Your English writing platform
Discover LudwigExact(10)
Most frequently, we observed a defect in muscles 6 and 7 whereby instead of running parallel, the two crossed, each appearing to insert improperly at the insertion site of the other (Figure 6B).
Using these cells, we observed a defect in PDGF-BB-induced Akt phosphorylation on Ser473, but also on Thr308.
We also observed a defect in the monoubiquitin conjugation to PTEN-SUMO1 complexes using in vitro assays.
However, we and others have now observed a defect in cohesin loading in the absence of Chl1 (Laha et al. 2011).
In accordance with these results, we observed a defect in FANCD2 foci formation in USP1-depleted human cells (Fig. 4B and C).
Previously, we surveyed the H3K9me2 distribution via immunolabeling of Argonaute single mutant males and observed a defect only in csr-1 mutants (She et al. 2009).
Similar(50)
We did observe a defect in juvenile-to-adult phase transition in the cao/ch1 mutant under our growth conditions.
Therefore, amongst the maternal RNAs (representative of the various transport pathways) examined to date, we only observe a defect in maternal sqt RNA localization.
For example, we found that Lsd1 deletion with VavCre or Mx1Cre resulted in severe HSC differentiation and self-renewal defects resulting in complete loss of lineage-negative c-Kit+ myeloid progenitor cells, whereas Sprüssel et al. (2012) did not observe a defect in LT-HSCs.
Similarly we observed a small defect in CD1d expression in dnRas DP thymocytes.
Strikingly, we observed a strong defect in capsule production, where strain 1F8 generates little capsule visible by India ink staining (Figure 5A).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com