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105 related items for PubMed ID: 1883627

  • 1. Immunochemical analysis of the peroxisomal beta-oxidation enzymes in rat and human heart and skeletal muscle and in skeletal muscle of Zellweger patients.
    Reubsaet FA, Brückwilder ML, Veerkamp JH, Trijbels JM, Hashimoto T, Monnens LA.
    Biochem Med Metab Biol; 1991 Apr; 45(2):197-203. PubMed ID: 1883627
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  • 2. Acyl-CoA oxidase activity and peroxisomal fatty acid oxidation in rat tissues.
    Reubsaet FA, Veerkamp JH, Bukkens SG, Trijbels JM, Monnens LA.
    Biochim Biophys Acta; 1988 Feb 19; 958(3):434-42. PubMed ID: 3342250
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  • 3. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
    Reubsaet FA, Veerkamp JH, Brückwilder ML, Trijbels JM, Hashimoto T, Monnens LA.
    Biochim Biophys Acta; 1991 Jun 03; 1083(3):305-9. PubMed ID: 2049396
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  • 6. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.
    Guerroui S, Aubourg P, Chen WW, Hashimoto T, Scotto J.
    Biochem Biophys Res Commun; 1989 May 30; 161(1):242-51. PubMed ID: 2471528
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  • 7. Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
    Schram AW, Goldfischer S, van Roermund CW, Brouwer-Kelder EM, Collins J, Hashimoto T, Heymans HS, van den Bosch H, Schutgens RB, Tager JM.
    Proc Natl Acad Sci U S A; 1987 Apr 30; 84(8):2494-6. PubMed ID: 2882519
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  • 8. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr 30; 122(4):573-9. PubMed ID: 8463903
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  • 9. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.
    Suzuki Y, Shimozawa N, Orii T, Igarashi N, Kono N, Hashimoto T.
    Clin Chim Acta; 1988 Feb 29; 172(1):65-76. PubMed ID: 2452040
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  • 10. Individual peroxisomal beta-oxidation enzymes.
    Hashimoto T.
    Ann N Y Acad Sci; 1982 Feb 29; 386():5-12. PubMed ID: 6953852
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  • 11. Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.
    van Roermund CW, Brul S, Tager JM, Schutgens RB, Wanders RJ.
    J Inherit Metab Dis; 1991 Feb 29; 14(2):152-64. PubMed ID: 1679469
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  • 12. Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.
    Tager JM, Van der Beek WA, Wanders RJ, Hashimoto T, Heymans HS, Van den Bosch H, Schutgens RB, Schram AW.
    Biochem Biophys Res Commun; 1985 Feb 15; 126(3):1269-75. PubMed ID: 3977916
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  • 16. Properties of peroxisomal 3-ketoacyl-coA thiolase from rat liver.
    Miyazawa S, Furuta S, Osumi T, Hashimoto T, Ui N.
    J Biochem; 1981 Aug 15; 90(2):511-9. PubMed ID: 6117552
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  • 17. Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.
    Suzuki Y, Lee K, Shimozawa N, Orii T, Kondo N.
    Cell Struct Funct; 1997 Dec 15; 22(6):615-9. PubMed ID: 9591053
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  • 18. The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes.
    Miyazawa S, Osumi T, Hashimoto T.
    Eur J Biochem; 1980 Feb 15; 103(3):589-96. PubMed ID: 6766863
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  • 19. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I.
    Pediatr Res; 1993 Sep 15; 34(3):270-6. PubMed ID: 7510868
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  • 20. Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.
    Chen WW, Watkins PA, Osumi T, Hashimoto T, Moser HW.
    Proc Natl Acad Sci U S A; 1987 Mar 15; 84(5):1425-8. PubMed ID: 3469675
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