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 *

121 related articles for article (PubMed ID: 5812490)

  • 1. Ornithine-ketoacid aminotransferase in human liver with reference to patients with hyperornithinaemia and familial protein intolerance.
    Kekomäki MP; Räihä NC; Bickel H
    Clin Chim Acta; 1969 Jan; 23(1):203-8. PubMed ID: 5812490
    [No Abstract]   [Full Text] [Related]  

  • 2. Studies on the development of ornithine-ketoacid aminotransferase activity in mammalian liver.
    Räihä NC; Kekomäki M
    Z Klin Chem Klin Biochem; 1969 Mar; 7(2):207. PubMed ID: 5390661
    [No Abstract]   [Full Text] [Related]  

  • 3. Ornithine-ketoacid transaminase activity in human skin and amniotic fluid cell culture.
    Shih VE; Schulman JD
    Clin Chim Acta; 1970 Jan; 27(1):73-5. PubMed ID: 5412614
    [No Abstract]   [Full Text] [Related]  

  • 4. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.
    Sunshine P; Lindenbaum JE; Levy HL; Freeman JM
    Pediatrics; 1972 Jul; 50(1):100-11. PubMed ID: 5038084
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. Heterogenous mutations of the structural gene of human ornithine carbamyltransferase as observed in five personal cases.
    Cathelineau L; Saudubray JM; Polonovski C
    Enzyme; 1974; 18(1):103-13. PubMed ID: 4852265
    [No Abstract]   [Full Text] [Related]  

  • 7. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
    Matsuda I; Arashima S; Nambu H; Takekoshi Y; Anakura M
    Pediatrics; 1971 Oct; 48(4):595-600. PubMed ID: 5114747
    [No Abstract]   [Full Text] [Related]  

  • 8. [Hereditary enzyme defects of the urea cycle].
    Colombo JP
    Ergeb Inn Med Kinderheilkd; 1971; 31():97-130. PubMed ID: 4933544
    [No Abstract]   [Full Text] [Related]  

  • 9. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    Shih VE; Efron ML; Moser HW
    Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534
    [No Abstract]   [Full Text] [Related]  

  • 10. The implications of hyperammonemia in rare and common disorders, including migraine.
    Russell A
    Mt Sinai J Med; 1973; 40(5):609-30. PubMed ID: 4542418
    [No Abstract]   [Full Text] [Related]  

  • 11. Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity.
    Staudt M; Wermuth B; Freisinger P; Hässler A; Pontz BF
    J Inherit Metab Dis; 1998 Feb; 21(1):71-2. PubMed ID: 9501271
    [No Abstract]   [Full Text] [Related]  

  • 12. Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia.
    Hommes FA; Ho CK; Roesel RA; Coryell ME; Gordon BA
    J Inherit Metab Dis; 1982; 5(1):41-7. PubMed ID: 6820413
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked transmission of structural gene mutations responsible for ornithine-transcarbamylase deficiencies.
    Cathelineau L; Navarro J; Polonovski C; Saudubray JM
    Lancet; 1973 Feb; 1(7797):261-2. PubMed ID: 4119401
    [No Abstract]   [Full Text] [Related]  

  • 14. Immunochemical assay in 16 boys with ornithine transcarbamylase deficiency.
    Francois B; Briand P; Cathelineau L
    Adv Exp Med Biol; 1982; 153():53-62. PubMed ID: 6819766
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Enzymes of urea synthesis in familial protein intolerance with deficient transport of basic amino acids.
    Kekomäki M; Räihä NC; Perheentupa J
    Acta Paediatr Scand; 1967 Nov; 56(6):631-6. PubMed ID: 6077000
    [No Abstract]   [Full Text] [Related]  

  • 17. Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.
    Levin B; Abraham JM; Oberholzer VG; Burgess EA
    Arch Dis Child; 1969 Apr; 44(234):152-61. PubMed ID: 5779426
    [No Abstract]   [Full Text] [Related]  

  • 18. Regulation of arginine and ornithine metabolism at the enzymic level in rat liver and kidney.
    Civen M; Brown CB; Trimmer BM
    Arch Biochem Biophys; 1967 May; 120(2):352-8. PubMed ID: 6033452
    [No Abstract]   [Full Text] [Related]  

  • 19. Ornithine transcarbamylase, an isoelectric point (pI) isozyme in human liver and its deficiency.
    Arashima S; Matsuda I
    Biochem Biophys Res Commun; 1971 Oct; 45(1):145-50. PubMed ID: 5139917
    [No Abstract]   [Full Text] [Related]  

  • 20. Ornithine carbamyl transferase: the effects of pH on the kinetics of a mutant human enzyme.
    Cathelineau L; Saudubray JM; Polonovski C
    Clin Chim Acta; 1972 Oct; 41():305-12. PubMed ID: 4645239
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.