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This pathway is designed to sample the intracellular milieu and present the information to the CTLs trafficking the area.
In this study, a novel adipic acid biosynthetic pathway was designed by extending the cis,cis-muconic acid (MA) biosynthesis through biohydrogenation.
The in vitro artificial pathway was designed to balance the intrapathway consumption and regeneration of energy and redox cofactors.
A synthetic enzymatic pathway was designed for the deep oxidation of glucose in enzymatic fuel cells (EFCs).
Although the synthetic pathway was designed to achieve the balanced reduction and oxidation of NAD+ and NADH, the thermal decomposition of the cofactors was not negligible (Additional file 2: Figure S2).
The didactical pathway was designed to create a basis on which to build conceptual changes and new knowledge to make sense to evolutionary concepts, rather than/or before explaining the formal contents and assumptions of the theory.
Based on the metabolic analysis, a succinate and polyhydroxybutyrate (PHB) co-production pathway was designed and engineered in Escherichia coli MG1655.
A novel metabolic pathway was designed for the production of 3-aminopropionic acid (3-AP), an important platform chemical for manufacturing acrylamide and acrylonitrile.
The Pathway was designed to apply in all settings (high-, middle- and low-income countries, and in any type of health system).
Each ester fermentative pathway was designed as an exchangeable ester production module for generating two precursors− alcohols and acyl-CoAs that were condensed by an alcohol acyltransferase to produce a combinatorial library of unique esters.
The Expedited Access Pathway was designed as a new program for medical devices that demonstrated the potential to address unmet medical needs for life threatening or irreversibly debilitating conditions.
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