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Although being adopted in selected industries, combinatorial screening technologies for thin film materials are still in their infancy.
In recent years, several cell-based screening technologies for the isolation of antibodies with prescribed properties emerged.
To assess female university students' attitudes toward screening technologies for ovarian reserve and their potential influence on career and family planning decisions.
There is a pressing need to develop and utilize high throughput screening technologies for the development of new materials, as material discovery has fallen behind the product design cycles in many sectors of industry.
To enable an efficient tracing of misused anabolic substances it is necessary to develop new screening technologies for a broad range of illegal drugs including newly designed xenobiotic anabolic agents.
As we move to implement changes, regulatory agencies and industry are beginning to adopt tiered approaches, which leverage high-throughput screening technologies for prioritization and read across, followed by interrogation of "hit chemicals" with more rigorous dose-response assessment either in fit-for-purpose human cell-based assays or with traditional in vivo tests.
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The advances in high throughput screening technology for discovery of target molecules and the accumulation of functional genomics and proteomics data at an ever-accelerating rate will enable us to design and discover novel biomolecules and proteins on a rational basis in diverse areas of pharmaceutical, agricultural, industrial, and environmental applications.
We hereby present a new screening technology for the high-throughput interrogation of protein-protein interactions in mammalian cells.
Thus, we believe that the strategy of using redundant libraries and focusing only on hits isolated multiple times will greatly increase the utility of this screening technology for the discovery of diagnostically useful antibodies.
The workflow described here provides a general paradigm for recovery and characterization of microbially derived genes and gene products based on genetic logic and contemporary screening technologies developed for model organismal systems.
A reason why cost-related aspects were not as meaningful may be the relatively low cost of the screening technologies and, for selected disorders, the high perceived effects from screening of newborns [ 42].
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