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Some software packages for molecular formula identification using isotope patterns are summarized in Table 1.
Weight increases of each of the circuit patterns are summarized in Table 1.
Hydroxycinnamoyl-quinic acid and hydroxycinnamoyl-isocitric acid structures are shown in Scheme 1 and the MS fragmentation patterns are summarized in Table 1.
Susceptibility patterns are summarized in Table 1 and MIC distributions for amoxicillin-clavulanate, piperacillin-tazobactam and cefoxitin are shown in Table 2.
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Clustering of isolates on the basis of matching fingerprint patterns is summarized in Table 1.
All detected metabolites, retention times, and fragmentation patterns were summarized in (Table 3).
A breakdown of all the modules grouped into the 4 patterns is summarized in Table S3-S5 (Additional file 1).
The MIC50 and MIC90 values, MIC ranges and susceptibility in % of selected isolates with different ERIC-PCR patterns were summarized in Table 1.
Identification of these protein spots and their expression patterns is summarized in Table 2 and Figure 3. Three out of the 5 spots were identified as component-3 of the proteose peptone (CPP3).
The scores for each feature, per stripe, per pattern, are summarized in Table 1.
The specific findings and individual white matter staining pattern for each case with mutations in the PRNP open reading frame, relevant clinical data, codon 129 genotype, western blotting results, and cortical PrP pattern, are summarized in Table 2 and subsequently in this paragraph.
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