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In this paper, two-dimensional plane strain finite element analyses of the active repair for cracked structures by using multi-layered piezoelectric patches have been studied.
Analyses of the active site architecture, in conjunction with mechanistic studies and precedent from the nucleotide diphosphate hexose dehydratases and other systems, suggest a novel mechanism of glycoside hydrolysis by GlvA that involves both the NAD(H) and the metal.
Structural analyses of the active compounds were performed by LC-MSn.
Similar to human PP1 and Glc7, λ-PPASE (a bacteriophage ortholog of PP1) shares this conserved catalytic domain and has been previously examined in structure-function analyses of the active residues in the catalytic pocket.
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To help with discovery of PDE9 inhibitors, we performed mutagenesis, kinetic, crystallographic, and molecular dynamics analyses on the active site residues of Gln453 and its stabilizing partner Glu406.
To fill this knowledge gap, we have undertaken structure/function analyses of the DinB active site and have gained insights into the active site residues that govern bypass and fidelity of different lesions.
In order to study the photodegradation kinetic and to optimize the chromatographic parameters we started with the analyses of the pure active principles.
Thus, the analyses of the DinB active site and its aromatic triad have provided insights into mechanisms that govern both TLS and the fidelity of the bypass of different cognate lesions.
For QTL analyses, the start of the active emergence was designated as day one.
Table 5 reports bivariate analyses of the relation between active acceptability and respondent characteristics.
The force analyses of both active and passive overconstrained PMs belong to the statically indeterminate problem.
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