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"The initial screening revealed no evidence of health issues.
Zebrafish screening revealed that 12b, and 12d caused developmental defects.
This screening revealed that bovine CXCR2 is a major target receptor for HlgAB, in addition to bovine CXCR4, and CCR2.
The antimicrobial screening revealed that 2-methoxyphenyl nitroimidazole enol 3i possessed stronger anti-P.
Long-term follow-up UL97 resistance screening revealed evidence for transient and compartment-specific UL97 mutations.
An extensive solvent screening revealed the superiority of amides as media for both synthesis and application of the Au0 nanocolloids.
Biochemical and functional assays revealed a mechanism of glucocorticoid resistance, and high-throughput screening revealed that an experimental compound can restore GC sensitivity.
During our BACE1 research efforts, fragment screening revealed that bicyclic thiazine 3 had low millimolar activity against BACE1.
Subsequent biological screening revealed that some compounds displayed low to moderate antifungal activity toward pathogenic fungi and low phytotoxicity.
Enzymatic kinetic screening revealed that compound 7 was a potent competitive inhibitor of human O-GlcNAcase (Ki = 185.6 μM).
Fragment screening revealed that tyramine binds to the active site of the Alzheimer's disease drug target BACE-1.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com