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Table 1.

Diet composition, as fed.

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Table 2.

Growth performance parameters of pigs in either control (CON) or sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments.

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Table 2 Expand

Table 3.

Ex vivo markers of intestinal permeability and nutrient uptake of pigs in either control (CON) or sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments.

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Table 3 Expand

Table 4.

Cecal short chain fatty acid concentrations (mM/g cecal content) of pigs in either control (CON) or sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments.

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Table 4 Expand

Table 5.

Gene abundance in the ileum of pigs in either control (CON) or sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments.

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Table 5 Expand

Fig 1.

Pairwise proteome comparisons in the A) ileum, B) colon, C) longissimus muscle (LM), and D) liver of pigs in control (CON) and sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments. Proteins identified are demonstrated in relation to average ion intensity differences and P-value (statistical significance).

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Fig 2.

Biological processes of differentially abundant proteins in in the A) ileum, B) colon, C) longissimus muscle, and D) liver of pigs in sub-therapeutic chlortetracycline (sCTC; 40 ppm) compared with control (CON) treatments.

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Fig 2 Expand

Table 6.

Significantly different protein abundances in the ileum, colon, longissimus muscle, and liver of pigs in either control (CON) or sub-therapeutic chlortetracycline (sCTC; 40 ppm) treatments.

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Table 6 Expand