Results 151 to 160 of about 65,972 (187)

Divergent roles of red cell arginase in humans and mice: RBC Arg1 KO mice show preserved systemic l-arginine bioavailability and infarct size in vivo. [PDF]

Redox Biol
Heuser SK, Li J, Li Z, LoBue A, Heard K, Hocks J, Suvorava T, Cadeddu RP, Strupp C, Dunaway L, Zhuge Z, Gelhaus SL, Heinen A, Germing U, Feelisch M, Carlström M, Isakson B, Kelm M, Lundberg JO, Cortese-Krott MM.   +19 more
europepmc   +1 more source

Correction: A role of arginase-1-expressing myeloid cells in cachexia. [PDF]

Cancer Metab
Lamsal A, Andersen SB, Nonstad U, Kurganovs NJ, Skipworth RJ, Bjørkøy G, Pettersen K.   +6 more
europepmc   +1 more source

Arginase in Asthma

The Open Nitric Oxide Journal, 2010
North, Michelle L., Meurs, Hermanus, Zaagsma, Johan, Scott, Jeremy, A., Maarsingh, Harm   +4 more
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The human arginases and arginase deficiency

Journal of Inherited Metabolic Disease, 1998
AbstractArginase is the final enzyme in the urea cycle. Its deficiency is the least frequently described disorder of this cycle. It results primarily in elevated blood arginine, and less frequently in either persistent or acute elevations in blood ammonia.
R, Iyer, C P, Jenkinson, J G, Vockley, R M, Kern, W W, Grody, S, Cederbaum   +5 more
openaire   +2 more sources

Arginase deficiency

The Indian Journal of Pediatrics, 1997
Hyperargininemia due to arginase deficiency is a rare, inherited, urea cycle disorder. We report a case of arginase deficiency in a 5-year old boy presenting with mild hyperammonemia, hyperargininemia, and dibasic aminoaciduria.
R, Christopher, V, Rajivnath, K T, Shetty   +2 more
openaire   +2 more sources

Arginase-1 deficiency

Journal of Molecular Medicine, 2015
Arginase-1 (ARG1) deficiency is a rare autosomal recessive disorder that affects the liver-based urea cycle, leading to impaired ureagenesis. This genetic disorder is caused by 40+ mutations found fairly uniformly spread throughout the ARG1 gene, resulting in partial or complete loss of enzyme function, which catalyzes the hydrolysis of arginine to ...
Yuan Yan, Sin, Garrett, Baron, Andreas, Schulze, Colin D, Funk   +3 more
openaire   +2 more sources

Human platelet arginase

Molecular and Cellular Biochemistry, 1980
We report here, for the first time the presence of arginase in human platelets. This enzyme has been partially purified and some of it properties studied. Its biological significance and its involvement in polyamine biosynthesis are considered.
V R, Villanueva, M, Giret
openaire   +2 more sources

Arginase

British Journal of Pharmacology, 2009
Allergic asthma is a chronic inflammatory airways' disease, characterized by allergen-induced early and late bronchial obstructive reactions, airway hyperresponsiveness (AHR), airway inflammation and airway remodelling. Recent ex vivo and in vivo studies in animal models and asthmatic patients have indicated that arginase may play a central role in all
Maarsingh, Harm, Zaagsma, Johan, Meurs, Herman   +2 more
openaire   +1 more source

Arginase in Glomerulonephritis

Nephron Experimental Nephrology, 2000
Arginase metabolizes <i>L</i>-arginine to <i>L</i>-ornithine and urea. Two arginase isoforms, AI (liver arginase) and AII (ubiquitously expressed, functions unknown), have been identified. It is clear that arginases potentially have important roles in addition to urea generation for high concentrations are present at ...
S N, Waddington, V, Cattell
openaire   +2 more sources