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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.
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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].
Bennett et al. (2008) demonstrated AluS activity using a plasmid-based mobilization assay but concluded that sequence decay of older AluS elements in vivo occurred more rapidly than the propagation of new copies, supporting a model for their extinction.
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.
We conclude that assays for antibodies against citrullinated antigens differ in their ability to predict poorer outcomes in patients with EPA.
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.
Because 32% of the ferret serum had a titer >20 in this assay, we concluded that these animals most likely had been exposed to a CoV.
Osimitz et al. [ 30] reported that a very dilute mixture of the three monomers that comprise part of the chemical composition of Tritan™ showed no EA in an uterotrophic assay and concluded that the manufactured resin should therefore leach no chemicals having EA.
However, at submicromolar concentrations they report that, unlike 25OHC, a structural enantiomer, 'ent-25HC', was inactive (although some activity was observed at high concentration) in an antiviral assay, and concluded that the antiviral effects of low-concentration 25OHC are mediated by specific receptor binding.
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