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Journal Abstract Search

118 related items for PubMed ID: 1718439

  • 1. Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group.
    Wiemer EA, Out M, Schelen A, Wanders RJ, Schutgens RB, Van den Bosch H, Tager JM.
    Biochim Biophys Acta; 1991 Oct 21; 1097(3):232-7. PubMed ID: 1718439
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  • 2. 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 Oct 21; 14(2):152-64. PubMed ID: 1679469
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  • 10. Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.
    Heikoop JC, Van den Berg M, Strijland A, Weijers PJ, Schutgens RB, Just WW, Wanders RJ, Tager JM.
    Biochim Biophys Acta; 1991 Jul 26; 1097(1):62-70. PubMed ID: 1677591
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  • 13. 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 26; 34(3):270-6. PubMed ID: 7510868
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  • 14. Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly.
    Suzuki Y, Shimozawa N, Yajima S, Orii T, Yokota S, Tashiro Y, Osumi T, Hashimoto T.
    Cell Struct Funct; 1992 Feb 26; 17(1):1-8. PubMed ID: 1586963
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  • 15. Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.
    Wanders RJ, Heymans HS, Schutgens RB, Poll-Thé BT, Saudubray JM, Tager JM, Schrakamp G, van den Bosch H.
    J Neurol Sci; 1988 Apr 26; 84(2-3):147-55. PubMed ID: 2454298
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  • 16. Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins.
    Wanders RJ, Schutgens RB, Schrakamp G, van den Bosch H, Tager JM, Schram AW, Hashimoto T, Poll-Thé BT, Saudubrau JM.
    Eur J Pediatr; 1986 Aug 26; 145(3):172-5. PubMed ID: 2429839
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  • 17. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
    Zoeller RA, Allen LA, Santos MJ, Lazarow PB, Hashimoto T, Tartakoff AM, Raetz CR.
    J Biol Chem; 1989 Dec 25; 264(36):21872-8. PubMed ID: 2689450
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  • 19. Resistance to erucic acid as a selectable marker for peroxisomal activity: isolation of revertants of an infantile Refsum disease cell line.
    Bachir Bioukar E, Straehli F, Ng KH, Rolland MO, Hashimoto T, Carreau JP, Deschatrette J.
    J Inherit Metab Dis; 1994 Dec 25; 17(1):41-59. PubMed ID: 7519689
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  • 20. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar 25; 24(2):194-7. PubMed ID: 1373633
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