Sentence examples for more efficient therapeutics from inspiring English sources

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A better understanding of the cellular and physiological signaling of FXR and its cofactors will help develop more selective modulators and the development of more efficient therapeutics for digestive system diseases.

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Understanding the mechanism of ligand-assisted GQ folding is necessary for the design of more efficient cancer therapeutics.

Moreover, QCT was used to synthesize β-glucosidase inhibitors while targeting gluconeogenesis or glucose homeostasis was suggested to be a new strategy for developing more efficient DM therapeutics [21].

Not only do these crystal structures contribute unprecedented molecular details of opioid ligand binding and specificity, but they also represent important tools for structure-based approaches to guide the discovery of safer and more efficient opioid therapeutics.

Numerous studies are concerned about the more specific and more efficient delivery of therapeutics by applying specific combinations of biocompatible and biodegradable NMs ([ 33] and reference cited).

Drug repositioning analysis is likely to become routine for every new drug and target discovered, resulting in more efficient identification of therapeutics for targeting specific molecular aberrations.

For recent examples we may conjecture more efficient transfection of nucleic acid-based therapeutics based on the modification of chitosan combined g-stearic acid micelles by cis-aconitate [ 34] or more effective targeted delivery of osthole by N-succinyl-chitosan nanoparticles coupled with low-density lipoprotein [ 22].

Therefore, detailed and accurate characterisation of PR variant expression in breast cancer could generate novel and more efficient biomarkers of disease prognosis or targets for therapeutics.

Fourth, the drug discovery process will become more efficient (and thereby less expensive) because biomarkers will help identify the most promising candidate therapeutics worthy of further development.

Therefore, the utilization of ESV as a potential pharmacological source is a more efficient and convenient choice as a valuable source for the future development of novel human therapeutics than that of GV [ 45].

Instead, NCATS will serve as "a catalytic hub" for therapeutics development across NIH in part by studying ways to make the process more efficient, Collins said.

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