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Immunocytochemical analysis showed a clear decrease in the intensity of ER staining in the nuclei of MCF-7 cells treated with either E2 or with FTI-277, or both, with a concomitant decrease in cytoplasmic ER staining.
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Upon dehydration, there is a clear decrease in intensity for the main peak, and a contraction in the first shell Sn−O distance from 2.0 to 1.95 Å.
When oligomeric αS, LUVs and DPX were mixed at the same time, a clear decrease in fluorescence intensity was observed.
The spectra showed a clear decrease in fluorescence intensity and a further red-shift from 351 nm to 361 nm was observed as the GdnHCl concentration was raised from 1.75 to 4 M.
Interestingly, further increasing the glucose concentration to 67 mM and beyond results in a clear decrease in both the recorded fluorescence intensity and the hysteresis of the F-CV.
Incubation at 37°C of serum-starved cells stimulated with fMLP induced a clear decrease in cell surface fluorescence intensity after both 10 and 30 min internalization.
Visually, there was a clear decrease in staining for GFAP (Fig. 6E,F), and a quantitative analysis of fluorescence intensity confirmed that SB505124 treatment significantly decreased GFAP expression in the damaged SVZ (Fig. 7G, p<0.05).
A clear decrease of the signal intensity was observed when the SiO2/Si substrates were immersed for 1 or 4 h.
In the KW-2478 and bortezomib combination groups (Groups 5 and 6), clear decreases in GFP fluorescence intensity were seen compared with the control group, and compared with mice treated with bortezomib or KW-2478 alone.
Lignin removal is also clear from DRIFT measurements, which show a decrease in the intensity of the lignin main peak at 1510 cm-1 (see Figure 1A in Additional file 2).
With PE, penetratin induced also a relative decrease in the intensity at 490 nm.
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