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Previous work has shown that drugs which reverse the expression of disease associated genes have potential to be efficacious for treating the disease in question.
The giant (biggest) network component contains 97.4% (298/306) of the total nodes, suggesting that most of the genes have potential relationships that contribute to tumorigenesis.
A total of 322 genes have potential NsrR binding sites within 70 base pairs of DNA upstream of their translational start codons, including both the hmpA1 and hmpA2 genes (Fig. 1B).
Furthermore, many inflammatory response-related genes have potential xenobiotic-responsive elements (XREs) embedded in upstream sequences.
Some of these genes have potential functional connections to neurological disorders.
It is believe that these genes have potential to be methylated aberrantly in cancers.
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PMEPA1, along with other highly androgen-induced prostate-specific genes, has potential to serve as an androgen signaling read-out biomarker in prostate tissue.
Among these, 54 genes had potential mutations in both siblings.
Eliminating the expression of these genes has potential therapeutic utility for breast cancer.
This region contains several important genes having potential use as biomarkers for NPC detection.
Although it would be necessary to perform functional analysis to identify genes having potential functions in the mechanism described above, several candidate genes could be identified by gene microarray analysis.
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CEO of Professional Science Editing for Scientists @ prosciediting.com