These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
22. Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities. Sogawa H; Oyanagi K; Nakao T Pediatr Res; 1977 Sep; 11(9 Pt 1):949-53. PubMed ID: 904980 [No Abstract] [Full Text] [Related]
23. Hyperargininemia, epilepsy and the metabolism of guanidino compounds. Wiechert P; Marescau B; De Deyn PP; Lowenthal A Padiatr Grenzgeb; 1989; 28(2):101-6. PubMed ID: 2657590 [TBL] [Abstract][Full Text] [Related]
24. Hyperargininemia: the rat as a model for the human disease and the comparative response to enzyme replacement therapy with free arginase and arginase-loaded erythrocytes in vivo. Adriaenssens K; Karcher D; Marescau B; Van Broeckhoven C; Lowenthal A; Terheggen HC Int J Biochem; 1984; 16(7):779-86. PubMed ID: 6468738 [TBL] [Abstract][Full Text] [Related]
25. Properties of arginase from liver of Macaca fascicularis; comparison of normals with red blood cell arginase deficient monkeys. Terasaki K; Spector EB; Hendrickson R; Cederbaum SD Biochem Genet; 1980 Oct; 18(9-10):829-41. PubMed ID: 7225081 [TBL] [Abstract][Full Text] [Related]
26. Arginase deficiency in multiple tissues in argininemia. Michels VV; Beaudet AL Clin Genet; 1978 Jan; 13(1):61-7. PubMed ID: 624188 [TBL] [Abstract][Full Text] [Related]
27. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971 [No Abstract] [Full Text] [Related]
28. Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme. Grody WW; Kern RM; Klein D; Dodson AE; Wissman PB; Barsky SH; Cederbaum SD Hum Genet; 1993 Mar; 91(1):1-5. PubMed ID: 8454280 [TBL] [Abstract][Full Text] [Related]
29. Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis. Korman SH; Gutman A; Stemmer E; Kay BS; Ben-Neriah Z; Zeigler M Prenat Diagn; 2004 Nov; 24(11):857-60. PubMed ID: 15565656 [TBL] [Abstract][Full Text] [Related]
30. Arginase and free amino acids in hyperargininemia: leukocyte arginine as a diagnostic parameter for heterozygotes. Marescau B; Pintens J; Lowenthal A; Terheggen HG; Adriaenssens K J Clin Chem Clin Biochem; 1979 Apr; 17(4):211-7. PubMed ID: 438730 [TBL] [Abstract][Full Text] [Related]
31. Molecular genetic study of human arginase deficiency. Grody WW; Klein D; Dodson AE; Kern RM; Wissmann PB; Goodman BK; Bassand P; Marescau B; Kang SS; Leonard JV Am J Hum Genet; 1992 Jun; 50(6):1281-90. PubMed ID: 1598908 [TBL] [Abstract][Full Text] [Related]
32. Human salivary arginase and its deficiency in argininaemia. Konarska L; Tomaszewski L; Colombo JP; Terheggen HG J Clin Chem Clin Biochem; 1985 Jun; 23(6):337-42. PubMed ID: 4020330 [TBL] [Abstract][Full Text] [Related]
33. Roles of conserved residues in the arginase family. Perozich J; Hempel J; Morris SM Biochim Biophys Acta; 1998 Jan; 1382(1):23-37. PubMed ID: 9507056 [TBL] [Abstract][Full Text] [Related]
34. Chemical modification and inactivation of rat liver arginase by N-bromosuccinimide: reaction with His141. Daghigh F; Cavalli RC; Soprano DR; Ash DE Arch Biochem Biophys; 1996 Mar; 327(1):107-12. PubMed ID: 8615679 [TBL] [Abstract][Full Text] [Related]
35. Isoenzyme pattern and immunological properties of arginase in normal and hyperargininemia fibroblasts. Konarska L; Wiesmann U; von Fellenberg R; Colombo JP Enzyme; 1983; 29(1):44-53. PubMed ID: 6404622 [TBL] [Abstract][Full Text] [Related]
37. The activity of Plasmodium falciparum arginase is mediated by a novel inter-monomer salt-bridge between Glu295-Arg404. Wells GA; Müller IB; Wrenger C; Louw AI FEBS J; 2009 Jul; 276(13):3517-30. PubMed ID: 19456858 [TBL] [Abstract][Full Text] [Related]
38. Generation of a mouse model for arginase II deficiency by targeted disruption of the arginase II gene. Shi O; Morris SM; Zoghbi H; Porter CW; O'Brien WE Mol Cell Biol; 2001 Feb; 21(3):811-3. PubMed ID: 11154268 [TBL] [Abstract][Full Text] [Related]
39. A novel mutation in ARG1 gene is responsible for arginase deficiency in an Asian family. Hertecant JL; Al-Gazali LI; Karuvantevida NS; Ali BR Saudi Med J; 2009 Dec; 30(12):1601-3. PubMed ID: 19936428 [TBL] [Abstract][Full Text] [Related]