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Free Mn2+ in cytosol has greater access to water to induce more T1 shortening compared with mitochondrial Mn2+.
All cancer cells have shown significantly greater T1-value shortening compared with normal cell (p < 0.001) (Table 2).
The addition of BPA to the rapid magnetic relaxation switch immunosensor led to transverse relaxation time (T2) shortening compared to a blank control as shown by NMR relaxometry measurements.
Following TQ (25 µM) treatment for 15 days, M059K cells showed greater telomere shortening compared to M059J cells (Figure 4E).
Before TAC, ankyrin-B+/− mice displayed a modest, but significant 10% increase in percent fractional shortening compared to wild-type mice (wild-type = 58.3±1.9%, n = 16; ankyrin-B+/− = 63.9±1.5% n = 15 mice; p<0.05; Figure 2D).
After TAB, the miR-499 transgenic mice displayed more severe contractile dysfunction as indicated by the decline in fractional shortening compared to control mice (Fig. 7C, Table 1) that underwent the same degree of TAB (peak aortic pressure gradient: WT 49±10 mmHg, TG 43±9 mmHg, p = 0.251).
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Tail-off time in case of MnO2-mixed PbO is considerably shortened compared to that of MnO2.
Because of the fast blood and renal clearance of the monomeric bisphosphonates, the time scale for target accumulation is shortened compared to the dimeric compounds.
For example, time for apatite induction in the 1.5-fold SBF was significantly shortened compared to that in the standard SBF.
For the H2O2 treated MWNT (thermal drying), the length of the MWNT was shortened compared that of the H2O2 treated MWNT (freeze drying).
With the QC formed with electric heaters, the charging time at the early and middle stage is obviously shortened compared with that of the experiment without electric heating.
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