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Therefore, the consistent behavioral and ERP results between Experiment 2a and 2b suggest that the non-automatic extraction of irrelevant orientation is not due to the information decay of the gap orientation from VWM. Besides, The absence of automatic extraction in Experiment 2a and 2b may be alternatively related to the unbalanced change signal between the two types of information.
Remarkably, the conventional intrinsic apoptosis pathway controlled by the Bcl-2 family did not show an unbalanced change.
Insertion/deletion (indel, unbalanced change <100 bp) and copy number variation (CNV, unbalanced alteration 100 bp upwards) are increasingly observed to be important in development and disease (Lee and Scherer 2010; Weischenfeldt et al. 2013).
As we discuss later, elucidation of the specific mechanisms by which control is manifest in mtDNA populations will require further research, but these numerical experiments attempt to represent the cases where a perturbation is naturally compensated for (matched changes, Figure 5A) and where it is not (unbalanced change, Figure 5B).
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When trade policy shocks result in unbalanced changes in imports and exports, the original trade balance is then restored by implicit exchange rate adjustments.
Copy number variations (CNVs) are unbalanced changes in the structure of the genome and include deletions, insertions, and duplications of >1 kb in size [ 43].
SGCZ (14.6 Mb), although disrupted by two unbalanced changes and one balanced translocation breakpoint, is unlikely to be a cancer gene.
Importantly, the unbalanced changes in the eEF1H subunits content were observed in the vast majority of the tumor samples (Table 1).
Using array-based strategies, it is possible to identify unbalanced changes, that is, net gain or loss of large segments of DNA.
Global unbalanced changes are expected due to small array size and gene selection based on pathways predicted to be involved in a particular response.
It is speculated that it is these changes and the unbalanced changes in many {S}, not a dominant change in a small number of {S}, that may lead to the disease phenotype.
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