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197 related items for PubMed ID: 2689450

  • 1. 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]

  • 2. Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
    Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Fujiki Y.
    J Clin Invest; 1992 Nov 25; 90(5):1864-70. PubMed ID: 1430210
    [Abstract] [Full Text] [Related]

  • 3. Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.
    Tsukamoto T, Yokota S, Fujiki Y.
    J Cell Biol; 1990 Mar 25; 110(3):651-60. PubMed ID: 1689731
    [Abstract] [Full Text] [Related]

  • 4. Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.
    Kinoshita N, Ghaedi K, Shimozawa N, Wanders RJ, Matsuzono Y, Imanaka T, Okumoto K, Suzuki Y, Kondo N, Fujiki Y.
    J Biol Chem; 1998 Sep 11; 273(37):24122-30. PubMed ID: 9727033
    [Abstract] [Full Text] [Related]

  • 5. Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly.
    Zoeller RA, Raetz CR.
    Proc Natl Acad Sci U S A; 1986 Jul 11; 83(14):5170-4. PubMed ID: 3460088
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  • 8. 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 11; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 9. Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.
    Kanzawa N, Shimozawa N, Wanders RJ, Ikeda K, Murakami Y, Waterham HR, Mukai S, Fujita M, Maeda Y, Taguchi R, Fujiki Y, Kinoshita T.
    J Lipid Res; 2012 Apr 11; 53(4):653-63. PubMed ID: 22253471
    [Abstract] [Full Text] [Related]

  • 10. [Human peroxisome-deficient disorders and pathogenic gene].
    Fujiki Y.
    Rinsho Shinkeigaku; 1994 Dec 11; 34(12):1219-21. PubMed ID: 7539728
    [Abstract] [Full Text] [Related]

  • 11. Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.
    Zoeller RA, Rangaswamy S, Herscovitz H, Rizzo WB, Hajra AK, Das AK, Moser HW, Moser A, Lazarow PB, Santos MJ.
    J Biol Chem; 1992 Apr 25; 267(12):8299-306. PubMed ID: 1569085
    [Abstract] [Full Text] [Related]

  • 12. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
    Abe Y, Honsho M, Nakanishi H, Taguchi R, Fujiki Y.
    Biochim Biophys Acta; 2014 Apr 04; 1841(4):610-9. PubMed ID: 24418004
    [Abstract] [Full Text] [Related]

  • 13. 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 04; 50(2):407-17. PubMed ID: 2697558
    [Abstract] [Full Text] [Related]

  • 14. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
    Muntau AC, Mayerhofer PU, Paton BC, Kammerer S, Roscher AA.
    Am J Hum Genet; 2000 Oct 04; 67(4):967-75. PubMed ID: 10958759
    [Abstract] [Full Text] [Related]

  • 15. Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.
    Okumoto K, Bogaki A, Tateishi K, Tsukamoto T, Osumi T, Shimozawa N, Suzuki Y, Orii T, Fujiki Y.
    Exp Cell Res; 1997 May 25; 233(1):11-20. PubMed ID: 9184070
    [Abstract] [Full Text] [Related]

  • 16. Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.
    Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Kondo N, Kinoshita N, Fujiki Y, Tsukamoto T, Osumi T, Imanaka T, Orii T, Beemer F, Mooijer P, Dekker C, Wanders RJ.
    Am J Hum Genet; 1998 Dec 25; 63(6):1898-903. PubMed ID: 9837841
    [No Abstract] [Full Text] [Related]

  • 17. Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.
    Ghaedi K, Itagaki A, Toyama R, Tamura S, Matsumura T, Kawai A, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y.
    Exp Cell Res; 1999 May 01; 248(2):482-8. PubMed ID: 10222139
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 33(5):441-4. PubMed ID: 8511016
    [Abstract] [Full Text] [Related]

  • 19. 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 May 01; 42(3):172-8. PubMed ID: 1511996
    [Abstract] [Full Text] [Related]

  • 20. Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.
    Stevens VL, Raetz CR.
    J Biol Chem; 1990 Sep 15; 265(26):15653-8. PubMed ID: 1975590
    [Abstract] [Full Text] [Related]

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