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Elucidating the cellular and molecular basis of fiber elongation could identify potential targets for genetic manipulation of fiber length.
While the presence of PMD in the source arm can result in the generation of image artifacts, we have demonstrated that these artifacts can be mitigated by careful manipulation of fiber polarization controllers.
Thus, molecular genetic studies of the stage-by-stage process of ovule development is important for understanding molecular mechanisms of fiber development and the goal of effective manipulation of fiber characteristics.
This included physical manipulation of fiber and grain particle size [ 8, 11, 12], the inclusion of antibiotics in the diet [ 13], the use of yeasts and probiotic bacteria [ 14, 15], and the addition of dicarboxylic acids [ 16], flavonoids [ 17] or essential oils [ 18] to manipulate rumen microbial communities and subsequently ruminal fermentation.
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Odor emissions were successfully assessed, and manipulation of dietary fiber has the potential to influence CH4 and NH3 emissions.
Thus, Set 1 genes may be key to the successful genetic manipulation of cotton fiber traits.
Finally, the effective transcriptional regulation afforded by DiSTRES could be combined with current methods of transductional regulation including manipulation of Ad fiber knob [ 18- 24] and use of bi-specific antibodies [ 25- 29] to further improve the targeting of gene therapy vectors to specific cell types and therefore increase the specificity and the safety of the vectors.
The large displacement amplitude has a number of potential applications, including the switching or manipulation of optical fibers.
This study establishes a foundation for elucidating the molecular mechanism of the mutated gene and genetic manipulation for the improvement of fiber fineness and maturity.
This reflects the fact that due to the longer working distance, the manipulation of a microlens tipped fiber is easier and more stable when compared to an axicon tipped fiber.
This study focused on the manipulation of electrospun scaffold architecture (via control of fiber alignment) and porosity (via inclusion of a sacrificial fiber population) to control cellular interactions in vitro as well as cellular population and matrix organization in vivo.
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