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Journal Abstract Search

126 related items for PubMed ID: 2899227

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  • 8. Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.
    Singh I, Moser AE, Goldfischer S, Moser HW.
    Proc Natl Acad Sci U S A; 1984 Jul; 81(13):4203-7. PubMed ID: 6588384
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  • 9. Adrenoleukodystrophy: impaired oxidation of fatty acids due to peroxisomal lignoceroyl-CoA ligase deficiency.
    Lazo O, Contreras M, Bhushan A, Stanley W, Singh I.
    Arch Biochem Biophys; 1989 May 01; 270(2):722-8. PubMed ID: 2705786
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  • 11. Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation.
    Street JM, Singh H, Poulos A.
    Biochem J; 1990 Aug 01; 269(3):671-7. PubMed ID: 2117919
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  • 13. Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts.
    Christensen E, Grønn M, Hagve TA, Kase BF, Christophersen BO.
    Biochim Biophys Acta; 1989 Mar 14; 1002(1):79-83. PubMed ID: 2538146
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  • 19. Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
    Wanders RJ, Schutgens RB, Schrakamp G, Tager JM, Van den Bosch H, Moser AB, Moser HW.
    J Neurol Sci; 1987 Feb 14; 77(2-3):331-40. PubMed ID: 3819771
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