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By enrichment and molecular procedures, we identified α- and β-Proteobacteria strains, classified by 16S rDNA sequences as Dechlorospirillum sp. and Dechlorosoma sp., respectively.
Using optimization procedures, we identified three new antimicrobial saKAS III inhibitors: 6c (2,4-dichloro-benzoic acid (2,3,4-trihydroxy-benzylidene -hydrazide), 6e (4-[(3-chloro-pyrazin-2,3,4-trihydroxy-benzylidene -hydrazide), and 6 (4-[(5-trifluoromethyl-pyridin-2,3,4-trihydroxy-benzylidene -hydrazide).
Starting with a narrative review of the care provided to these patients and a critical analysis of the healthcare procedures, we identified potential shortcomings and improvements and formalised a document on recommendations for optimising the clinical and therapeutic approach for acute heart failure.
Using bisulfite sequencing and methylated DNA enrichment procedures, we identified human PHD3 promoter hypermethylation in prostate, breast, melanoma and renal carcinoma cell lines.
Through the prioritization procedures, we identified 169 DEPgenes, which exhibited high chance to be associated with depression in GWA dataset (Wilcoxon rank-sum test, p = 0.00005).
Following these procedures, we identified a set of 51 572 non-overlapping eCGIs across tissues (Supplementary Material, Table S1).
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Differently from previous procedures, we identify the existing degrees of freedom in terms of control points, and our method yields parametric polynomial surfaces that can be incorporated into commercial CAD programs.
Through this procedure we identified 13 diagnostic indicators that are stated as propositions that favor reelection of the incumbent party.
For each procedure, we identified criteria related to the patient's condition (nutritional status, respiratory status, the presence of fever) and related to the procedure (such as the experience of the endoscopist and the anesthetist, the amount of physiological saline instilled, the duration of the anesthesia).
Using an original purification procedure, we identified a 20 kDa protein that is strongly expressed in chicken gizzard smooth muscle.
Following this procedure, we identified and quantified expression levels for 169 proteins in all 6 sample pools in the first experiment, and 190 proteins in the second experiment.
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