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As such, our present study aimed at employing the wasp-cockroach parasitic interaction to define the neural substrate responsible for the drive to initiate walking in insects.
In this study, we explored the relationships between cTnT concentrations and patients' characteristics and STE-measured echocardiographic parameters and evaluated the additional prognostic value provided by cTnT or a GLS ≥ −15% or their interaction to define their clinical usefulness.
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It should be noted that even under conditions obviously favouring microcystin binding to proteins this interaction was limited to a specific subset of proteins indicating a specific interaction to defined targets.
The system allowed data to be collected efficiently for the development of a rigorous design space that combined formulation factors, process factors, and their interactions to define a tolerance surface where risk of future product failure was significantly reduced.
The dead-end elimination and A∗ search algorithms were used here to find all low-energy single mutant variants, and corresponding structures of a G-protein heterotrimer, to measure changes in structural stability and binding interactions to define a protein fitness landscape.
In view of the significance of these protein-DNA interactions to cellular physiology, we modified the existing InterMine Interaction class, which describes gene-gene interactions, to define a new class named ProteinDNAInteraction.
For this batch of experiments, we use the MIPS network of protein protein interactions to define the relationships.
In this study of protein-DNA interactions, we considered three types of interactions to define a binding site: hydrogen bonds, water bridges and hydrophobic interactions.
Furthermore, our study highlighted the importance of the analysis of the epistatic interactions to define with more accuracy the influence of genetic variants in susceptibility to breast cancer.
It is the essential role of gene-gene interactions to define a trait implicating complex disease-related mechanisms, particularly when each involved variant only has a minor marginal effect.
Notably, the protein products of genes in these two modules do not form physical complexes, and thus could not be identified by methods that use protein protein interactions to define the modules.
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CEO of Professional Science Editing for Scientists @ prosciediting.com