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Combined, these data suggest that cyclin D1 expression and localisation may influence proliferation and diagnostic factors in prostate cancer.
To search for potential targets of miR-125b that may influence proliferation, migration ability of cells, TargetScan, Pictar-Vert, and Microrna.Org were employed for this purpose.
In order to investigate potential mechanisms by which the tumor microenvironment might contribute to cancer phenotype, we asked whether soluble paracrine factors produced by stromal and neoplastic cells in vitro may influence proliferation, and gene and protein expression.
In addition, using rapid subtraction hybridization and proteomic analysis, we identified gene products generated by stromal and neoplastic cells that may influence proliferation, differentiation and apoptosis, or drive response to stimulus.
The majority of β-gal-positive cells reside in the base of the intestinal crypt, suggesting that Wnt signaling may influence proliferation in the progenitor population and not the TA-cell population.
Aiming to investigate potential mechanisms by which the tumor microenvironment might contribute to a cancer phenotype, we evaluated soluble paracrine factors produced by stromal and neoplastic cells which may influence proliferation and gene and protein expression.
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However, the OTUs from Ruminococcus microbial genus were shown to be more abundant at lower lactate concentration and with almost no abundance at higher BLC, indicating that exercise training may also influence proliferation in this genus.
The purpose of this study was to investigate whether GDF-5 may influence the proliferation, differentiation, and collagen turnover of human dental pulp cells.
These results show the effects of the graphene-based nanotopographies on the wettability of the naturally hydrophobic graphene, which may influence the proliferation of cells as a result of the adhesion of important biomolecules [20, 21, 22, 51, 52].
Taken together, these data provide a potential mechanism by which loss of Sox2 may influence cell proliferation.
In the present study, we observed that Sox2, like Sox17, bound to Smad3 and inhibited its activity, providing a potential mechanism by which Sox2 may influence cell proliferation and differentiation.
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may influence innovation
may induce proliferation
may change proliferation
may prevent proliferation
may influence adsorption
may drive proliferation
may promote proliferation
may mediate proliferation
may limit proliferation
may regulate proliferation
may inhibit proliferation
may influence preparedness
may enhance proliferation
may involve proliferation
may counteract proliferation
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