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Journal Abstract Search

212 related items for PubMed ID: 1372585

  • 1. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
    Yajima S, Suzuki Y, Shimozawa N, Yamaguchi S, Orii T, Fujiki Y, Osumi T, Hashimoto T, Moser HW.
    Hum Genet; 1992 Mar; 88(5):491-9. PubMed ID: 1372585
    [Abstract] [Full Text] [Related]

  • 2. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
    Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A.
    Prog Clin Biol Res; 1990 Mar; 321():545-58. PubMed ID: 2183242
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  • 3. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
    Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ.
    J Cell Sci; 1995 May; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
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  • 4. Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
    Roscher AA, Hoefler S, Hoefler G, Paschke E, Paltauf F, Moser A, Moser H.
    Pediatr Res; 1989 Jul; 26(1):67-72. PubMed ID: 2475849
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  • 5. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar; 24(2):194-7. PubMed ID: 1373633
    [Abstract] [Full Text] [Related]

  • 6. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.
    Poll-The BT, Skjeldal OH, Stokke O, Poulos A, Demaugre F, Saudubray JM.
    Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966
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  • 10. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.
    Moser AB, Rasmussen M, Naidu S, Watkins PA, McGuinness M, Hajra AK, Chen G, Raymond G, Liu A, Gordon D.
    J Pediatr; 1995 Jul; 127(1):13-22. PubMed ID: 7541833
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  • 13. [Clinical and molecular aspects of peroxisome-deficient disorders].
    Suzuki Y, Shimozawa N, Orii T.
    Nihon Rinsho; 1993 Sep; 51(9):2353-8. PubMed ID: 7692118
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  • 14. 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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  • 16. Complementation analysis of peroxisomal disorders and classical Refsum.
    Poll-The BT, Skjeldal OH, Stokke O, Demaugre F, Saudubray JM.
    Prog Clin Biol Res; 1990 Dec 25; 321():537-43. PubMed ID: 1691507
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  • 18. Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome.
    Santos MJ, Hoefler S, Moser AB, Moser HW, Lazarow PB.
    J Cell Physiol; 1992 Apr 25; 151(1):103-12. PubMed ID: 1560037
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