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Most of the enzymes used in the work described here are well-characterized and commercially available (described in Table 2), and data from CPH substrates was in good agreement with previous findings.
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The characteristics of the SEARCH breast cancer study participants for whom genotyping and vital status data were available are described in Table 1.
To address the possibility that methodological differences across studies may have influenced these results, we pooled all available data described in Table 2 and estimated the GRRs as before (Farrington et al, 2005).
Arrays ranging in size from 1.5 to 30 m were constructed depending on the available space, as described in Table 1.
The next step in testing such a tool is to apply it to individual patient data [ 20, 43] across nationally representative samples (e.g., the publicly available data sources described in Table 1) and determine its specificity and sensitivity to NH admission over various follow-up intervals, thus offering empirical evidence for its efficacy as a screening tool for risk of NH entry.
A subset of these patients had more detailed report forms available (n=66) and are described in Table 2. Definitions and categorization of donor recipient HLA-matching and conditioning regimens were assigned according to published CIBMTR criteria.
All projects used in the evaluations are available in their respective repositories, described in Table 4.
We ran an additional model by adding a protective variable (farm clothes and boots available for professional visitors), as described in Table 5, in the farm-based and combined multilevel models.
For noise suppression related impairments, a total of 192 speech signals (half English half French) are available, covering 24 degradation conditions as described in Table 2. Table 2 Description of the 24 available noise suppression related degradation conditions.
Breast cancer slices from seven patients (six samples cultured in the absence (control) or presence of 1,25(OH)2D3 100nM and one sample cultured in the presence of 1,25(OH)2D3 0.5nM) were available for analysis (from the patients described in Table 1).
The remaining 40 sequences described in Table 1 are available in GenBank (KT724890-KT724929).
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