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Both results allow us to postulate the use of neurosteroids as potentially useful molecules in neuroregeneration after brain damage induced by prenatal ethanol exposure.
The systematic studies of the interfacial phenomena performed in the symmetrical cell comprising two lithium electrodes separated by PEG LiClO4 AlBr3 electrolyte allow us to postulate different rate of SEI (solid electrolyte interface) formation and limitation of its growth in the presence of AlBr3 interface thus enhancing the effectiveness of lithium cells.
The results presented here, together with previous observations on the role exerted by galectin-3 in several infections, allow us to postulate that regulation of the Th1/Th2 balance by galectin-3 changes with the diversity of the initial responses triggered by different pathogens.
These differences seen in gene expression levels, allow us to postulate on many candidate genes for disease resistance.
Such results allow us to postulate that the efficacy of olanzapine may be due to its effect on the regulation of dopamine -DARPP32 feedback in the cAMP signalling pathway in the hippocampus, via DNA methylation.
Together, these observations allow us to postulate that the anterior limb is less responsive to FGF signaling compared to the posterior region and hints the need for an additional signal in the AND for hairy2 induction.
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Comparative proteomic analyses, using data on φKMV (Lavigne et al. 2006), allowed us to postulate that the product of gene 42 (locus lag KP-KP34p42) whish is described as a conserved hypothetical protein could be additional structural protein (Fig. 3).
The complementary structural information allowed us to postulate a detailed reaction mechanism.
The identification of the different electroreactive species and adsorbed intermediates allowed us to postulate a reaction mechanism for the transformation of AA into dehydroascorbic acid (DHA).
These results allowed us to postulate a structural explanation for the functional diversity among TRPV channels and their differential regulation by proteins and ligands.
Finally, assays of eight Bak peptide analogues on Bcl-2 allowed us to postulate that modulations at position 78 could afford peptides with a binding selectivity enhanced for Bcl-xL.
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