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We found that versican 3'UTR is targeted by multiple miRNAs, which have common targets such as Rb1 and PTEN.
While it has yet to be determined whether inflammatory and stress signaling pathways are proximal or distal to organelle dysfunction or triggered by peptide or lipid mediators, it is evident that many of these harmful responses have common targets in regulating insulin receptor signaling.
miRNAs 221 and 222 are two highly homologous microRNAs that have common targets [ 1, 2].
We note that the miRNAs involved in each rule may have common targets.
Despite the fact that PKA and Sch9 are distinct in Maf1 regulation and probably many other biological processes, they have common targets [ 41].
The Pka1 and TOR pathways mainly control cellular responses to glucose and nitrogen, respectively, and are known to have common targets.
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Calvo et al. have reported that NUP98-HOXA9 enforce strong transcription of endogenous Hoxa9 and Hoxa7, which further strengthen that different NUP98-Hox fusions have common target genes.
These antibiotics have different structures, but they all have common target site, the bacterial ribosome.
The oncogenic pathways regulated by beta-catenin, Src, ERBB2, and Ras overlap and have common target genes.
Using this approach, we classified several interactions of samples that displayed partial overlap with two or more other samples that did not necessarily have common target genes.
These expression patterns suggest that different estrogens have common target tissues (e.g., liver, heart, muscle, otic vesicle), but they have different degrees of effect on the different tissues (i.e., tissue-specific responsiveness), with different potential health effect outcomes.
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