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Its job is to recognize chemical tags called methyl groups that get added to DNA at what are called CpG sites, and to recruit proteins that silence or switch off the genes at these regions.
The P13K-AKT pathway, upregulated on SLActive surfaces (in relation to angiogenesis), has also been implicated in neuronal survival and subsequent neural development [77,78] and could have contributed to upregulation of neurogenic genes at these surfaces.
For the genes at these extremes, it is likely that the ABA provides fairly accurate predictions of protein levels.
Owing to the large number of differentially expressed genes at these two time points, we narrowed our focus on the 72-hpf data set alone.
There are two alleles for genes at these loci: the "zero" and the "one" alleles, and proboscis length (as corolla-tube depth for flowers) is determined by the number of "one" alleles.
Most of the genes at these islands are required for meiosis [ 30, 32].
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However, only a moderate increase of the expression of these genes at the protein level was detected [8] [9].
We did not detect changes in the expression of these genes at the RNA level in PC12 cells.
The importance of other Group IV SERA genes in this lineage cannot be ruled out because of substantial expression of these genes at the blood stage [7].
The greatest activation of these genes at this time point was observed in the TCPH group.
The evaluation of the gene at these levels is the ultimate step in assessing their contribution to the trait of interest.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com