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Process description categories are hence only left blank, if for all 17 model organisms there is no description in this category.
Despite the usefulness of model organisms, there are no published reports that specifically address the role of the secretory pathway in generating toxic amyloid species.
However, compared with humans and other model organisms, there is limited research on the extent and impact of CNVs in the chicken genome.
Although the calpain family is well characterized in animal and plant model organisms, there is a great lack of knowledge about these genes in unicellular eukaryote species (i.e. protists).
However, given the extent of sex-differentiated genetic architecture in model organisms, there is no reason to believe that heterogeneity in allelic effects between males and females will not also exist in humans.
Application of Tiling Assembly on A. thaliana, D. melanogaster, C. elegans, and S. cerevisiae identified hundreds of high-confidence novel genes, demonstrating that even in the most well-studied model organisms there are still undiscovered genes.
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Despite the importance of Mnemiopsis as an emerging model organism, there were no high-quality genome-scale sequence data available for any ctenophore species until recently.
In addition to the use of Listeria as a model organism, there is great interest in studying this organism because of the increasing incidence of listeriosis in the United States of America (USA) and Europe [ 23, 24].
These artificial boundaries might bias the results of animal dispersal models by creating artificial barriers to movement for model organisms where there are no barriers for real organisms.
The main effort has been done in a number of model organisms, but there are plenty of other higher eukaryote genomes that will need promoter identification.
Since most of these plant genera do not include model organisms, normally there are no available annotated reference genomes for comparison, hampering the location of the EST-SSRs within the genome.
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