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Inhibition of XPO1 by SINE compounds is expected to enhance nuclear localization for proteins that rely upon XPO1 for nuclear export.
In contrast to S0 state, the excited-state intramolecular proton transfer (ESIPT) process at S1 state in these compounds is expected to be approximately less barrier height.
Eventually, a cocktail of direct-acting compounds is expected to eliminate the need for IFN entirely.
The mass size of our compounds is expected to be 569 and 573 for isoprostanes and the internal standard, respectively.
Consequently, patient exposure to a wide spectrum of volatile species (hydrocarbons, aldehydes, ketones, aromatics, heterocyclic compounds) is expected during hemodialysis.
Many hydrocarbons are, however, toxic to microorganisms and endogenous biosynthesis of these compounds is expected to have adverse effects on cell growth and production yield [ 7].
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REE polishing compounds are expected to see large increase in use as well.
Because of this reason, antioxidant compounds are expected to play potential beneficial role in this disease.
These compounds are expected to be used as prototype for further development of selective anti-cancer drug candidate.
These compounds are expected to be used as precursors for designing new crosslinked molecular imprinting membranes (MIMs), exhibiting high stability of the template memory.
Organic cathode materials that involve conducting polymers, organic carbonyl/sulfur compounds are expected to be promising candidates for future LIBs with a concept of "green and sustainable".
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com