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Filters are commonly employed to remove a large number of hazardous molecules and especially volatile organic compounds (VOC), odorous molecules or dioxins and furans present in industrial emissions.
Indeed in vitro and in vivo pharmacological investigation showed that these new molecules and especially those containing a thiocarbamate linker possess superior antioxidant properties compared with α-lipoic acid and to the amide or carbamate linker analogs.
The latter findings are exciting in the light of the possibility of more pharmacological application of these bioactive probiotic molecules, and especially cost-effective production and targeted delivery of bioactive peptides seems to emerge as a feasible strategy to harness this knowledge.
However, these molecules, and especially myo-inositol can take part in various cellular processes, and further analysis was therefore required to understand the cellular processes triggering PCD in atips1.
A protein cannot interact with DNA independently of mutual conformational changes because all interactions between biological molecules, and especially those between specifically interacting biological molecules, will alter each constituent's structure.
Since 1996, thanks to the discovery of new classes of drugs and molecules and especially with the introduction of combined therapies, the life expectancy and QoL of HIV patients have enormously improved.
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This suggests that the network structure cannot be reconciled with the non-monotone dependence of the two key signaling molecules JNK and especially NFAT with respect to the ligand concentration.
The paracellular pathway is regulated by several junctional proteins: (i) tight junctions are formed by occludins, claudins, and junctional adhesion molecules (JAM) and especially JAM-B is detected in endothelial cells; (ii) GAP junctions are formed by connexins; and (iii) adherent junctions represent homotypic adhesion between cells and are formed by vascular endothelial (VE) cadherins.
Cationic lipids have become known as one of the most versatile tools for the delivery of DNA, RNA and many other therapeutic molecules, and are especially attractive because they can be easily designed, synthesized and characterized.
A highly fluorescent metal organic framework In-MOF, In OH bpydcc (bpydc = biphenyl-5,5′-dicarboxylate)) imparting additional luminescent Eu3+ ions has been synthesized for sensing organic molecules and anions, especially chloroform and MnO4−, both of them have a significant spectral response.
An increased residence time as well as an increased binding affinity of synthetic insulin-like molecules towards IRA and especially IGF1R might affect carcinogenesis [ 2, 3].
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