The human arginases and arginase deficiency

Journal of Inherited Metabolic Disease

Volumn 21, Issue SUPPL. 1, 1998, Pages 86-100

  Iyer, R ^a   Jenkinson, C P ^a   Vockley, J G ^b   Kern, R M ^a   Grody, W W ^a   Cederbaum, S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b GLAXOSMITHKLINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; ARGINASE; BENZOIC ACID; KIDNEY ENZYME; LIVER ENZYME; NITRIC OXIDE; ORNITHINE; PHENYLACETIC ACID; POLYAMINE;

AMINO ACID SEQUENCE; AMMONIA BLOOD LEVEL; AMPHIBIA; BIOSYNTHESIS; CONFERENCE PAPER; CONTROLLED STUDY; DIET THERAPY; ENZYME DEFICIENCY; EVOLUTION; GENETIC CONSERVATION; HUMAN; POLYAMINE METABOLISM; UREA CYCLE;

AMINO ACID METABOLISM, INBORN ERRORS; AMINO ACID SEQUENCE; ANIMALS; ARGINASE; ARGININE; CELL LINE; HUMANS; ISOENZYMES; MOLECULAR SEQUENCE DATA;

EID: 0031903783     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1005313809037     Document Type: Article

References (7)

1. Ash DE, Scolnick LR, Kanyo ZF, Vockley JG, Cederbaum SD, Christianson DW (1998) Molecular basis of argininemia: structure-function consequences of mutations in human liver arginase. Mol Genet Metab, in press.
2. Brusilow SW, Horwich AL (1995) Urea cycle enzymes. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Diseases, 7th edn. New York: McGraw-Hill, 621-663.
3. G-hydroxyarginine during high-output nitric oxide production. Am J Physiol 271 : H1988-H1998.
4. Cederbaum SD, Moedjono SJ, Shaw KNF, Naylor EW, Walser M, Carter M (1982) Treatment of hyperargininaemia due to arginase deficiency. J Inter Metab Dis 5: 95-99.
5. Cederbaum SD, Shaw KNF, Spector EB, Verity MA, Snodgrass PJ, Sugarman GI (1979) Hyperargininemia due to arginase deficiency. Pediatr Res 13: 827-833.
6. Cerone R, Coruso U, Barabino A et al (1997) Hyperargininemia: pre-natal diagnosis and treatment from birth. In De Deyn PP, Marescau B, Qureshi IA, Mori A, eds. Guanidino Compounds in Biology and Medicine II. London: John Libbey, 71-75.
7. De Deyn PP, Marescau B, Qureshi IA et al (1997) Hyperargininemia: a treatable inborn error of metabolism. In De Deyn PP, Marescau B, Qureshi IA, Mori A. eds. Guanidino Compounds in Biology and Medicine II. London: John Libbey, 53-69.