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Literature summary for 3.5.3.1 extracted from

  • Grasemann, H.; Schwiertz, R.; Matthiesen, S.; Racke, K.; Ratjen, F.
    Increased arginase activity in cystic fibrosis airways (2005), Am. J. Respir. Crit. Care Med., 172, 1523-1528.
    View publication on PubMed

Application

Application Comment Organism
medicine patients with cystic fibrosis, before and after 14 days of antibiotic treatment for pulmonary exacerbation. Systemic enzyme levles are significantly increased in cystic fibrosis with exacerbation. Enzyme levels normalize with antibiotic treatment. Plasma L-arginine is reduced before, but not after treatment, L-ornithine, L-proline, and L-glutamic acid are normal before and increased after treatment Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
patients with cystic fibrosis, before and after 14 days of antibiotic treatment for pulmonary exacerbation
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