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We therefore further determined the expression changes of three key enzyme genes (P5CS, P5CR and ProDH) in proline biosynthetic and degradative pathways under dehydration (Table 3).
Using leukaemic Kasumi-1 cells with conditionally inducible CEBPA function (Pabst et al, 2001a), we determined the expression changes of 470 human miRNAs.
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However, it is hard to learn the local motions within the feature space to determine the expression changes of each face, since the way one person expresses a certain emotion is normally somewhat different from others.
In this article, we present a cohort study designed to determine the expression changes of PD-1 and PD-L1 in septic shock patients.
Differences of tag frequencies appearing in CO and DS libraries were used to determine the expression changes of genes in response to drought stress.
To determine the expression change direction, we used "greater" or "less" parameters in the one-tailed Fisher's exact test to find the up-regulated transcripts or down-regulated transcripts respectively.
While we are unable to determine if the expression changes observed for the profiled genes are directly or indirectly affected by Hfq, the protein still appears to play a role in their expression.
To determine whether the expression changes observed for some of these genes can account for a portion of the previously described olfactory acclimation [ 6, 7], we performed additional experiments.
To confirm these findings and to determine whether the expression changes were specific to DTT or a general response to ER stress, we treated S2 cells with another ER stress reagent, Tm (5 μg/mL), which inhibits N-linked glycosylation.
Since many of these genes are known to be found in stroma, we examined the expression level of an epithelial marker, Krt2-8 (Keratin 8), in the samples to determine whether the expression changes are due to the change in the epithelial component of the tissues.
To detect molecular changes, we determined the expression level of ecmA in DIF-1 stimulated amoebae of both species by quantitative RT-PCR.
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