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Furthermore, since S. pneumoniae's macrolide-resistance acquisition by ribosomal structure modification can be viewed as an on/off mechanism [27], corresponding to resistant/susceptible bacteria, macrolide-susceptible and -resistant (SM and RM) strains were considered.
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These vectors form the foundation of the Plasmo dium genetic modification resource, PlasmoGEM, which can be viewed and requested through a searchable database at http://plasmogem.sanger.ac.uk (Schwach et al., 2015).
Yet, the considerations with regard to the moderating factors and modifications affecting intervention fidelity can be viewed in the broader context.
Recent studies on epigenetic mechanisms also provide a framework within which transcription factor activity, chromatin modifications, and gene expression patterns can be viewed at hierarchical levels to link genotype and phenotype.
Modifications done at UniProtKB/Swiss-Prot can be viewed by clicking the 'History' link on each page; for example, the changes made during the marathon for the Q54U87 record can be viewed by comparing annotation versions 28 and 29 of the dhkA entry, here: http://www.uniprot.org/uniprot/Q54U87?version=28&version=29.
This method can be viewed as a modification and improvement of some existing methods [15, 16] for solving the variational inequality problem and the hierarchical fixed point problem.
Working with the same three quality factors, we compare SI-UNIWARD with four other methods - the block entropy-weighted method of[10] (EBS), the NPQ[11], BCHopt[9], and the fourth method, which can be viewed as a modification (or simplification) of[9] or as[10] in which the normalization by block entropy has been removed.
Although radically different from those observed in the Chaetophorales and the Chaetopeltidales (O'Kelly et al. 1994), the flagellar apparatus of the Oedogoniales can be viewed as a modification of the cruciate arrangement of basal bodies, which appeared with the proliferation of the flagella (Moestrup 1982; Van den Hoek et al. 1995).
The modifications of these genetic associations by adiposity can be viewed in two possible ways.
These can be viewed as omitting certain modifications that are irrelevant to the particular purpose of the model and considering the others as a single collective modification, in a similar way to how the multiple Akt-modifications of FOXO were treated here.
Our iterative scheme studied in this article can be viewed as a refinement and modification of the iterative methods in [8, 9, 24].
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