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To further elucidate these phenomena, we reasoned that the most effective approach would be to use a genetic tool which allows us to visualize the process of neurogenesis during the life cycle of Drosophila.
The dual objective of this study was, first to use a genetic tool enabling the expression of esterase genes in enological conditions and, second, to investigate the impact of O. oeni esterase gene expression during winemaking on wine aromatic profile.
The best way to address this question would be to use a genetic tool designed to delete Ntf3 gene in a tissue specific manner, targeting only the optic tectum, but to our best knowledge, such a tool is unfortunately not available at the moment.
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They used a genetic tool and PCR-based approach to amplify a tiny region of the genome in dozens of mice, some exposed to ECT-like electrical stimulation and some not, to compare the status of cytosine at similar stretches of DNA in brain tissue.
As activation of the Wnt/β-catenin pathway, as assessed by the expression of Wnt/β-catenin target genes, is restricted to the β-catnc clusters in both mouse and human ACP [ 29, 52], we used a genetic tool in mouse to enable their purification.
Due to low frequencies of transduction and pseudolysogen formation, CP-T1 has not been widely used as a genetic tool.
We report the generation of BAC transgenic flies of wrapper-GAL4 and demonstrate how these flies could be used as a genetic tool to understand MG biology.
Our data suggest that the multiple nested TEs in ALDH genes have some functional relevance in plant responses to environmental/abiotic stresses, and this feature can be used as a genetic tool to identify and characterize genes that are crucial for stress responses in monocots.
The SSRs in those studies were used as a genetic tool to investigate diversity in local germplasm collections.
Transposon-based mutagenesis has been prevalently used as a genetic tool in mycoplasmas to generate mutants of interest as well as to define essential genes required for survival [ 10– 10].
The method used represents a genetic tool which allows to optimise, wherever necessary, the parthenocarpic trait and to tailor the expressivity of the trait for the different needs of horticultural production.
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