Hereditary disorders of the urea cycle in man: Biochemical and molecular approaches
- 1 January 1987
- book chapter
- Published by Springer Nature
- Vol. 108, 21-68
- https://doi.org/10.1007/bfb0034071
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Amplification of human argininosuccinate synthetase pseudogenesJournal of Molecular Biology, 1986
- Cloning and expression in Escherichia coli of cDNA for arginase of rat liverBiochemical and Biophysical Research Communications, 1986
- The precursor to ornithine carbamyl transferase is transported to mitochondria as a 5S complex containing an import factorBiochemical and Biophysical Research Communications, 1985
- Regulation of mRNA levels of rat liver carbamoylphosphate synthetase by glucocorticosteroids and cyclic AMP as estimated with a specific cDNABiochemical and Biophysical Research Communications, 1984
- Increased tryptophan uptake into the brain in hyperammonemiaLife Sciences, 1983
- Effect of propionate and pyruvate on citrulline synthesis and ATP content in rat liver mitochondriaBiochemical and Biophysical Research Communications, 1979
- Argininemia treated from birthThe Journal of Pediatrics, 1979
- ArgininemiaThe Journal of Pediatrics, 1977
- Citrullinemia: Investigation and treatment over afour-year periodThe Journal of Pediatrics, 1974
- Enzymatic synthesis of acetylglutamate by mammalian liver preparations and its stimulation by arginineBiochemical and Biophysical Research Communications, 1971