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With the aid of experimental design, we developed and characterized nanoemulsionsfor parenteral drug delivery.
Using the mechanism-based drug design, we developed a new Ca2+/CaM antagonists based on the structure of HBC.
According to the proposed design, we developed the first fast AVS2 encoder, and named it as uAVS2.
Using rational drug design we developed a novel mono-nitro analog of PR-104A that is essentially free of this off-target activity in vitro and in vivo.
Using structure-based drug design, we developed compounds that bind to residues (Arg386/Glu282) ABL1 uses to switch between inactive and active conformations.
Under this study design, we developed weighted estimating procedures for model parameters in marginal multiplicative intensity models and for the cumulative baseline hazard function.
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Once we have the beginnings of a detailed design, we develop a full, and preferably prototyped, storyboard.
In Section "Optimal transmit strategies design", we develop the optimal transmit strategies for the OFDM-based multihop relaying system, including symbol loading and precoder design.
After investigating different materials and collector designs, we developed a prototype consisting of an array of selectively coated glass tubes mounted in a conventional flat-plate collector housing.
Motivated by time-series experimental designs, we develop a model of the act of measurement in the social sciences.
In the first design cycle we developed many different visualizations, with the intent that the most effective would be selected to be taken forward for further development.
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CEO of Professional Science Editing for Scientists @ prosciediting.com