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Using fMRI and an optimized task-based paradigm, we have performed the most comprehensive developmental characterization yet reported of sensori-motor functional activity in the equivalent period to the mid-third trimester of human gestation.
For these and other reasons, biodiesel production has gradually grown in recent years, raising the need for new rapid and cost-effective analytical tools and technologies for developmental characterization and quality control.
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However, to avoid the possibility of confounding phenotypes, we used only the alleles l(3)70Da s4868 and l(3)70Da, which harbor smaller mutations affecting only the 5′ region of the Pex1 gene, for subsequent developmental characterizations.
Finally, and perhaps most importantly, our evaluations show the potential utility of an approach using neuronotypic cells in culture to screen suspected developmental neurotoxicants, enabling characterization of vulnerable stages, likely outcomes, and rank comparisons of related and unrelated chemicals.
In systems developmental biology where characterization of complexity of various time course data likely leads to address inference of temporal dynamic patterns from transcriptome, we are not often really interested in exactly how only a single gene is temporally differentially expressed at a particular time point or period.
We consider theoretical, methodological, and artifactual factors that influence characterization of developmental and adaptive changes in childhood.
Since HTS scores of these analogs best matched the target criteria and antiviral activity was highest in this group [19], we subjected them to further characterization and developmental efforts.
Nonetheless, executions of longitudinal mixed modeling algorithms are highly desirable and would provide a more complete characterization of developmental patterns.
For characterization of developmental expression patterns, RNA was extracted using STAT-60 and the Aurum Total RNA Mini Kit with on-column DNAse digestion, as described previously [ 83].
Among amphibians, the genus Xenopus offers unique opportunities for genetic investigations of inner ear structure and function due to the availability of a sequenced genome [ 43], and the thorough characterization of developmental stages [ 44, 45].
Therefore, developmental studies, including the characterization of zebrafish mutants, can provide a roadmap or blueprint to re-establish or augment cellular differentiation or tissue function to aid regenerative repair in vivo, or in vitro for the stepwise production and expansion of stem and progenitor populations for therapeutic cellular replacement strategies.
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