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Now, to quantitatively test whether HY concentration was important in PDT treatment for inhibiting cell proliferation, we compared the photocytotoxicity of HepG2 cells treated with increasing concentrations of HY using a PrestoBlue cell viability assay.
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It is now possible to quantitatively determine the contribution of individual countries to global mean temperature change7,8 (GSMT).
Using the calculated stoichiometry and stability of Reactions (A1) and (A2), it is now possible to quantitatively evaluate the contribution of reduced sulphur species to the transport of gold in aqueous vapour at temperatures up to 365 °C.
Having determined all fitness values for all mutants along the AZT-resistance pathway, we were now able to quantitatively estimate the effect of epistasis on the relative abundance of the double mutants.
To further validate our results, we now turn to quantitatively compare the different methods on a genomic scale.
Further developments of these methods to include the effect of residual structure in unfolded states, as well as structure in partially folded amyloidogenic intermediates are now needed to quantitatively understand and predict protein aggregation processes in vitro.
Thanks to great technological progress over the last few years, it is now possible to quantitatively evaluate intraplacental blood circulation and placental volume by means of 3D Power Doppler and VOCAL technique.
However, recent developments in computational tribology [ 10] now make it possible to quantitatively link surface tribological aberrations with accelerated wear in individual cases.
Now, it is possible to quantitatively test the predictions of our model for the dependence of L eq ∗ on protein charge and salt concentration through similar competition assays in which NA length preferences are observed for proteins with charge altered by mutagenesis under different ionic strengths.
Until recently, evaluation of these defects was discussed only qualitatively, but the development of new imaging devices has made it possible now to assess defects in the RNFL quantitatively.
The major challenge is now to understand, not only qualitatively but also quantitatively, how these molecules and mechanisms act in concert to generate the complex patterns of neuronal connections that are found in the nervous system.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com