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Journal Abstract Search

267 related items for PubMed ID: 7544797

  • 1. 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]

  • 2. 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
    [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. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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 Mar 17; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 8. Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
    Warren DS, Morrell JC, Moser HW, Valle D, Gould SJ.
    Am J Hum Genet; 1998 Aug 17; 63(2):347-59. PubMed ID: 9683594
    [Abstract] [Full Text] [Related]

  • 9. 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 17; 26(1):67-72. PubMed ID: 2475849
    [Abstract] [Full Text] [Related]

  • 10. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].
    Molzer B, Stöckler S, Bernheimer H.
    Wien Klin Wochenschr; 1992 Jul 17; 104(21):665-70. PubMed ID: 1282286
    [Abstract] [Full Text] [Related]

  • 11. Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
    Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y.
    Am J Hum Genet; 2003 Aug 17; 73(2):233-46. PubMed ID: 12851857
    [Abstract] [Full Text] [Related]

  • 12. Glyceryl ethers in peroxisomal disease.
    Poulos A, Bankier A, Beckman K, Johnson D, Robertson EF, Sharp P, Sheffield L, Singh H, Usher S, Wise G.
    Clin Genet; 1991 Jan 17; 39(1):13-25. PubMed ID: 1705185
    [Abstract] [Full Text] [Related]

  • 13. Formation of a novel arachidonic acid metabolite in peroxisomes.
    Gordon JA, Heller SK, Rhead WJ, Watkins PA, Spector AA.
    Prostaglandins Leukot Essent Fatty Acids; 1995 Jan 17; 52(2-3):77-81. PubMed ID: 7540307
    [Abstract] [Full Text] [Related]

  • 14. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
    Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H.
    J Clin Chem Clin Biochem; 1989 May 17; 27(5):309-14. PubMed ID: 2474624
    [Abstract] [Full Text] [Related]

  • 15. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar 17; 24(2):194-7. PubMed ID: 1373633
    [Abstract] [Full Text] [Related]

  • 16. 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 17; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 17. Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview.
    Purdue PE, Skoneczny M, Yang X, Zhang JW, Lazarow PB.
    Neurochem Res; 1999 Apr 17; 24(4):581-6. PubMed ID: 10227689
    [Abstract] [Full Text] [Related]

  • 18. Metabolic control of peroxisome abundance.
    Chang CC, South S, Warren D, Jones J, Moser AB, Moser HW, Gould SJ.
    J Cell Sci; 1999 May 17; 112 ( Pt 10)():1579-90. PubMed ID: 10212151
    [Abstract] [Full Text] [Related]

  • 19. Peroxisomal disorders. Neurodevelopmental and biochemical aspects.
    Brown FR, Voigt R, Singh AK, Singh I.
    Am J Dis Child; 1993 Jun 17; 147(6):617-26. PubMed ID: 7685145
    [Abstract] [Full Text] [Related]

  • 20. Differential protein import deficiencies in human peroxisome assembly disorders.
    Motley A, Hettema E, Distel B, Tabak H.
    J Cell Biol; 1994 May 17; 125(4):755-67. PubMed ID: 7910611
    [Abstract] [Full Text] [Related]

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