BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (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
    [TBL] [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; 1083(3):305-9. PubMed ID: 2049396
    [TBL] [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; 14(2):152-64. PubMed ID: 1679469
    [TBL] [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; 24(2):186-93. PubMed ID: 1567656
    [TBL] [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; 61(2):198-207. PubMed ID: 9259985
    [TBL] [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; 27(3):304-10. PubMed ID: 2181395
    [TBL] [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; 4(12):1351-9. PubMed ID: 7909460
    [TBL] [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; 34(3):270-6. PubMed ID: 7510868
    [TBL] [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; 17(24):7179-89. PubMed ID: 9857175
    [TBL] [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; 11(4):358-71. PubMed ID: 2468817
    [TBL] [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; 29(2):141-6. PubMed ID: 1673025
    [TBL] [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(5):301-8. PubMed ID: 2085845
    [TBL] [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; 122(4):573-9. PubMed ID: 8463903
    [TBL] [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; 1097(3):232-7. PubMed ID: 1718439
    [TBL] [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; 50(2):407-17. PubMed ID: 2697558
    [TBL] [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; 88(22):10084-8. PubMed ID: 1946426
    [TBL] [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; 215():61-74. PubMed ID: 8327852
    [TBL] [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; 262(2):504-8. PubMed ID: 10462504
    [TBL] [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; 84(5):1425-8. PubMed ID: 3469675
    [TBL] [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; 83(16):6156-8. PubMed ID: 2426710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.