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A 2011 CDC study that evaluated several different Campylobacter stool antigen assays concluded, however, that the performance of stool antigen assays was insufficient as a sole diagnostic for Campylobacter spp (12 ).
Recently a review of immunohistochemical (IHC) ER and PR assays concluded that luminal cancers should be candidates for endocrine therapies if at least 1% of malignant cells are immunoreactive [ 3].
Kremer et al., in an extensive interlaboratory study comparing nine PCR-based assays, concluded that MIRU-VNTR and FLiP methods are both rapid, highly reliable, and discriminative epidemiological typing tools for M. tuberculosis [ 18].
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In vitro assays conclude that there is no significant (p < 0.05) level of cytotoxicity and genotoxicity at the tested concentrations (250 2000 μg/ml) in peripheral blood mononuclear cells.
Additional studies of the influence of the aminoterminal and internal peptide sequence, carried out using the peptide transport assay, concluded that these positions have little effect on TAP affinity, with the exception of Pro residues in several positions which decreased transport efficiency [34] [36].
Deduction from the MIC and FIC index evaluations coupled with results from the kinetic growth assay concluded that components in F-10 act synergistically with ampicillin in inhibiting MRSA's growth.
With in vitro binding and DYNLL1 knockdown assays, we concluded that DYNLL1-BCL2L11-BECN1 forms a complex and that DYNLL1 facilitates the BCL2L11-BECN1 interaction.
Because the results showed the same trends observed in direct binding assays, we concluded that this competitive binding assay represents a useful assay for high-throughput screening for EH domain inhibitors.
Consistent with the running start primer extension assays, we concluded that in the presence of all four human Y-family polymerases, hPolη catalyzed the majority of nucleotide incorporation events, including opposite the lesion site.
In statistical Raman assays, we conclude from downshifted 2D- and G-modes for SWCNTs, as well as upshifted 2D- and downshifted G-modes for NG, that these electronic interactions result in stable n-doping of SWCNTs and NG.
Based on the structure of this complex, together with homology modeling based on other nAChR subtypes and binding affinity assays, we conclude that Asp-11 of LvIA plays an important role in the selectivity of LvIA towards α3β2 and α3/α6β2β3 nAChRs by making a salt bridge with Lys-155 of the rat α3 subunit.
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