves of the transgenic plants showed markedly increased dark staining at the sites of lesion mimics as compared to the leaves of wild-type plants after both 3,3-diaminobenzidin and nitro blue tetrazolium staining, indicating the accumulation of H2O2 and superoxides in the transgenic plants.