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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 6790859)

  • 1. The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosa.
    Matsushima A; Orii T
    J Inherit Metab Dis; 1981; 4(2):83-4. PubMed ID: 6790859
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].
    Kopieczna-Grzebieniak E; Toborek M; Tarnawski R; Jakubowska D
    Pediatr Pol; 1987 Oct; 62(10):727-32. PubMed ID: 3328149
    [No Abstract]   [Full Text] [Related]  

  • 3. The ornithine-urea cycle: biosynthesis and regulation of carbamyl phosphate synthetase I and ornithine transcarbamylase.
    Cohen PP
    Curr Top Cell Regul; 1981; 18():1-19. PubMed ID: 7023854
    [No Abstract]   [Full Text] [Related]  

  • 4. Rat liver and intestinal mucosa differ in the developmental pattern and hormonal regulation of carbamoyl-phosphate synthetase I and ornithine carbamoyl transferase gene expression.
    Ryall JC; Quantz MA; Shore GC
    Eur J Biochem; 1986 May; 156(3):453-8. PubMed ID: 3754512
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia.
    Matsuda Y; Tsuji A; Katunuma N
    Adv Exp Med Biol; 1982; 153():77-82. PubMed ID: 7164924
    [No Abstract]   [Full Text] [Related]  

  • 6. Kinetic properties of carbamoyl-phosphate synthase (ammonia) and ornithine carbamoyltransferase in permeabilized mitochondria.
    Cohen NS; Cheung CW; Sijuwade E; Raijman L
    Biochem J; 1992 Feb; 282 ( Pt 1)(Pt 1):173-80. PubMed ID: 1540132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of urea cycle enzymopathies in childhood.
    Trauner DA; Self TW
    Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461
    [No Abstract]   [Full Text] [Related]  

  • 9. A fatal variant of human ornithine carbamoyltransferase is stimulated by Mg2+.
    Woodfin BM; Davis LE; Bernard LR; Kornfeld M
    Biochem Med Metab Biol; 1986 Dec; 36(3):300-5. PubMed ID: 3801211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical method.
    Hayasaka K; Metoki K; Ishiguro S; Kato S; Chiba T; Hirooka M; Kikuchi M; Kurobane I; Narisawa K; Tada K
    Eur J Pediatr; 1987 Jul; 146(4):370-2. PubMed ID: 3308467
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].
    Murotsuki J; Uehara S; Okamura K; Yajima A; Kikuchi M; Oura T; Miyabayashi S
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Dec; 43(12):1613-6. PubMed ID: 1744457
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expression of nuclear genes encoding the urea cycle enzymes, carbamoyl-phosphate synthetase I and ornithine carbamoyl transferase, in rat liver and intestinal mucosa.
    Ryall J; Nguyen M; Bendayan M; Shore GC
    Eur J Biochem; 1985 Oct; 152(2):287-92. PubMed ID: 2865132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome.
    Brown T; Hug G; Lansky L; Bove K; Scheve A; Ryan M; Brown H; Schubert WK; Partin JC; Lloyd-Still J
    N Engl J Med; 1976 Apr; 294(16):861-7. PubMed ID: 175276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hyperammonemia].
    Arashima S
    Nihon Rinsho; 1978 May; Suppl():1352-3. PubMed ID: 691351
    [No Abstract]   [Full Text] [Related]  

  • 15. Enzymatic analysis of citrullinemia (12 cases) in Japan.
    Saheki T; Ueda A; Hosoya M; Sase M; Nakano K; Katsunuma T
    Adv Exp Med Biol; 1982; 153():63-76. PubMed ID: 7164923
    [No Abstract]   [Full Text] [Related]  

  • 16. Mitochondrial urea cycle enzymes in rats treated with sodium benzoate.
    Colombo JP; Bachmann C; Pfister U; Gradwohl M
    Biochem Biophys Res Commun; 1988 Mar; 151(2):872-7. PubMed ID: 3348818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A lethal neonatal variant of carbamoyl-phosphate synthetase deficiency in combination with an intermediate activity of L-ornithine: 2-oxoglutarate amino-transferase.
    van der Heiden C; Beemer FA; van Dijk HA; Desplanque J; Gerards LJ
    Clin Genet; 1983 May; 23(5):363-8. PubMed ID: 6851228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis, intracellular transport, and processing of the precursors for mitochondrial ornithine transcarbamylase and carbamoyl-phosphate synthetase I in isolated hepatocytes.
    Mori M; Morita T; Ikeda F; Amaya Y; Tatibana M; Cohen PP
    Proc Natl Acad Sci U S A; 1981 Oct; 78(10):6056-60. PubMed ID: 6947214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular genetics of urea cycle diseases].
    Ohtake A; Mori M
    Seikagaku; 1990 Sep; 62(9):1170-7. PubMed ID: 2258657
    [No Abstract]   [Full Text] [Related]  

  • 20. Prospective treatment of urea cycle disorders.
    Maestri NE; Hauser ER; Bartholomew D; Brusilow SW
    J Pediatr; 1991 Dec; 119(6):923-8. PubMed ID: 1720458
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.