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Journal Abstract Search

228 related items for PubMed ID: 9382874

  • 1. Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.
    Faust PL, Hatten ME.
    J Cell Biol; 1997 Dec 01; 139(5):1293-305. PubMed ID: 9382874
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  • 2. The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction.
    Faust PL, Su HM, Moser A, Moser HW.
    J Mol Neurosci; 2001 Dec 01; 16(2-3):289-97; discussion 317-21. PubMed ID: 11478384
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  • 3. Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.
    Maxwell M, Bjorkman J, Nguyen T, Sharp P, Finnie J, Paterson C, Tonks I, Paton BC, Kay GF, Crane DI.
    Mol Cell Biol; 2003 Aug 01; 23(16):5947-57. PubMed ID: 12897163
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  • 4. Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.
    Gärtner J, Brosius U, Obie C, Watkins PA, Valle D.
    Eur J Cell Biol; 1998 Aug 01; 76(4):237-45. PubMed ID: 9765053
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  • 5. Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.
    Kovacs WJ, Shackelford JE, Tape KN, Richards MJ, Faust PL, Fliesler SJ, Krisans SK.
    Mol Cell Biol; 2004 Jan 01; 24(1):1-13. PubMed ID: 14673138
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  • 8. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.
    Faust PL, Banka D, Siriratsivawong R, Ng VG, Wikander TM.
    J Inherit Metab Dis; 2005 Jan 01; 28(3):369-83. PubMed ID: 15868469
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  • 11. A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
    Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Shirayoshi Y, Mori T, Fujiki Y.
    Science; 1992 Feb 28; 255(5048):1132-4. PubMed ID: 1546315
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  • 12. The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation.
    Baes M, Gressens P, Huyghe S, De NK, Qi C, Jia Y, Mannaerts GP, Evrard P, Van VP, Declercq PE, Reddy JK.
    J Neuropathol Exp Neurol; 2002 Apr 28; 61(4):368-74. PubMed ID: 11939592
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  • 13. The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1.
    Waterham HR, de Vries Y, Russel KA, Xie W, Veenhuis M, Cregg JM.
    Mol Cell Biol; 1996 May 28; 16(5):2527-36. PubMed ID: 8628321
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  • 14. Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes.
    Nakayama M, Sato H, Okuda T, Fujisawa N, Kono N, Arai H, Suzuki E, Umeda M, Ishikawa HO, Matsuno K.
    PLoS One; 2011 May 28; 6(8):e22984. PubMed ID: 21826223
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  • 15. 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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  • 16. [Human peroxisome-deficient disorders and pathogenic gene].
    Fujiki Y.
    Rinsho Shinkeigaku; 1994 Dec 28; 34(12):1219-21. PubMed ID: 7539728
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  • 17. [Molecular biology of peroxisome biogenesis].
    Fujiki Y.
    Nihon Rinsho; 1993 Sep 28; 51(9):2336-42. PubMed ID: 8411711
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  • 18. Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.
    Infante JP, Huszagh VA.
    Mol Genet Metab; 2001 Jan 28; 72(1):1-7. PubMed ID: 11161822
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  • 19. [Biogenesis of peroxisome--targeting signal and peroxisome assembly factor].
    Fujiki Y.
    No To Hattatsu; 1992 Mar 28; 24(2):181-5. PubMed ID: 1567655
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