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The findings of Rztetsky et al suggest that many complex phenotypes (non-Mendelian disorders including both physical and psychiatric disorders) are probably rooted in genetic variation that is significantly shared by multiple disease phenotypes.
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Interestingly, no significantly changed proteins are shared by any two groups, indicating the distinct effects of the diuretics on the urinary proteome.
A structural rather than a catalytic role of this region can be suggested on the basis of alignment of the isolated N-terminal regions of the fungal HIS4 enzymes, which revealed that the degree of sequence similarity between them is quite low and significantly less than that shared by catalytic domains (Additional file 6 and 7).
When the TFs and partners forming potential driver circuits probed in this study (with at least one significantly misregulated target gene shared by both the TF and its partner) are analyzed for mutual exclusivity of their pattern of alterations, only few of them reveal significant (See further details in Additional file 7: Table S11).
The study replicated findings from previous studies: callous-unemotional behaviour is underpinned by genes, meaning that in the instance of one twin exhibiting callous-unemotional behaviours, callous-unemotional behaviours were significantly more likely to be shared by an identical twin than a fraternal twin.
In contrast, no significantly enriched KEGG pathways were shared by the Week 8 and Week 12 placebo groups, with FDRs < 0.10 at both time points.
Significantly, this effect was also shared by other pan-HDAC-Is such as LBH589 or TSA and by class I HDAC-Is such as VPA and MS275, but not by the specific inhibitor of HDAC-6 tubacin, indicating that class I HDAC targeting is crucial for TP induction.
Four significantly up-regulated functional terms were shared by all 5 compounds (Table 6).
DAVID functional annotation clustering analysis showed significantly enriched annotation terms that are shared by both tissues include extracellular matrix (ECM), collagens, structural proteins, ECM-receptor interaction, cell communication, and peptidase activity (Table 7).
Furthermore, responses to two doses of PCV13 were significantly higher for all 12 serotypes shared by both vaccines when compared with response in subjects who received two doses of PPSV23.
The top four GO biological process categories observed between the Finnish twins and Mexicans (Table 1) were also significantly enriched among the 34 genes shared by all three sets of samples (Additional file 5).
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