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Zebra finches were trained with sequences differing in transitional and positional information and next tested with novel strings sharing positional and transitional similarities with the training strings.
We next tested with a specific μOR agonist [D-Ala2, N-MePhe4, Gly-ol]-enkephalin (DAMGO).
The marker genes were next tested with qPCR in the same O3 samples used for CRK expression.
The influence of proteasomal degradation on MMP activity was next tested with the proteasome inhibitor lactacystin (Fig. 3C).
The two candidates, BTD and GPX3, confirmed by this approach were next tested with immunoblot assay in a blinded set of breast cancer and control to ascertain the markers ability to differentiate the two groups.
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We next tested GeneStitch with the artificial community dataset.
We next tested models with positive feedback (PF, k0 = 1 and k1 = 10) using 2D simulations in which the cell was represented as a circle.
DOI: http://dx.doi.org/10.7554/eLife.05472.006 In order to assess the role of relative motor number on competitive outcome, we next tested scaffolds with varying ratios of myosin V and myosin VI motors (xV: yVI; Figure 3 figure supplement 1) on 2D actin networks.
We next tested the cells with an in vitro glucose-stimulated insulin secretion assay, to assess their function.
Being engineers, the cat-lapping team next tested its findings with a machine that mimicked a cat's tongue, using a glass disk at the end of a piston to serve as the tip.
We next tested for interactions with actin cytoskeleton regulators.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com