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These constitutively-expressed transcripts are likely involved in core molecular processes used to sustain life, as shown by the domains found within them.
The molecular processes used by each tumor appear to be linked to the drug used, but there is heterogeneity between individual tumors, even those with the same histological type, in the pattern and magnitude of response to the same drugs.
The molecular processes used by each tumor appear to be linked to the drug used, but there is also heterogeneity between individual tumors, even those with the same histological type, in the pattern and magnitude of response to the same drugs.
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Increasing sophistication in our ability to characterize genomics and gene expression will require advances in our ability to measure in vivo molecular processes using highly sensitive and specific imaging probes.
Thus, self-assembly of proteins is highly complex, and hence it is difficult to decipher the entire molecular process using static, nonvisualization, or ensemble-averaging approaches.
The main contribution of our article is FReDoWS, a workflow-based methodology to automate the molecular docking processes using a FFR model.
To identify families of genes that might have significant roles related to specific biological or molecular processes, we used the DAVID database to annotate the 6124 probes and categorize them by function.
It could be hypothesized that molecular differences in manufacturing processes used for the preparation of these two formulations or changes in structure, for example, in glycosylation of some residues, may lead to a different activation of cell cycle and may account for the different wound healing effect.
In vivo visualisation of locoregional physiological, biochemical and biological processes using molecular imaging can detect diseases in pre-symptomatic phases or facilitate individualised drug delivery.
The listed target transcripts from low temperature-responsive or tissue-specific miRNAs were further categorized according to molecular function and biological processes using gene ontology (GO) analysis.
These two processes use common molecular mechanisms for the rearrangement of the actin cytoskeleton necessary for both convergent extension (54) and epithelio-mesenchymal transition (EMT)/migration (55), respectively.
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