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(C ) Experiment 2, 'color-swap' experiment: Mybl2 -specific shRNA M3 coupled with GFP (right) or RFP (left) expression associated with a significant expansion of Mybl2 -downregulated cells (p=0.007 and p=0.001, respectively).
Left: Expression of a GAL4-inducible shRNA transgene against GFP (UAS-GFP-RNAi) will result in gene knockdown by degrading mRNA of fusion protein; Right: GFP fusion proteins can be targeted for ubiquitination-mediated degradation by a modified ubiquitination system called deGradFP (UAS-NSlmbvhhGFP4 ).
While RIP1-Tag2; RIP1-VEGFB mice presented with a similar number of tumors as RIP1-Tag2 mice (Figure 2c, left), expression of the VEGF-B transgene unexpectedly resulted in a significant reduction in total tumor burden by 39% (Figure 2c, right; 59.0±8.2 mm3 vs 35.7±4.2 mm3; p<0.05).
Acid-regulated, PacC dependent (left); expression gated by PacC at both pH 4 and pH 8 (right).
Principal axis 1, which retained 75.6% of the total variability, sorts genes according their fold change in over (on the right) and under (on the left) expression conditions independently of the stress condition applied.
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Virus replication is blocked at a late stage of morphogenesis in mammalian cells, leaving expression of late, as well as early, viral genes unimpaired [29].
In the maize leaves, expression of the At4/IPS1-like RNA showed a very strong negative correlation to phosphate concentration of the leaves under all tested stress conditions.
Consequently, we used teashirt-GAL80 (tsh-GAL80; Clyne and Miesenböck, 2008) to suppress thoracic expression, but leaving expression in the descending interneurons.
(middle), Suppressing Gal4-dependent expression in F cells (ppk23-Gal4, UAS-CD8::tdTomato, vGlut-LexA, lexAop-Gal80 ) leaves expression intact in M cells.
(right), Suppressing LexA-dependent expression in F cells (ppk23-LexA, lexAop-CD2 GFP, lexAop-CD2 GFP-Gal80 ) leaves expression intact in M cells.
Subsequently, EBV establishes a lifelong persistent infection of memory B cells, a process accompanied by epigenetic silencing of most viral coding genes, but leaving expression of non-coding small RNAs unaffected (Thorley-Lawson and Allday, 2008; Paschos et al., 2009).
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