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To rapidly identify anti-SARS drugs available for clinical use, we screened a set of compounds that included antiviral drugs already in wide use.
We screened a set of GMREP (Glass Multimerized Reporter Enhancer Promoter) lines ([22]; [23]) and identified 86 lines that uniquely modify different subclasses of genes.
To further study the Aβ binding pattern of endogenous anti-Aβ antibodies having the IgM isotype, we have screened a set of plasma samples from healthy donors.
To gain further insight into more preciously reprogrammed genes specific to SR3, we screened a set of genes to select 31 genes that were specifically expressed in SR3 (Figure 2B and Table 3).
We screened a set of 27 breast tumors to determine our ability to measure HER23D, HER3P and HER3PI3K in tumors and to ascertain the utility of such measurements in a clinical setting (Figure 3A).
To study the involvement of LRR RLKs in root development and in the Arabidopsis-H.arabidopsidis compatible interaction, we screened a set of homozygous LRR RLK T-DNA insertion lines.
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In this study, quantum chemistry calculations were used to screen a set of twelve representative functional groups by comparing their CO2 and CH4 binding energies, as well as the binding energy differences.
We have also used the predicted models to screen a set of novel molecules identified as miRNA inhibitors derived from different literature sources [14 16, 26, 27].
The 4020 fragment was used as a probe to screen a set of filters of the L. donovani LSB-51.1 genomic cosmid Stuartlab-Cos library (gift of Drs T. DeVos, P. Myler and K. Stuart).
Our laboratory employed an adapted SYBR Green assay in microplate format to screen a set of crude extracts from marine microorganisms for their ability to inhibit parasite growth in culture.
By screening a set of BAC library filters, three RpoT genes were identified.
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