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Enterococcus faecalis ATCC 29212 and Staphylococcus aureus ATCC 43300 (MRSA) were resistant to the eluate of both samples at day 7, and further testing was discontinued.
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Engraftment was successful for both samples, starting at day 57 post-injection for samples obtained at R1 (74.7±16.1 blasts/μl of blood) and at day 72 post-injection for samples obtained at diagnosis (11.4±3 blasts/μl of blood, as compared with 146±58.6 blasts for samples obtained at R1), and both progressed then after.
Microbiological and physicochemical analysis was conducted for both HHP and control samples, at day 0 (right after the HHP treatment) and after 7 days of storage.
The rapid down-regulation of miRNAs in both wounded and fungus inoculated samples at day 1 was significant for PamiR3693 and PamiR3705.
The number of viable cells as assayed by MTS was higher in loaded samples at day 10 but there was no difference by days 15 and 20.
No melanosis was observed in all samples at day 0, regardless of pre-cooking time.
There were no differences in rancidity between all samples at day 0 of storage (p > 0.05).
Tissue growth involved volumes either inside or outside samples at day 21 for L1, suggesting cyclic stimulation is a trigger for delayed proliferative response of cells.
Fig. 7 a Digital photo of tumor with treatment of different samples at day 32, (b) tumor volume vs. time profile.
To describe optimization of a nationwide newborn screening program for cystic fibrosis (CF) that combines an immunoreactive trypsinogen (IRT) assay and DNA mutation analysis in dried blood samples at day 3.
To identify the T-RFs, the AOA and AOB clone libraries from all the soil samples at day 28 were constructed with same primers CrenamoA23f/616r and amoA-1F/2R used in the qPCR analysis, but the different enzyme.
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