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Techniques and assays for screening of small molecules with potential to modulate microRNA function and or action [16] apart from phenotypic or specific expression based screens have been increasingly being adapted for high-throughput screening strategies.
Many detergent based screens have been performed in the context of membrane protein structural biology.
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In addition, poor compliance with selective risk factor based screening has been reported [ 29], so that not all colonized patients may have been detected.
A polymerase chain reaction based screen has been used to identify PI3Ks in the human breast using mRNA derived from cells and epithelial tissue from reduction mammo-plasty.
Currently, genetically encoded, sensor-based screens have been developed for AKG [ 40] and arginine [ 50], and a direct ethylene sensor could potentially be constructed based on the ethylene receptor in plants and cyanobacteria [ 51].
While cell-based screens have been used in purely empirical screening efforts, they can also be used as the basis of target identification or verification.
To overcome this problem, cell-based screens have been incorporated into the drug discovery process.
Cell-based screens have been widely used in drug discovery although historically, these assays are conducted using genetically diverse cell lines derived from human tumors [1], [2].
Viral-based screens have been introduced for their promise in expanding RNAi screens to models incompatible with conventional siRNA-based approaches.
High-throughput RNAi-based screens have been successfully used to identify synthetic lethal pathways with well-characterized tumor suppressors and oncogenes.
As in other anti-infective areas, target-based screens have been unsuccessful prompting investigators to adopt whole cell screening once more (Cole & Riccardi, 2011; Payne et al, 2007).
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