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Several stop-word lists were analyzed for their ability to improve system performance, viz.
The diabodies were analyzed for their ability to bind both immobilized and cell surface-bound αvβ6.
All collagen variants were analyzed for their ability to assemble into D-periodic fibrils.
DB were analyzed for their ability to induce virus neutralizing antibodies and cytotoxic T cells (CTL) after immunization of mice.
A number of 5-phenylisoxazole-3-carboxylic acid derivatives (5a e, 11a e) were synthesized and analyzed for their ability to inhibit xanthine oxidase.
Microsomal preparations isolated from ASO- and RSO-treated cells were analyzed for their ability to convert PGH2 to PGE2 in the presence 2.5 mM reduced glutathione.
The 22 analogues were analyzed for their ability to serve as agonists at GPR55 and valuable information for both ends of the molecule was ascertained.
In this study, supernatants from LPS/ATP-stimulated human monocytes were analyzed for their ability to induce IFNγ production by KG-1 cells.
Single amino acid-substituted analogs of pCDR3 were designed and analyzed for their ability to stimulate or inhibit the proliferation of a pCDR3-specific T-cell line.
Sera obtained from mice immunized with rOmpF plus adjuvant or PBS plus adjuvant were analyzed for their ability to promote opsonophagocytic killing of E. coli CVCC 1515 by murine peritoneal macrophages.
All possible overlapping nonameric peptide sequences from 52 secretory proteins were generated in silico and analyzed for their ability to bind to 33 alleles belonging to A, B and C loci of HLA class I. Fifteen percent of generated peptides are predicted to bind to HLA with halftime of dissociation T1/2 ≥100 min and 73% of the peptides predicted to bind are mono-allelic in their binding.
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CEO of Professional Science Editing for Scientists @ prosciediting.com