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Suggested guidelines for the diagnosis and management of urea cycle disordersEvolution of the arginase fold and functional diversityInducible arginase 1 deficiency in mice leads to hyperargininemia and altered amino acid metabolismClinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiencySCHEMA-designed variants of human Arginase I and II reveal sequence elements important to stability and catalysis.Functions of arginase isoforms in macrophage inflammatory responses: impact on cardiovascular diseases and metabolic disorders.Label-free quantitative urinary proteomics identifies the arginase pathway as a new player in congenital obstructive nephropathy.Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?Myocyte-mediated arginase expression controls hyperargininemia but not hyperammonemia in arginase-deficient mice.Arginase: a critical regulator of nitric oxide synthesis and vascular function.Hyperargininemia: a family with a novel mutation in an unexpected site.Targeting arginase-II protects mice from high-fat-diet-induced hepatic steatosis through suppression of macrophage inflammation.Arginase: the emerging therapeutic target for vascular oxidative stress and inflammation.Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts.Genetic Targeting of Arginase-II in Mouse Prevents Renal Oxidative Stress and Inflammation in Diet-Induced Obesity.Hyperargininemia due to arginase I deficiency: the original patients and their natural history, and a review of the literature.Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency.Modulation of cancer-specific immune responses by amino acid degrading enzymes.Case Report of Argininemia: The Utility of the Arginine/Ornithine Ratio for Newborn Screening (NBS).Biopsy-proven Hepatocellular Carcinoma in a 53-year-old Woman With Arginase Deficiency.Early-onset hyperargininaemia: a severe disorder?Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency.Dynamics of arginase gene evolution in metazoans.Brain MRI and magnetic resonance spectroscopy findings in patients with hyperargininemia.Argininemia as a cause of severe chronic stunting and partial growth hormone deficiency (PGHD): A case report.Liver involvement in urea cycle disorders: a review of the literature.Naringin protects viscera from ischemia/reperfusion injury by regulating the nitric oxide level in a rat model.Deficient Arginase II Expression without Alteration in Arginase I Expression Attenuated Experimental Autoimmune Encephalomyelitis in Mice.Neonatal cholestasis: an uncommon presentation of hyperargininemia.Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Hyperargininemia due to liver arginase deficiency.
@ast
Hyperargininemia due to liver arginase deficiency.
@en
type
label
Hyperargininemia due to liver arginase deficiency.
@ast
Hyperargininemia due to liver arginase deficiency.
@en
prefLabel
Hyperargininemia due to liver arginase deficiency.
@ast
Hyperargininemia due to liver arginase deficiency.
@en
P1476
Hyperargininemia due to liver arginase deficiency.
@en
P2093
Eric A Crombez
Stephen D Cederbaum
P304
P356
10.1016/J.YMGME.2004.11.004
P577
2004-12-19T00:00:00Z