Xu W, Yan J, Shao A, Lenahan C, Gao L, Wu H
Fundam Res. 2024; 4(6):1389-1397.
PMID: 39734532
PMC: 11670711.
DOI: 10.1016/j.fmre.2023.04.016.
Gonzalez-Rodriguez M, Marin-Valencia I
Cerebellum. 2023; 23(4):1626-1641.
PMID: 38123901
DOI: 10.1007/s12311-023-01641-2.
Deb R, Joshi N, Nagotu S
Neurotox Res. 2021; 39(3):986-1006.
PMID: 33400183
DOI: 10.1007/s12640-020-00323-9.
Abe Y, Nishimura Y, Nakamura K, Tamura S, Honsho M, Udo H
Front Cell Dev Biol. 2020; 8:567017.
PMID: 33163488
PMC: 7591468.
DOI: 10.3389/fcell.2020.567017.
Abe Y, Honsho M, Kawaguchi R, Matsuzaki T, Ichiki Y, Fujitani M
J Biol Chem. 2020; 295(16):5321-5334.
PMID: 32165495
PMC: 7170515.
DOI: 10.1074/jbc.RA119.011989.
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases.
Foschi M, Vacchiano V, Avoni P, Incensi A, Battaglia S, Donadio V
Front Neurol. 2019; 10:70.
PMID: 30787906
PMC: 6372518.
DOI: 10.3389/fneur.2019.00070.
Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum.
Abe Y, Honsho M, Itoh R, Kawaguchi R, Fujitani M, Fujiwara K
Life Sci Alliance. 2018; 1(6):e201800062.
PMID: 30519675
PMC: 6277683.
DOI: 10.26508/lsa.201800062.
Peroxisomes in brain development and function.
Berger J, Dorninger F, Forss-Petter S, Kunze M
Biochim Biophys Acta. 2015; 1863(5):934-55.
PMID: 26686055
PMC: 4880039.
DOI: 10.1016/j.bbamcr.2015.12.005.
Peroxisomal Disorders: A Review on Cerebellar Pathologies.
De Munter S, Verheijden S, Regal L, Baes M
Brain Pathol. 2015; 25(6):663-78.
PMID: 26201894
PMC: 8029412.
DOI: 10.1111/bpa.12290.
PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress.
Muller C, Nguyen T, Ahlemeyer B, Meshram M, Santrampurwala N, Cao S
Dis Model Mech. 2010; 4(1):104-19.
PMID: 20959636
PMC: 3014351.
DOI: 10.1242/dmm.004622.
Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration.
Hulshagen L, Krysko O, Bottelbergs A, Huyghe S, Klein R, Van Veldhoven P
J Neurosci. 2008; 28(15):4015-27.
PMID: 18400901
PMC: 6670456.
DOI: 10.1523/JNEUROSCI.4968-07.2008.
The peroxisome: still a mysterious organelle.
Schrader M, Fahimi H
Histochem Cell Biol. 2008; 129(4):421-40.
PMID: 18274771
PMC: 2668598.
DOI: 10.1007/s00418-008-0396-9.
Contribution of fetal MR imaging in the prenatal diagnosis of Zellweger syndrome.
Mochel F, Grebille A, Benachi A, Martinovic J, Razavi F, Rabier D
AJNR Am J Neuroradiol. 2006; 27(2):333-6.
PMID: 16484405
PMC: 8148762.
Peroxisomal biogenesis disorder: comparison of conventional MR imaging with diffusion-weighted and diffusion-tensor imaging findings.
ter Rahe B, Majoie C, Akkerman E, den Heeten G, Poll-The B, Barth P
AJNR Am J Neuroradiol. 2004; 25(6):1022-7.
PMID: 15205141
PMC: 7975665.
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
J Neurosci. 2003; 23(30):9732-41.
PMID: 14586000
PMC: 6740889.
The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction.
Faust P, Su H, Moser A, Moser H
J Mol Neurosci. 2001; 16(2-3):289-97; discussion 317-21.
PMID: 11478384
DOI: 10.1385/JMN:16:2-3:289.
Identifying homologous anatomical landmarks on reconstructed magnetic resonance images of the human cerebral cortical surface.
Maudgil D, Free S, Sisodiya S, Lemieux L, Woermann F, Fish D
J Anat. 1999; 193 ( Pt 4):559-71.
PMID: 10029189
PMC: 1467881.
DOI: 10.1046/j.1469-7580.1998.19340559.x.
Peroxisomal disorders: genotype, phenotype, major neuropathologic lesions, and pathogenesis.
Powers J, Moser H
Brain Pathol. 1998; 8(1):101-20.
PMID: 9458170
PMC: 8098283.
DOI: 10.1111/j.1750-3639.1998.tb00139.x.
Dentato-olivary dysplasia in sibs: an autosomal recessive disorder?.
Martland T, Harding B, MORTON R, Young I
J Med Genet. 1998; 34(12):1021-3.
PMID: 9429148
PMC: 1051157.
DOI: 10.1136/jmg.34.12.1021.
Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.
Faust P, Hatten M
J Cell Biol. 1998; 139(5):1293-305.
PMID: 9382874
PMC: 2140200.
DOI: 10.1083/jcb.139.5.1293.