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Our lab and others have observed that for a wide variety of proteins, peptide-level calibration approaches resulted in significant quantitative bias when examined with protein-spiked QC samples.
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We used positional cloning to identify candidate ozone-susceptibility genes in a significant quantitative trait locus (QTL) on mouse chromosome 7 (Inf2) (Bauer et al. 2010; Kleeberger et al. 1997), including histocompatibility genes and Tnf, which are involved in innate immune function.
In an early study, Schwende et al. [20] concluded that while there seemed to be no specific volatile products that could be related to genes in the MHC, significant quantitative differences in several secondary metabolites could be observed in females of different MHC haplotypes.
Our analyses demonstrate that partial interference considerations can result in not only significant quantitative differences in the predicted system capacity but also fundamental qualitative changes in the shape of the stability region of the systems.
This is because such considerations can result in not only significant quantitative differences in the predicted system capacity but also fundamental qualitative changes in the shape of the stability region of the systems.
This is because such considerations can result in not only significant quantitative differences in the predicted system capacity but also fundamental qualitative changes in the shape of the stability region of the systems (e.g., from a concave to a convex region).
Despite the genetic evidence implicating these sequences and their biologically pertinent in vivo behavior we observed no significant quantitative difference in the in vitro activity displayed by the alternative alleles of the SZ- associated SNP, rs379266.
In this manuscript we identify significant quantitative and qualitative changes in chromatin distribution in field and early carcinogenesis.
Monitoring both the germ tube formation and growth on CHROMagar we confirmed that the species used showed expected phenotypes e.g. only C. albicans and C. dubliniensis formed germ tubes at 37°C in the presence of serum with significant quantitative difference in germ tube formation between C. albicans and C. dubliniensis (data not shown).
Although there was qualitative agreement between radiotracer uptake, TUNEL flow cytometry staining and clonogenic survival data in these in vitro studies, there were significant quantitative differences.
Bacterial 16 s sequences were found in all subjects, without significant quantitative differences between groups.
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