BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 6442743)

  • 1. Biochemical heterogeneity of ornithine carbamoyl transferase(OCT) in patients with OCT deficiency.
    Matsuda I; Nagata N; Ohyanagi K; Tsuchiyama A; Yamamoto H; Hase Y; Kodama H; Kai Y
    Jinrui Idengaku Zasshi; 1984 Sep; 29(3):327-33. PubMed ID: 6442743
    [No Abstract]   [Full Text] [Related]  

  • 2. Some kinetic properites of liver ornithine carbamoyl transferase (OCT) in a patient with OCT deficiency.
    van der Heiden C; Desplanque J; Bakker HD
    Clin Chim Acta; 1977 Nov; 80(3):519-27. PubMed ID: 21051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Arginine 109 to glutamine mutation in a girl with ornithine carbamoyl transferase deficiency.
    Strautnieks S; Rutland P; Malcolm S
    J Med Genet; 1991 Dec; 28(12):871-4. PubMed ID: 1757964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Ornithine transcarbamylase deficiencies in human males. Kinetic and immunochemical classification.
    Briand P; Francois B; Rabier D; Cathelineau L
    Biochim Biophys Acta; 1982 May; 704(1):100-6. PubMed ID: 7093283
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Toward a molecular understanding of ornithine transcarbamylase deficiency.
    Fox JE; Rosenberg LE
    Adv Neurol; 1988; 48():71-81. PubMed ID: 2891259
    [No Abstract]   [Full Text] [Related]  

  • 7. Immunochemical study of ornithine transcarbamylase deficiency.
    Kodama H; Nagayama H; Shimoizumi H; Okabe I; Kamoshita S
    J Inherit Metab Dis; 1984; 7(3):131-2. PubMed ID: 6438397
    [No Abstract]   [Full Text] [Related]  

  • 8. The ornithine transcarbamylase gene: new "private" mutations in four patients and study of a polymorphism.
    Tuchman M; Plante RJ; Giguère Y; Lemieux B
    Hum Mutat; 1994; 3(3):318-20. PubMed ID: 8019569
    [No Abstract]   [Full Text] [Related]  

  • 9. Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency.
    Matsuura T; Hoshide R; Komaki S; Kiwaki K; Endo F; Nakamura S; Jitosho T; Matsuda I
    J Inherit Metab Dis; 1995; 18(3):273-82. PubMed ID: 7474892
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.
    Tuchman M
    J Lab Clin Med; 1992 Dec; 120(6):836-50. PubMed ID: 1453106
    [No Abstract]   [Full Text] [Related]  

  • 11. Immunochemical analysis of carbamyl phosphate synthetase I and ornithine transcarbamylase deficient livers: elevated N-acetylglutamate level in a liver lacking carbamyl phosphate synthetase protein.
    Zhang W; Holzknecht RA; Butkowski RJ; Tuchman M
    Clin Invest Med; 1990 Aug; 13(4):183-8. PubMed ID: 2208834
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene symbol: OTC. Disease: ornithine carbamoyltransferase deficiency.
    Hwu WL; Huang YT; Chien YH; Yeh HY; Lu F; Chou SP; Lin JM; Chiang SC
    Hum Genet; 2003 Sep; 113(4):367. PubMed ID: 12974280
    [No Abstract]   [Full Text] [Related]  

  • 13. The sparse fur mouse as a model for gene therapy in ornithine carbamoyltransferase deficiency.
    Batshaw ML; Yudkoff M; McLaughlin BA; Gorry E; Anegawa NJ; Smith IA; Hyman SL; Robinson MB
    Gene Ther; 1995 Dec; 2(10):743-9. PubMed ID: 8750014
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simultaneous detection of mutant gene and transgene in ornithine carbamoyl-transferase-deficient spf-ash mice with rat OCT gene.
    Kobayashi K; Horiuchi M; Yokokouji A; Shimada T; Saheki T
    J Inherit Metab Dis; 1992; 15(5):792-6. PubMed ID: 1434519
    [No Abstract]   [Full Text] [Related]  

  • 15. [On the behavior of ornithine carbamoyl-transferase (OCT) in myocardial infarct].
    Lorentz K
    Verh Dtsch Ges Inn Med; 1967; 73():761-3. PubMed ID: 5591834
    [No Abstract]   [Full Text] [Related]  

  • 16. Ultrastructural, immunocytochemical and stereological investigation of hepatocytes in a patient with the mutation of the ornithine transcarbamylase gene.
    Zimmer KP; Matsuda I; Matsuura T; Mori M; Colombo JP; Fahimi HD; Koch HG; Ullrich K; Harms E
    Eur J Cell Biol; 1995 May; 67(1):73-83. PubMed ID: 7641731
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutation affecting a splice site in exon 4 of the ornithine carbamoyl transferase gene.
    Strautnieks S; Malcolm S
    Hum Mol Genet; 1993 Nov; 2(11):1963-4. PubMed ID: 8281162
    [No Abstract]   [Full Text] [Related]  

  • 18. Seven new mutations in the human ornithine transcarbamylase gene.
    Tuchman M; Plante RJ; McCann MT; Qureshi AA
    Hum Mutat; 1994; 4(1):57-60. PubMed ID: 7951259
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probe.
    Pembrey ME; Old JM; Leonard JV; Rodeck CH; Warren R; Davies KE
    J Med Genet; 1985 Dec; 22(6):462-5. PubMed ID: 3001312
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypocitrullinemia in expanded newborn screening by LC-MS/MS is not a reliable marker for ornithine transcarbamylase deficiency.
    Cavicchi C; Malvagia S; la Marca G; Gasperini S; Donati MA; Zammarchi E; Guerrini R; Morrone A; Pasquini E
    J Pharm Biomed Anal; 2009 Jul; 49(5):1292-5. PubMed ID: 19359120
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.