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Further studies in pigs revealed that a high degree of NH2-terminal degradation of GLP-1 occured in the hepatic portal system (34), concomitant with the evidence that DPP-4 is found in high concentrations in hepatocytes and endothelial cells (35, 36)
The mapped reads were then quantified by htseq-count (version 2.0.3) [34] allowing to generate a count table by sample
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