Sentence examples for figures were analyzed by from inspiring English sources

The figures were analyzed by a University of Texas mathematics professor.

Images and figures were analyzed by Image-Pro 6.0 software (Media Cybernetics, USA).

Images and figures were analyzed with MPI (Siemens Corridor 4DM V501) and reviewed by a nuclear physician and cardiologist together.

Wound healing and tubule formation in figures five and six were analyzed by using 2 controls, 3 scNT-N and 6 scNT-MUC samples with three replicates and the statistical significance was calculated by ANOVA and confirmed by Duncan's multiple range procedure.

To determine whether reprogrammed neuronal cells acquired a genuine neuronal identity, cells transduced with the most efficient combinations of target genes (ND4+I, ND4+P, and ND4 as control; Figures 4B 4D) were analyzed by patch-clamp recording at 28 35 DPI after a 2-week co-culture with cells derived from cerebral cortex at embryonic day (E 14.5.

Similarly, the induction of the c-Fos and c-Jun proteins in response to NGF stimulation (Figure 3E,F), and p38 and JNK phosphorylation in response to anisomycin treatment (Figure 3G,H) were analyzed by both techniques.

The PCB 2,2,2-trichloroethyl sulfate diesters 1 10 and selected, structurally-related methoxylated PCBs 11 and 12(Figure 1) were analyzed by electron ionization mass spectrometry (EI-MS).

In order to evaluate the capacitance due to the Al oxide layer at the Al/PCMO interface, the observed impedance spectra shown in Figure 5 were analyzed by comparing with the simulated spectra constructed on the basis of an equivalent circuit composed of parallel connection of resistance and capacitance (RC).

The response studies shown in figure 4a were analyzed by one-way ANOVA.

To examine the effects of PyLT on the expression of proteins that could contribute to antiestrogen resistance, LT-5 cells harvested in parallel to those shown in Figure 3A were analyzed by immunoblotting for PyLT and for cell cycle regulators including cyclins A, E and D1, and the cdk inhibitors p21 and p27 (Figure 3C).

Eight genes from the cluster I of Figure 2 were analyzed by qRT-PCR.