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All E. coli isolates were genotyped to determine multilocus sequence typing group; examples of each group were characterized for additional relevant resistance mechanisms.
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Twenty-eight cultivars were characterized for partial resistance (Additional File 2).
A functional role for p53 in the serum starvation-mediated CDDP sensitization was investigated by comparing p53 deficient (p53−/−) versus p53 proficient (p53+/+) Hcells cells [ 17] (functionally characterized for response to CDDP in Additional file 1: Figure S2).
Also, two additional peaks were characterized for the oxidation of Mo5+ to Mo6+ and V4+ to V5+ at 3.5 and 4 V, respectively.
White and black colonies were identified on L-DOPA medium with neomycin and the isolates were characterized for capsule formation and cell morphology (Additional file 6).
For each morph, the SSU gene was characterized from at least one pool of cells and one individual cell, and in most cases genes were also characterized from additional pools and single cells (Table 1).
Insertion sites were characterized for their distribution throughout the genome and proximity to genes (Additional file 2: Dataset S1).
The tumors have been characterized for clinical and pathological features (data are summarized in Table S1 in Additional file 1).
As tumor subsets become better characterized, the need for additional prevention studies can be anticipated to address larger subsets (e.g. a combination of drugs for overlap) versus smaller subsets of individuals at risk.
Candidate targets that were positive in both assays with at least one siRNA were further characterized using additional siRNAs for the same target gene, so as to eliminate false positive identification caused by siRNA off-target artifacts.
Of these, the products of 57 of the genes have been previously characterized (See Additional file 17 for references).
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