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These observations hint that the evolutionary processes underlying genomic structures and OGPs in particular are complex.
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To date, the sequences excised from copepods have not been analyzed using large-scale genomic datasets, and the processes underlying germline genomic gigantism in this clade, as well as the functional significance of chromatin diminution, have remained unknown.
To date, the DNA excised from copepods has not been analyzed using large-scale genomic data [ 16, 17], hindering in-depth study of the processes underlying germline genomic gigantism in this clade, as well as the functional significance of chromatin diminution.
We perform detailed bit-string simulations of viral evolution that consider large genome lengths and incorporate the key evolutionary processes underlying the genomic diversification of HIV-1 in infected individuals, namely, mutation, multiple infections of cells, recombination, selection, and epistatic interactions between multiple loci.
This process may occur through environmental modulation of gene expression (without alteration of the underlying genomic sequence) in a process known as 'epigenetics' [ 8].
We demonstrate that these annotations can be used to infer nucleosomal states with distinct correlations to underlying genomic features and chromatin-related processes, such as transcriptional start sites, enhancers, elongation by RNA polymerase II and chromatin-mediated repression.
Therefore, investigation of the pathways related to cell cycle control and DNA damage response will help to understand the process of hUC-MSC passaging and the molecular mechanisms underlying genomic stability.
During those processes, the structure of chromatin must be dynamically and reversibly altered to enable or repress the access of cellular machineries to underlying genomic sequences.
In mesenchymal stem cells (MSCs) GATA2 blocks adipogenesis, but its biological relevance and underlying genomic events are unknown.
And, these defects may be system wide, due to underlying genomic and environmental factors, but have more evident consequences in brain, with its high energy-requirements.
Quantitative protein expression data can offer valuable insight into underlying genomic, transcriptional, and post-transcriptional regulatory activity, as well as a more representative view of the disease phenotype.
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