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Before the analysis, we confirmed that there were no differences in the total bacterial numbers tested (adhesive cells and non-adhesive cells) in the cultured bacteria among various concentration of S-PRG eluate (Fig. 5A,B).
From the analysis, we confirmed that this thick membrane structure achieved three times higher sensitivity compared to the conventional design by decreasing 70%% of the mass of the thick membrane part with keeping the resonance frequency same.
Before using the imputed constituent levels in the analysis, we confirmed that the Bayesian spatial GP modeling was appropriate for imputation via a cross-validation (CV) study (see Supplemental Material, "Cross validation study").
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On the whole, with the correlation analysis, we confirmed the clinical relevance of the S-estimator maps.
Nevertheless, in the sensitivity analysis, we confirmed the robustness of the overall estimate by including only panel studies.
Subsequent to the bioinformatic analysis, we confirmed that the regulation of Dhc93AB indeed mirrors that of nan and iav.
Given that TB enters dead cells and may interfere with the fluorescent analysis, we confirmed high cell viability (96%).
In the combined analysis, we confirmed association between rs765250 and SBP; carriers of rs765250 [A] were associated with an overall increase in SBP, with a mean effect on natural log transformed SBP of +0.01, [95%CI:0.02], 0.02], p = 2×10−4, equivalent to ∼2.0 mmHg.
In agreement with the microarray analysis, we confirmed that crabp1 mRNA and protein levels were highly expressed in ASC-Ls.
In the present immunohistochemical analysis, we confirmed the intratumoral expression of BCD after the direct administration of the adenoviral vector into tumour xenografts.
Based on the Western blot analysis, we confirmed that combination of F-10 with ampicillin (both at sub-inhibitory concentration) totally suppressed the expression of PBP2a in MRSA.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com