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Journal Abstract Search

118 related items for PubMed ID: 1718439

  • 21. 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; 27(3):304-10. PubMed ID: 2181395
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  • 22. 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; 151(1):103-12. PubMed ID: 1560037
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  • 23. 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; 4(12):1351-9. PubMed ID: 7909460
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  • 24. 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
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  • 25. 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
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  • 26. Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts.
    Santos MJ, Ojeda JM, Garrido J, Leighton F.
    Proc Natl Acad Sci U S A; 1985 Oct 15; 82(19):6556-60. PubMed ID: 2995971
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  • 27. Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.
    Stanczak H, Kremser K, Singh AK, Ashcraft J, Stanley W, Singh I.
    Hum Hered; 1992 Oct 15; 42(3):172-8. PubMed ID: 1511996
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  • 28. Identification of a catalase-negative sub-population of peroxisomes induced in mouse liver by clofibrate.
    Klucis E, Crane DI, Hughes JL, Poulos A, Masters CJ.
    Biochim Biophys Acta; 1991 Jul 08; 1074(2):294-301. PubMed ID: 1676600
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  • 30. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr 08; 122(4):573-9. PubMed ID: 8463903
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  • 32. Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.
    Wanders RJ, Kos M, Roest B, Meijer AJ, Schrakamp G, Heymans HS, Tegelaers WH, van den Bosch H, Schutgens RB, Tager JM.
    Biochem Biophys Res Commun; 1984 Sep 28; 123(3):1054-61. PubMed ID: 6148939
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  • 36. 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 28; 88(5):491-9. PubMed ID: 1372585
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  • 38. Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
    Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T.
    Pediatr Res; 1996 May 28; 39(5):812-5. PubMed ID: 8726233
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  • 39. Peroxisomal disorders. A review of a recently recognized group of clinical entities.
    Talwar D, Swaiman KF.
    Clin Pediatr (Phila); 1987 Oct 28; 26(10):497-504. PubMed ID: 2443295
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