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Journal Abstract Search

215 related items for PubMed ID: 7693762

  • 1. Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.
    Wendland M, Subramani S.
    J Clin Invest; 1993 Nov; 92(5):2462-8. PubMed ID: 7693762
    [Abstract] [Full Text] [Related]

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

  • 3. Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders.
    Wiemer EA, Nuttley WM, Bertolaet BL, Li X, Francke U, Wheelock MJ, Anné UK, Johnson KR, Subramani S.
    J Cell Biol; 1995 Jul; 130(1):51-65. PubMed ID: 7790377
    [Abstract] [Full Text] [Related]

  • 4. Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal.
    Walton PA, Gould SJ, Feramisco JR, Subramani S.
    Mol Cell Biol; 1992 Feb; 12(2):531-41. PubMed ID: 1732729
    [Abstract] [Full Text] [Related]

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  • 7. 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 Feb; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family.
    McCollum D, Monosov E, Subramani S.
    J Cell Biol; 1993 May; 121(4):761-74. PubMed ID: 8098333
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 Jul; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 12. Abnormality in catalase import into peroxisomes leads to severe neurological disorder.
    Sheikh FG, Pahan K, Khan M, Barbosa E, Singh I.
    Proc Natl Acad Sci U S A; 1998 Mar 17; 95(6):2961-6. PubMed ID: 9501198
    [Abstract] [Full Text] [Related]

  • 13. 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 17; 151(1):103-12. PubMed ID: 1560037
    [Abstract] [Full Text] [Related]

  • 14. Peroxisomal disorders: clinical commentary and future prospects.
    Wilson GN, Holmes RD, Hajra AK.
    Am J Med Genet; 1988 Jul 17; 30(3):771-92. PubMed ID: 2461077
    [Abstract] [Full Text] [Related]

  • 15. Peroxisome biogenesis in Saccharomyces cerevisiae.
    Kunau WH, Hartig A.
    Antonie Van Leeuwenhoek; 1992 Aug 17; 62(1-2):63-78. PubMed ID: 1444337
    [Abstract] [Full Text] [Related]

  • 16. Quantitative analysis of peroxisomal protein import in vitro.
    Terlecky SR, Legakis JE, Hueni SE, Subramani S.
    Exp Cell Res; 2001 Feb 01; 263(1):98-106. PubMed ID: 11161709
    [Abstract] [Full Text] [Related]

  • 17. Metabolism of branched chain fatty acids in peroxisomal disorders.
    Singh H, Usher S, Johnson D, Poulos A.
    J Inherit Metab Dis; 1990 Feb 01; 13(3):387-9. PubMed ID: 1700192
    [No Abstract] [Full Text] [Related]

  • 18. [Human peroxisome-deficient disorders and pathogenic gene].
    Fujiki Y.
    Rinsho Shinkeigaku; 1994 Dec 01; 34(12):1219-21. PubMed ID: 7539728
    [Abstract] [Full Text] [Related]

  • 19. Import of stably-folded proteins into peroxisomes.
    Walton PA.
    Ann N Y Acad Sci; 1996 Dec 27; 804():76-85. PubMed ID: 8993537
    [Abstract] [Full Text] [Related]

  • 20. Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.
    Shimozawa N, Suzuki Y, Orii T, Moser A, Moser HW, Wanders RJ.
    Am J Hum Genet; 1993 Apr 27; 52(4):843-4. PubMed ID: 7681622
    [No Abstract] [Full Text] [Related]

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