We adapted this experimental model to adolescent rats.
We adapted this technique and applied it with success to predict work-related musculoskeletal disorders.
We adapted this assay to a 96-well plate format, quantifying GFP expression with a fluorescence scanner.
We adapted this method to estimate the total discharged mass using each of 17 isopleth contour lines (Table 1; Fig. 5).
For a comparison with Cottrell and Letrémy [7], we adapted this approach to obtain a simplified algorithm ImpSOM in the previous section.
We adapted this assay to allow screening of mutant libraries of either l- or d-amino acid specific aminotransferases in a continuous fashion.
Here we adapted this approach to develop a high throughput mechanical screening (HTMS) system capable of measuring the mechanical properties of up to 48 materials simultaneously.
We adapted this system for PCC 7002 and achieved conditional and titratable repression of a heterologous reporter gene, yellow fluorescent protein.
In this study, we adapted this method to an on-line setting to collect information about young adults' life histories, sexual behaviors, and substance use.
Here, we adapted this assay to develop intrabody selection after Tat export (ISELATE), a high-throughput selection strategy for the identification of solubility-enhanced scFv sequences.
As a proof of principle, we adapted this strategy for the detection of DNA sequences that are diagnostic of two pathogens (drug-resistant tuberculosis and Escherichia coli) by using methylene blue-labeled structure-switching DNA stem-loop.
