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Journal Abstract Search

258 related items for PubMed ID: 12897163

  • 1. 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; 23(16):5947-57. PubMed ID: 12897163
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  • 2. Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.
    Krause C, Rosewich H, Woehler A, Gärtner J.
    Hum Mol Genet; 2013 Oct 01; 22(19):3844-57. PubMed ID: 23716570
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  • 3. 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
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  • 4. A mouse model for Zellweger syndrome.
    Baes M, Gressens P, Baumgart E, Carmeliet P, Casteels M, Fransen M, Evrard P, Fahimi D, Declercq PE, Collen D, van Veldhoven PP, Mannaerts GP.
    Nat Genet; 1997 Sep 15; 17(1):49-57. PubMed ID: 9288097
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  • 5. Peroxisomal protein PEX13 functions in selective autophagy.
    Lee MY, Sumpter R, Zou Z, Sirasanagandla S, Wei Y, Mishra P, Rosewich H, Crane DI, Levine B.
    EMBO Rep; 2017 Jan 15; 18(1):48-60. PubMed ID: 27827795
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  • 6. 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 15; 61(4):368-74. PubMed ID: 11939592
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  • 11. 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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  • 12. 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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  • 13. 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 01; 67(4):967-75. PubMed ID: 10958759
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  • 14. Mitochondrial changes and oxidative stress in a mouse model of Zellweger syndrome neuropathogenesis.
    Rahim RS, Chen M, Nourse CC, Meedeniya AC, Crane DI.
    Neuroscience; 2016 Oct 15; 334():201-213. PubMed ID: 27514574
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  • 15. Identification of a novel PEX14 mutation in Zellweger syndrome.
    Huybrechts SJ, Van Veldhoven PP, Hoffman I, Zeevaert R, de Vos R, Demaerel P, Brams M, Jaeken J, Fransen M, Cassiman D.
    J Med Genet; 2008 Jun 15; 45(6):376-83. PubMed ID: 18285423
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  • 16. Central serotonergic neuron deficiency in a mouse model of Zellweger syndrome.
    Rahim RS, Meedeniya AC, Crane DI.
    Neuroscience; 2014 Aug 22; 274():229-41. PubMed ID: 24881576
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  • 20. Impaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiency.
    Rahim RS, St John JA, Crane DI, Meedeniya ACB.
    Mol Cell Neurosci; 2018 Apr 22; 88():16-32. PubMed ID: 29187321
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