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Secondly, P1606S occurred at a very low frequency at 44 DPI followed by nondetection in 57 DPI (perhaps due to extremely low frequency of occurrence), indicating the possibility that it is an individual deleterious mutation, which restricts the fitness or success of the escape variant.
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Modifying native organism through evolutionary engineering for desirable purpose often provides great breakthroughs to challenging obstacles in areas within biotechnology including biofuel production, screening of desirable phenotypes, etc. Conventional mutation methods, however, can be biased to certain types of mutations which restrict the accessibility to desirable phenotypes.
DOI: http://dx.doi.org/10.7554/eLife.06492.016 In the reverse evolution, the active site architecture necessary for phosphotriesterase activity was restored largely through new mutations, which restricted the reversion of mutations accumulated in the forward evolution.
The pRP1345 construct contains the transposase gene under the control of the proximal protamine 1 (promoteromoter, which restricts expression to spermatogenesis and limits transposon mutations to the germline, thus preventing somatic mutations (Fischer et al. 2001).
One of these previous studies used mathematical modeling to substantiate this possibility [71]; however, the analysis was confined to the contribution of the CCR5-Δ32 mutation, which is restricted to individuals of European descent.
Republicans are also busily passing laws which restrict registration efforts, restrict early voting, restrict poll locations, and restrict ballot-box access in many other ways.
Another factor might be enhanced pro-angiogenic properties of CRC cells with KRAS mutation which, however, might be restricted to certain KRAS mutation subtypes [ 32, 34].
Bioinformatic analyses have predicted that the human pathogenic mutations, which are not restricted to a specific domain or region within the enzyme, could affect the substrate binding site or the dimerization interface of TPI [2], [13].
We have sequenced the sex-related locus in eleven different E. cuniculi isolates, however, and found them to be highly conserved with the exception of a few point mutations, which tellingly are restricted to the flanking genes and are not found in the HMG or weak HMG genes (Figures 3 and 4).
Both conditions are caused by a single DNA mutation, which makes them relatively easy to detect.
Hence sex is the perfect complement to mutation, which engenders novel genes.
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