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Four overlapping ecological regions have been identified on the Table Rocks, with considerable differences in the variety of wildlife found in each.
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Although at first sight the fold change threshold may seem to be low, we could confirm all changes in gene expression identified on the microarray (Table 2).
There were 40 probes corresponding to 31 prohormone genes, including three probes corresponding to the duplicated GH genes and SST2 identified on the array (Table 3).
There are five other knob-into-holes cases easily identified on the interaction network (Table 4).
MGA_0195 and MGA_0793 were identified on the protein level (Table 2).
Using a stringent false discovery rate (FDR = 0.05), 513 CUX1 binding sites were identified on the ENCODE array (Table 1).
Two additional muscle proteins, the heavy chain(s) of muscle myosin (e.g. MHC-1) and a paramyosin (PMY), were identified on the 2D gels (Table 1).
Only 1/18 patients had ≥3 species isolated (Staphylococcus epidermitis, Staphylococcus warneri, Streptococcus mitis), 6/18 patients had 2 species and 11/18 patients had 1 species identified on the conjunctival swab (Table 2).
The species of all but 1 midge abdomen could be molecularly identified on the basis of ITS1 (Table 2).
Further, some major components of the hemicellulolytic system of T. reesei, such as β-xylosidase (BXL1), xylanase (XYN), xyloglucanase (Cel74A) and arabinofuranosidase (ABFI), were also identified on the 2-D gels (Table 2).
Few significant group differences were identified on the measures of FA (Tables 2 and 3).
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