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The vascular endothelial growth factor pathway may be a relevant therapeutic target in MPM.
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The fibroblast growth factor receptor (FGFR) signaling pathways may be a relevant target in MPM.
Several of these compounds elicit selective cancer cell killing in vitro and robust efficacy in vivo, suggesting that targeting 'histone lysine methylation pathways' may be a relevant, emerging cancer therapeutic strategy.
In these aspects, the AT1R pathway may be a more clinically relevant mechanism for the acute cardiovascular events associated with ambient PM demonstrated in the epidemiologic and clinical studies, especially in patients with compromised heart function.
In addition, our results strongly suggested that aberrant ERK5 signalling and NF- κB activation contributes to increased tumour cell proliferation, migration and metastasis, and that this pathway may be a potential novel, and extremely relevant therapeutic target in human CC.
Although there is mounting evidence that this may be a relevant pathway in Drosophila metamorphosis [ 5], the role of autophagy as a positive mediator of cell death is unclear and not well understood in mammalian systems.
Although the molecular mechanisms underlying this effect remain poorly understood, evidence exists supporting the notion that the regulation of RBP4 gene transcription via the cAMP signaling pathway may be physiologically relevant.
However, recent findings suggest a more direct role for dendritic cells, which opens up the possibility that a similar pathway may be relevant in the causation of conjunctival fibrosis, particularly in allergic eye disease.Conjunctival fibrosis is a serious clinical concern and is associated with chronic inflammation of the ocular surface tissue, such as in allergic eye disease.
In addition, the specific effects of daunorubicin on the glycolysis pathway may be relevant to its antitumor effect.
Accordingly, β-tubulin/tau pathway may be relevant in determining toxicity risk and response to paclitaxel treatment.
The conservation of this pathway in fish and human cells, suggests that this pathway may be relevant to target in AML pre-clincial mammalian models.
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