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In mammals the altered transgenerational phenotypes have been observed for generations (Skinner 2014a), with environmentally induced epigenetic transgenerational inheritance of phenotypic variation in plants being transmitted for hundreds of generations (Cubas et al. 1999).
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If this is the case, then one would expect even larger variability to be observed for future generations to come.
Additionally, gene targeting studies show that telomerase-deficient mice do not age rapidly; in fact, overt phenotypes are not observed for several generations [ 8].
Importantly, the changes induced by a transient exposure to TNF were long-lasting and observed for many generations after TNF withdrawal.
Those generations born after economic growth has achieved a certain level of national wealth may, however, benefit from better neonatal and postnatal nutrition and medical care [ 7- 9], thereby yielding better health outcomes in adult life than observed for previous generations.
Our data suggest that elevated C-circle levels could contribute to ALT, although the greatest levels of C-circles were observed for late-generation pot-2 that possess long telomeres and were wild type for telomerase.
Finally, even though recombinant protein expression in Pichia Muts strain could circumvent the deficiencies observed for the generation of VLPs in Mut+ strains, the slower methanol utilization phenotype requires long fermentation times to reach peak product concentrations.
The labelled structures appeared to be duplicated in dividing cells before segregating during cytokinesis (Fig. 5A), similarly to what was observed for the generation of a new Golgi stack in dividing trypanosomes [ 47].
Similar effects were observed for third-generation cephalosporin and fluoroquinolone use, i.e., an increase of 10 DDD per 1,000 patient-days on a certain month or 30 more treated patients, resulted in an increase in %MRSA by 4.99 after 12 months for third-generation cephalosporins and by 4.40 after 11 months for fluoroquinolones.
However, no aggregation behavior was observed for the higher generations (>G3).
These observations are consistent with the relaxed fidelity observed for the second-generation nitroTyr-RSs and the near perfect fidelity observed for the first-generation nitroTyr-RSs (when expression is conducted in the absence of nitroTyr).
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