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Our initial design was to fabricate a conduit with PSHU-RGD alone; however, PSHU-RGD nanofibers proved too brittle to be further processed into the desired conduit.
Our initial design of the V-shaped structure contains a corner part to improve the coupling between two nanorod branches, while we then find that the enhancement ability of the V-shaped structures is robust regardless of the shape and material of the corner part.
In this paper, we present our initial design for assessing the user's product-specific knowledge using the proposed innovative method for detecting it directly in a non-intrusive way without asking users to answer or fill out any types of questionnaires.
Figure 6 illustrates both how our initial design space consisted of these two devices created with two lines of code, as well as the increase to 540 Devices with the addition of two permute functions (four lines total).
The results for our initial design for the mechanism of drug combination synergy (Figure 1e) confirmed the proposed rationale: Gemcitabine serves as a drug establishing a baseline perturbation on the inter-module network, but Bortezomib could add a more focused perturbation on key gatekeeper modules which are linked to the checkpoint perturbation established by Gemcitabine (Figure 5d).
For example, our initial design was to include 1000 pharmacy staff from 50 hospitals across China.
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Our initial aim when designing the present study was to establish the map of GH1 gene SNPs in our adult control population with heights normally distributed within the entire normal range for further comparison with genotypes in our paediatric population with growth delay, variable response to GH secretion tests and adequate response to GH therapy.
Our initial physics design concept accelerates a ∼30nC pulse of Li+ ions to ∼3MeV, then compresses it to ∼1ns while focusing it onto a mm-scale spot.
Our initial experimental design utilized four ponds as replicates (to be able to control for a pond effect) to assess absolute growth over a 6-month period.
Because of large sequence differences among parasites, we excluded highly genetically divergent gene families, such as var genes, in our initial probe design.
In our initial MESA design, ligand binding-induced receptor dimerization results in proteolytic trans-cleavage of the target chain (TC) by the protease chain (PC), releasing a transcription factor (TF) previously sequestered at the plasma membrane.
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