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The design of novel small molecules for studying the interaction with DNA is one of the most important goals in modern medicinal chemistry.
Mitochondrial DNA (mtDNA) is one of the most widely used molecules for studying diverse evolutionary processes.
One potential benefit of using small molecules for studying biological processes is the possibility of obtaining leads for further drug development efforts.
This suggests that a useful bound of the copy number of newly synthesized molecules for studying the lambda switch network system could be in the order of 150 200 copies under reasonable initial conditions.
The paper by Fenstermacher, Rall, Patlak and Levin [ 6] is primarily about the application of the ventriculocisternal perfusion method and it further established that sucrose and inulin were good ECS molecules for studying diffusion in the ECS.
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The array of functionalities in the product stereoselectively obtained by the cascade reaction is useful for further structural modifications directed toward the total synthesis of fusidane and other triterpenes, and designed molecules intended for studying structure activity relationships.
Taken together, our results provide a molecule basis for studying pigs, which are excellent animal models for studying teeth development and regeneration.
31– 38 EPUFAs are expected to be useful molecules for studies of ocular health and disease, including DEDs and POAG.
Alanine dipeptide (Ace-Ala-Nme) is a small molecule widely used for studying biomolecular motion, as it is simple and exhibits an extensive range of torsional angles.
The ability to modulate function specifically and rapidly makes small molecules especially useful tools for studying processes like development in which the timing of protein function is critical.
Thus, the rational designed RhoA subfamily-specific small molecule inhibitor is useful for studying the physiological and pathologic roles of Rho GTPase.
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