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194 related items for PubMed ID: 2697558

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patients.
    Heikoop JC, van den Berg M, Strijland A, Weijers PJ, Just WW, Meijer AJ, Tager JM.
    Eur J Cell Biol; 1992 Apr; 57(2):165-71. PubMed ID: 1511694
    [Abstract] [Full Text] [Related]

  • 3. Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.
    Heikoop JC, Van den Berg M, Strijland A, Weijers PJ, Schutgens RB, Just WW, Wanders RJ, Tager JM.
    Biochim Biophys Acta; 1991 Jul 26; 1097(1):62-70. PubMed ID: 1677591
    [Abstract] [Full Text] [Related]

  • 4. 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 Jul 26; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 5. 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 26; 151(1):103-12. PubMed ID: 1560037
    [Abstract] [Full Text] [Related]

  • 6. 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 26; 29(2):141-6. PubMed ID: 1673025
    [Abstract] [Full Text] [Related]

  • 7. Major peroxisomal membrane polypeptides are synthesized in cultured skin fibroblasts from patients with Zellweger syndrome.
    Suzuki Y, Shimozawa N, Orii T, Hashimoto T.
    Pediatr Res; 1989 Aug 26; 26(2):150-3. PubMed ID: 2771521
    [Abstract] [Full Text] [Related]

  • 8. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.
    Nguyen T, Bjorkman J, Paton BC, Crane DI.
    J Cell Sci; 2006 Feb 15; 119(Pt 4):636-45. PubMed ID: 16449325
    [Abstract] [Full Text] [Related]

  • 9. Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.
    Espeel M, Roels F, Giros M, Mandel H, Peltier A, Poggi F, Poll-The BT, Smeitink JA, Van Maldergem L, Santos MJ.
    Eur J Cell Biol; 1995 Aug 15; 67(4):319-27. PubMed ID: 8521871
    [Abstract] [Full Text] [Related]

  • 10. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
    Zoeller RA, Allen LA, Santos MJ, Lazarow PB, Hashimoto T, Tartakoff AM, Raetz CR.
    J Biol Chem; 1989 Dec 25; 264(36):21872-8. PubMed ID: 2689450
    [Abstract] [Full Text] [Related]

  • 11. Biogenesis of peroxisomes in fetal liver.
    Espeel M, Depreter M, Nardacci R, D'Herde K, Kerckaert I, Stefanini S, Roels F.
    Microsc Res Tech; 1997 Dec 01; 39(5):453-66. PubMed ID: 9408912
    [Abstract] [Full Text] [Related]

  • 12. Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly.
    Santos MJ, Imanaka T, Shio H, Small GM, Lazarow PB.
    Science; 1988 Mar 25; 239(4847):1536-8. PubMed ID: 3281254
    [Abstract] [Full Text] [Related]

  • 13. Peroxisomal integral membrane proteins in control and Zellweger fibroblasts.
    Santos MJ, Imanaka T, Shio H, Lazarow PB.
    J Biol Chem; 1988 Jul 25; 263(21):10502-9. PubMed ID: 3292528
    [Abstract] [Full Text] [Related]

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  • 16. OCTN3 is a mammalian peroxisomal membrane carnitine transporter.
    Lamhonwah AM, Ackerley CA, Tilups A, Edwards VD, Wanders RJ, Tein I.
    Biochem Biophys Res Commun; 2005 Dec 30; 338(4):1966-72. PubMed ID: 16288981
    [Abstract] [Full Text] [Related]

  • 17. 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 30; 27(3):304-10. PubMed ID: 2181395
    [Abstract] [Full Text] [Related]

  • 18. Peroxisome mosaicism in the livers of peroxisomal deficiency patients.
    Espeel M, Mandel H, Poggi F, Smeitink JA, Wanders RJ, Kerckaert I, Schutgens RB, Saudubray JM, Poll-The BT, Roels F.
    Hepatology; 1995 Aug 30; 22(2):497-504. PubMed ID: 7635418
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  • 20. Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7.
    Santos MJ, Moser AB, Drwinga H, Moser HW, Lazarow PB.
    Pediatr Res; 1993 May 30; 33(5):441-4. PubMed ID: 8511016
    [Abstract] [Full Text] [Related]

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