Academic literature on the topic 'Greenscreen'

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Journal articles on the topic "Greenscreen"

1

Simpson, Kate, Nicola Bevan, Paul Hastwell, et al. "The BlueScreen-384 Assay as an Indicator of Genotoxic Hazard Potential in Early-Stage Drug Discovery." Journal of Biomolecular Screening 18, no. 4 (2012): 441–52. http://dx.doi.org/10.1177/1087057112470858.

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High-throughput cell-based techniques that permit early detection of compound-induced genotoxic damage have recently become available. Methods based on induction of the GADD45a promoter are attractive because multiple intracellular mechanisms that detect genetic damage intersect at this checkpoint gene. Consequently, assays such as GreenScreen HC, which uses p53-competant human TK6 lymphoblastoid cells and a GADD45a-GFP reporter, have been developed. GreenScreen HC allows weekly testing of dozens of compounds using 96-well microplates, with high interassay consistency. BlueScreen HC is a recent advancement, coupling GADD45a to Gaussia luciferase, with several advantages over GADD45a-GFP including the potential for miniaturization. Here we describe implementation of a 384-well BlueScreen assay. For drug discovery programs carrying out iterative analogue synthesis around a chemical lead series, these assays permit assessment of compound genotoxic potential in parallel to, rather than subsequent to, determination of activity at a therapeutic target. We demonstrate comparability of BlueScreen-384 to GreenScreen HC and illustrate the use of BlueScreen-384 to explore the structure-activity relationship around a genotoxic lead molecule to identify nongenotoxic analogues. BlueScreen-384 can reduce the need for costly and time-consuming analogue testing in more traditional genotoxicity tests, such as the Ames test.
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2

Perkins, Miriam Y. "Greenscreen teaching: Institutional instability and classroom innovation." Teaching Theology & Religion 20, no. 4 (2017): 343–55. http://dx.doi.org/10.1111/teth.12407.

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3

Walmsley, Richard M. "GADD45a-GFP GreenScreen HC genotoxicity screening assay." Expert Opinion on Drug Metabolism & Toxicology 4, no. 6 (2008): 827–35. http://dx.doi.org/10.1517/17425255.4.6.827.

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4

Cahill, P. A. "The GreenScreen(R) genotoxicity assay: a screening validation programme." Mutagenesis 19, no. 2 (2004): 105–19. http://dx.doi.org/10.1093/mutage/geh015.

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5

Et.al, Nur Fariza Alia Hamzah. "Chroma Key Enhance Students’ Verbal Participation During Form One English Language Lesson." Turkish Journal of Computer and Mathematics Education (TURCOMAT) 12, no. 3 (2021): 905–11. http://dx.doi.org/10.17762/turcomat.v12i3.820.

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Technology in the ESL classrooms is not something new.Using Chroma Key helps in making lesson more interactive, enjoyable and interesting.With the combination of physical and virtual technology, Chroma Keyorfrequently known as GreenScreen,creates a platformformeaningful learning. This study reveals how the use of Chroma Keyempowersa class of Form One, lower secondary school students to accomplish tasks and provides a comfortable environment to enhance students’ verbal participationsduring ESL lesson in Malaysia.
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6

Knight, Andrew W., Louise Birrell, and Richard M. Walmsley. "Development and Validation of a Higher Throughput Screening Approach to Genotoxicity Testing Using the GADD45a-GFP GreenScreen HC Assay." Journal of Biomolecular Screening 14, no. 1 (2008): 16–30. http://dx.doi.org/10.1177/1087057108327065.

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There is a pressing need to develop rapid yet accurate screening assays for the identification of genotoxic liability and for early hazard assessment in drug discovery. The GADD45a-GFP human cell-based genotoxicity assay (GreenScreen HC) has been reformatted to test 12 compounds per 96-well microplate in a higher throughput, automated screening mode and the protocol applied to the analysis of 1266 diverse, pharmacologically active compounds. Testing from a fixed starting concentration of 100 µM and over 3 serial dilutions, the hit rates for genotoxicity (7.3%) and cytotoxicity (33%) endpoints of the assay have been determined in a much wider chemical space than previously reported. The degree of interference from color, autofluorescence, and low solubility has also been assessed. The assay results have been compared to an in silico approach to genotoxicity assessment using Derek for Windows software. Where carcinogenicity data were available, GreenScreen HC demonstrated a higher specificity than in silico methods while identifying genotoxic species that were not highlighted for genotoxic liability in structure-activity relationship software. Higher throughput screening from a fixed, low concentration reduces sensitivity to less potent genotoxins, but the maintenance of the previously reported high specificity is essential in early hazard assessment where misclassification can lead to the needless rejection of potentially useful compounds in drug development. ( Journal of Biomolecular Screening 2009:16-30)
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7

Pyun, Da Hee, Young Woon Kim, Yong Woo Hwang, Seong You Lee, and Soon Ho Park. "A Hazard Assessment of Chemicals in Liquid Synthetic Detergent Using GreenScreen." Korean Journal of Hazardous Materials 9, no. 1 (2021): 30–40. http://dx.doi.org/10.31333/kihm.2021.9.1.30.

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8

Johnson, Donna, and Richard Walmsley. "Histone-deacetylase inhibitors produce positive results in the GADD45a-GFP GreenScreen HC assay." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 751, no. 2 (2013): 96–100. http://dx.doi.org/10.1016/j.mrgentox.2012.12.009.

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9

Hastwell, Paul W., Thomas W. Webster, Matthew Tate, et al. "Analysis of 75 marketed pharmaceuticals using the GADD45a-GFP ‘GreenScreen HC’ genotoxicity assay." Mutagenesis 24, no. 5 (2009): 455–63. http://dx.doi.org/10.1093/mutage/gep029.

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10

Van Gompel, J., F. Woestenborghs, D. Beerens, et al. "An assessment of the utility of the yeast GreenScreen assay in pharmaceutical screening." Mutagenesis 20, no. 6 (2005): 449–54. http://dx.doi.org/10.1093/mutage/gei062.

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