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239 related items for PubMed ID: 17075904

  • 1. Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver.
    Krysko O, Hulshagen L, Janssen A, Schütz G, Klein R, De Bruycker M, Espeel M, Gressens P, Baes M.
    J Neurosci Res; 2007 Jan; 85(1):58-72. PubMed ID: 17075904
    [Abstract] [Full Text] [Related]

  • 2. Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities.
    Dirkx R, Vanhorebeek I, Martens K, Schad A, Grabenbauer M, Fahimi D, Declercq P, Van Veldhoven PP, Baes M.
    Hepatology; 2005 Apr; 41(4):868-78. PubMed ID: 15732085
    [Abstract] [Full Text] [Related]

  • 3. 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; 17(1):49-57. PubMed ID: 9288097
    [Abstract] [Full Text] [Related]

  • 4. Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency.
    Faust PL.
    J Comp Neurol; 2003 Jun 30; 461(3):394-413. PubMed ID: 12746876
    [Abstract] [Full Text] [Related]

  • 5. A review of morphological techniques for detection of peroxisomal (and mitochondrial) proteins and their corresponding mRNAs during ontogenesis in mice: application to the PEX5-knockout mouse with Zellweger syndrome.
    Baumgart E, Fahimi HD, Steininger H, Grabenbauer M.
    Microsc Res Tech; 2003 Jun 01; 61(2):121-38. PubMed ID: 12740819
    [Abstract] [Full Text] [Related]

  • 6. Axonal integrity in the absence of functional peroxisomes from projection neurons and astrocytes.
    Bottelbergs A, Verheijden S, Hulshagen L, Gutmann DH, Goebbels S, Nave KA, Kassmann C, Baes M.
    Glia; 2010 Oct 01; 58(13):1532-43. PubMed ID: 20578053
    [Abstract] [Full Text] [Related]

  • 7. Close homologue of adhesion molecule L1 promotes survival of Purkinje and granule cells and granule cell migration during murine cerebellar development.
    Jakovcevski I, Siering J, Hargus G, Karl N, Hoelters L, Djogo N, Yin S, Zecevic N, Schachner M, Irintchev A.
    J Comp Neurol; 2009 Apr 10; 513(5):496-510. PubMed ID: 19226508
    [Abstract] [Full Text] [Related]

  • 8. Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.
    Nagase T, Shimozawa N, Takemoto Y, Suzuki Y, Komori M, Kondo N.
    Biochim Biophys Acta; 2004 Mar 17; 1671(1-3):26-33. PubMed ID: 15026142
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse).
    Baumgart E, Vanhorebeek I, Grabenbauer M, Borgers M, Declercq PE, Fahimi HD, Baes M.
    Am J Pathol; 2001 Oct 17; 159(4):1477-94. PubMed ID: 11583975
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain.
    Ahlemeyer B, Neubert I, Kovacs WJ, Baumgart-Vogt E.
    J Comp Neurol; 2007 Nov 01; 505(1):1-17. PubMed ID: 17729295
    [Abstract] [Full Text] [Related]

  • 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 Nov 01; 16(2-3):289-97; discussion 317-21. PubMed ID: 11478384
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 61(4):368-74. PubMed ID: 11939592
    [Abstract] [Full Text] [Related]

  • 14. Role of Clast1 in development of cerebellar granule cells.
    Maeda Y, Fujimura L, O-Wang J, Hatano M, Sakamoto A, Arima M, Ebara M, Ino H, Yamashita T, Saisho H, Tokuhisa T.
    Brain Res; 2006 Aug 09; 1104(1):18-26. PubMed ID: 16814752
    [Abstract] [Full Text] [Related]

  • 15. 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 09; 72(1):1-7. PubMed ID: 11161822
    [Abstract] [Full Text] [Related]

  • 16. Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.
    Brites P, Motley AM, Gressens P, Mooyer PA, Ploegaert I, Everts V, Evrard P, Carmeliet P, Dewerchin M, Schoonjans L, Duran M, Waterham HR, Wanders RJ, Baes M.
    Hum Mol Genet; 2003 Sep 15; 12(18):2255-67. PubMed ID: 12915479
    [Abstract] [Full Text] [Related]

  • 17. Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues.
    Janssen A, Gressens P, Grabenbauer M, Baumgart E, Schad A, Vanhorebeek I, Brouwers A, Declercq PE, Fahimi D, Evrard P, Schoonjans L, Collen D, Carmeliet P, Mannaerts G, Van Veldhoven P, Baes M.
    J Neurosci; 2003 Oct 29; 23(30):9732-41. PubMed ID: 14586000
    [Abstract] [Full Text] [Related]

  • 18. Abnormal neocortical development in mice lacking cGMP-dependent protein kinase I.
    Demyanenko GP, Halberstadt AI, Pryzwansky KB, Werner C, Hofmann F, Maness PF.
    Brain Res Dev Brain Res; 2005 Nov 07; 160(1):1-8. PubMed ID: 16154207
    [Abstract] [Full Text] [Related]

  • 19. Cerebellar defects in Pdss2 conditional knockout mice during embryonic development and in adulthood.
    Lu S, Lu LY, Liu MF, Yuan QJ, Sham MH, Guan XY, Huang JD.
    Neurobiol Dis; 2012 Jan 07; 45(1):219-33. PubMed ID: 21871565
    [Abstract] [Full Text] [Related]

  • 20. Mass spectrometric analysis of ceramide perturbations in brain and fibroblasts of mice and human patients with peroxisomal disorders.
    Pettus BJ, Baes M, Busman M, Hannun YA, Van Veldhoven PP.
    Rapid Commun Mass Spectrom; 2004 Jan 07; 18(14):1569-74. PubMed ID: 15282781
    [Abstract] [Full Text] [Related]

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