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123 related items for PubMed ID: 1586963

  • 1. 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; 17(1):1-8. PubMed ID: 1586963
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 Jun 03; 14(2):152-64. PubMed ID: 1679469
    [Abstract] [Full Text] [Related]

  • 4. [Neuropathology of peroxisomal disorders; Zellweger syndrome and neonatal adrenoleukodystrophy].
    Takashima S, Houdou S, Kamei J, Hasegawa M, Mito T, Suzuki Y, Maeda K.
    No To Hattatsu; 1992 Mar 03; 24(2):186-93. PubMed ID: 1567656
    [Abstract] [Full Text] [Related]

  • 5. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.
    Singh I, Voigt RG, Sheikh FG, Kremser K, Brown FR.
    Biochem Mol Med; 1997 Aug 03; 61(2):198-207. PubMed ID: 9259985
    [Abstract] [Full Text] [Related]

  • 6. Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.
    Balfe A, Hoefler G, Chen WW, Watkins PA.
    Pediatr Res; 1990 Mar 03; 27(3):304-10. PubMed ID: 2181395
    [Abstract] [Full Text] [Related]

  • 7. Three peroxisome protein packaging pathways suggested by selective permeabilization of yeast mutants defective in peroxisome biogenesis.
    Zhang JW, Luckey C, Lazarow PB.
    Mol Biol Cell; 1993 Dec 03; 4(12):1351-9. PubMed ID: 7909460
    [Abstract] [Full Text] [Related]

  • 8. 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 03; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 9. FRET microscopy demonstrates molecular association of non-specific lipid transfer protein (nsL-TP) with fatty acid oxidation enzymes in peroxisomes.
    Wouters FS, Bastiaens PI, Wirtz KW, Jovin TM.
    EMBO J; 1998 Dec 15; 17(24):7179-89. PubMed ID: 9857175
    [Abstract] [Full Text] [Related]

  • 10. Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy.
    Small GM, Santos MJ, Imanaka T, Poulos A, Danks DM, Moser HW, Lazarow PB.
    J Inherit Metab Dis; 1988 Dec 15; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 11. The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein.
    Gärtner J, Chen WW, Kelley RI, Mihalik SJ, Moser HW.
    Pediatr Res; 1991 Feb 15; 29(2):141-6. PubMed ID: 1673025
    [Abstract] [Full Text] [Related]

  • 12. Nonspecific lipid transfer protein (sterol carrier protein-2) defective in patients with deficient peroxisomes.
    Suzuki Y, Yamaguchi S, Orii T, Tsuneoka M, Tashiro Y.
    Cell Struct Funct; 1990 Oct 15; 15(5):301-8. PubMed ID: 2085845
    [Abstract] [Full Text] [Related]

  • 13. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr 15; 122(4):573-9. PubMed ID: 8463903
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.
    Wiemer EA, Brul S, Just WW, Van Driel R, Brouwer-Kelder E, Van Den Berg M, Weijers PJ, Schutgens RB, Van Den Bosch H, Schram A.
    Eur J Cell Biol; 1989 Dec 21; 50(2):407-17. PubMed ID: 2697558
    [Abstract] [Full Text] [Related]

  • 16. Low-density particles (W-particles) containing catalase in Zellweger syndrome and normal fibroblasts.
    Aikawa J, Chen WW, Kelley RI, Tada K, Moser HW, Chen GL.
    Proc Natl Acad Sci U S A; 1991 Nov 15; 88(22):10084-8. PubMed ID: 1946426
    [Abstract] [Full Text] [Related]

  • 17. Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidase.
    Christensen E, Woldseth B, Hagve TA, Poll-The BT, Wanders RJ, Sprecher H, Stokke O, Christophersen BO.
    Scand J Clin Lab Invest Suppl; 1993 Nov 15; 215():61-74. PubMed ID: 8327852
    [Abstract] [Full Text] [Related]

  • 18. Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
    Shimozawa N, Zhang Z, Suzuki Y, Imamura A, Tsukamoto T, Osumi T, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N.
    Biochem Biophys Res Commun; 1999 Aug 27; 262(2):504-8. PubMed ID: 10462504
    [Abstract] [Full Text] [Related]

  • 19. 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 27; 84(5):1425-8. PubMed ID: 3469675
    [Abstract] [Full Text] [Related]

  • 20. Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
    Schram AW, Strijland A, Hashimoto T, Wanders RJ, Schutgens RB, van den Bosch H, Tager JM.
    Proc Natl Acad Sci U S A; 1986 Aug 27; 83(16):6156-8. PubMed ID: 2426710
    [Abstract] [Full Text] [Related]

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