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Known motifs in AgtGS predicted to play a role in catalysis and/or binding were compared with SSs analysed.
The SAR found for hemoglobin binding were compared with the SAR found in the literature for mutagenicity, carcinogenicity, and cytotoxicity of arylamines and nitroarenes.
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The specificity of binding was compared with the binding of the antibodies to recombinant pro-OP-1 pro-OP-1 pro-OP-1
This list of genes associated with significant changes in STAT3 binding was compared with the list of genes with significant expression changes using the online tool Galaxy (Giardine et al. 2005; Blankenberg et al. 2010; Goecks et al. 2010).
The hexapeptide cocaine complex was docked with different scoring functions combinations and resulting binding scores were compared with the SPE results.
Structures of newly synthesized compounds were docked into active site of COX-2 enzyme PDB: 1CX2, 3.0 Å X-ray resolution and plausible binding modes were compared with standard drug Celecoxib.
Fluorescent binding patterns were compared with pictures in [21] and with reference pictures provided with the Antibodies, Inc. kit.
Fluorescent binding patterns were compared with pictures in von Muhlen and Tan [21] and with reference pictures provided with the Antibodies, Inc. kit.
The generated RXRα binding data were compared with the data for RARα, PXR, LXR, FXR, and PPARα.
To this end, gastrula and early tail bud Xbra binding profiles were compared with Xbra/Xbra3 loss-of-function analyses at the early tadpole stage.
However, when the receptor-binding data were compared with circulating levels of gonadal steroids separately for each phase of the cycle, several significant correlations emerged.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com