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Self-assembling peptides (SAPs) are molecules designed for tissue engineering.
Molecules designed for interfering with aromatase activity have existed for many years.
Self-assembling peptides are members of a new class of molecules designed for tissue engineering and protein delivery.
Starting from these scaffolds, palladium-catalyzed reactions have been performed, including by automated procedures, to prepare libraries of molecules designed for biological applications.
As such, it is plausible that the PI3k/Akt pathway may be a target for therapeutic molecules designed for the treatment of endothelial tumors.
Interference with the export of cell surface receptors can be performed through co-expression of specific affinity molecules designed for entrapment in the endoplasmic reticulum during the export process.
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Most of the PTK inhibitors are small molecules, designed to compete for, or nearby, the ATP-binding site, and are currently in phase I III clinical trials, mainly for oncological indications.
Just last week, BMS, along with eight other companies, provided 58 compounds for an NCATS pilot program called Discovering New Therapeutic Uses for Existing Molecules, designed to develop partnerships between pharmaceutical companies and the biomedical research community to advance the development of therapeutics.
Additionally, nucleic acids (RNA and DNA molecules) are designed for novel applications in biotechnology.
Most unmodified small molecules, originally designed for vacuum evaporation, can be blade coated while the solubility is above 0.5 wt.%.
Molecules naturally designed for the acquisition of essential metals can be used as a shuttle to deliver toxic metal ions to target organisms.
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