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Altogether these results show that Myc overexpression is not solely responsible for the phenotypes induced by B52 overexpression in this lineage and strongly suggest that Brat, as well as other suppressors identified in the screen, antagonizes B52 effects at multiple levels.
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Since all antibodies screened that antagonize signaling in Wnt3a-stimulated HEK293 cells also inhibit Wnt3a stimulation in all other cell lines tested, and also inhibit autocrine Wnt signaling in teratocarcinoma cell lines, it was intriguing that these antibodies potentiate autocrine Wnt signaling in the other nine cell lines tested.
We speculate that the suppressors identified in our screen, including Brat, antagonize B52 effects by acting on multiple targets and/or at multiple levels.
Silencing of white+ results in flies with white eyes and this has been used successfully in a screen to find genes that antagonize the siRNA pathway (Lee and Carthew, 2003).
Here we performed a genetic screen to determine what DUB, if any, antagonizes the function of the APC/C in the fission yeast Schizosaccharomyces pombe.
We used an IFN-β promoter-driven luciferase reporter plasmid (pIFN-β-luc) to screen for individual ZIKV proteins that can antagonize IFN-β production (Supplementary Fig. 1a).
(Fairchild is far warmer than her antagonizing on-screen persona; she is also not an alcoholic or an addict like the character).
Therefore, IRFAP-HTS was utilized to screen 11,258 FDA-approved and drug-like small molecules for those that antagonize Lgr5 internalization.
While the characters insult and antagonize one another, their thoughts spool across the bottom of the screen in the form of text, like a never-ending news update.
In agreement with activation of both oncogenes, RASSF1C promoted motility and invasion and was antagonized by RASSF1A, independently of other SRC activators identified in our screen.
This model then provided the rationale for a focused chemical screen which, based on existing antiandrogen scaffolds, identified three novel compounds that effectively antagonized AR F876L (and AR WT) to suppress the growth of prostate cancer cells resistant to enzalutamide.
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