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The screen-printing technology is a well-established and practical approach ideal for development of electrochemical point-of-care testing [ 1].
These transcription factors are ideal for development of mechanism-based drugs since Sp1 expression decreases with age [ 39- 41], and results of animal studies show that Sp1, Sp3 and Sp4 are highly expressed in tumor but not in non-tumor tissues [ 21, 23].
At first glance, developing skills in art for transfer to a domain such as science may seem circuitous, but characteristics of art make it ideal for development of critical thinking, especially through approaches formulated in the Artful Thinking Program of Project Zero (Tishman and Palmer, 2006).
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It can be developed as an ideal candidate for development of therapeutic drugs for spinal cord injury or strike.
Taken together, our data suggest that the RBD fragment encompassing spike residues 377-588 is a critical neutralizing receptor-binding fragment and an ideal candidate for development of effective MERS vaccines, and that adding non-neutralizing structures to this RBD fragment diminishes its neutralizing potential.
A robust strain exhibiting a wide range of adaptability and tolerance to the growth conditions would be an ideal candidate for development of such bioprocess.
In such a case, LMM is considered as an ideal tool for development of predictive models [22, 68] that accounts for spatial dependence of the plots within the clusters.
In particular, proteases have proven to be ideal targets for development of optical sensors for cancer.
Thus, ABCG2 is an ideal target for development of chemo-sensitizing agents for better treatment of drug resistant cancers and helping eradicate cancer stem cells.
The ideal candidate for development of a serodiagnostic tool should be an immunogenic protein that is consistently expressed by the bloodstream-form trypanosomes.
All these previous observations make ABCG2 an ideal target for development of chemo-sensitizing agents for better treatment of drug resistant cancers and suggest that inhibiting ABCG2 unlikely will cause any side effect if the inhibitor is specific to ABCG2.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com