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Journal Abstract Search

118 related items for PubMed ID: 2678891

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  • 4. 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
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  • 9. Abnormalities of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of patients with Reye's syndrome.
    Sinatra F, Yoshida T, Applebaum M, Masion Hoogenraad NJ, Sunshine P.
    Pediatr Res; 1975 Nov; 9(11):829-33. PubMed ID: 171618
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  • 10. Reduced activity of otc in the liver of a patient with Reye's syndrome.
    Arashima S, Takekoshi Y, Anakura M, Nanbu H, Matsuda I.
    Adv Exp Med Biol; 1982 Nov; 153():163-70. PubMed ID: 7164895
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  • 12. Ornithine carbamoyltransferase deficiency in an adult male patient: significance of hepatic ultrastructure in clinical diagnosis.
    Tallan HH, Schaffner F, Taffet SL, Schneidman K, Gaull GE.
    Pediatrics; 1983 Feb; 71(2):224-32. PubMed ID: 6823424
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  • 14. Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency.
    Zimmer KP, Bendiks M, Mori M, Kominami E, Robinson MB, Ye X, Wilson JM.
    Mol Med; 1999 Apr; 5(4):244-53. PubMed ID: 10448647
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  • 16. Study of enzyme defect in a case of ornithine transcarbamylase deficiency.
    Qureshi IA, Letarte J, Quellet R.
    Diabete Metab; 1978 Dec; 4(4):239-41. PubMed ID: 729890
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  • 17. Human ornithine transcarbamylase. Purification and characterization of the enzyme from normal liver and the liver of a Reye's syndrome patient.
    Pierson DL, Cox SL, Gilbert BE.
    J Biol Chem; 1977 Sep 25; 252(18):6464-9. PubMed ID: 893420
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  • 18. Impact of enzyme activity assay on indication in liver transplantation for ornithine transcarbamylase deficiency.
    Wakiya T, Sanada Y, Urahashi T, Ihara Y, Yamada N, Okada N, Ushijima K, Otomo S, Sakamoto K, Murayama K, Takayanagi M, Hakamada K, Yasuda Y, Mizuta K.
    Mol Genet Metab; 2012 Mar 25; 105(3):404-7. PubMed ID: 22264779
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  • 19. Ornithine transcarbamylase deficiency: a case with a truncated enzyme precursor and a case with undetectable mRNA activity.
    Kodama H, Ohtake A, Mori M, Okabe I, Tatibana M, Kamoshita S.
    J Inherit Metab Dis; 1986 Mar 25; 9(2):175-85. PubMed ID: 3091923
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  • 20. Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and in OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoter.
    Kiwaki K, Kanegae Y, Saito I, Komaki S, Nakamura K, Miyazaki JI, Endo F, Matsuda I.
    Hum Gene Ther; 1996 May 01; 7(7):821-30. PubMed ID: 8860834
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