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Journal Abstract Search

265 related items for PubMed ID: 21487305

  • 1. Myelin and axon pathology in a long-term study of PMP22-overexpressing mice.
    Verhamme C, King RH, ten Asbroek AL, Muddle JR, Nourallah M, Wolterman R, Baas F, van Schaik IN.
    J Neuropathol Exp Neurol; 2011 May; 70(5):386-98. PubMed ID: 21487305
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  • 2. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.
    Adlkofer K, Martini R, Aguzzi A, Zielasek J, Toyka KV, Suter U.
    Nat Genet; 1995 Nov; 11(3):274-80. PubMed ID: 7581450
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  • 4. Regulation of myelin-specific gene expression. Relevance to CMT1.
    Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M.
    Ann N Y Acad Sci; 1999 Sep 14; 883():91-108. PubMed ID: 10586235
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  • 5. Evidence for macrophage-mediated myelin disruption in an animal model for Charcot-Marie-Tooth neuropathy type 1A.
    Kobsar I, Hasenpusch-Theil K, Wessig C, Müller HW, Martini R.
    J Neurosci Res; 2005 Sep 15; 81(6):857-64. PubMed ID: 16041800
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  • 6. Nerve conduction abnormalities and neuromyotonia in genetically engineered mouse models of human hereditary neuropathies.
    Zielasek J, Toyka KV.
    Ann N Y Acad Sci; 1999 Sep 14; 883():310-20. PubMed ID: 10586256
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  • 7. Uncoupling of neuroinflammation from axonal degeneration in mice lacking the myelin protein tetraspanin-2.
    de Monasterio-Schrader P, Patzig J, Möbius W, Barrette B, Wagner TL, Kusch K, Edgar JM, Brophy PJ, Werner HB.
    Glia; 2013 Nov 14; 61(11):1832-47. PubMed ID: 24038504
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  • 8. Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy.
    Meyer zu Horste G, Prukop T, Liebetanz D, Mobius W, Nave KA, Sereda MW.
    Ann Neurol; 2007 Jan 14; 61(1):61-72. PubMed ID: 17262851
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  • 10. PMP22 overexpression causes dysmyelination in mice.
    Robaglia-Schlupp A, Pizant J, Norreel JC, Passage E, Sabéran-Djoneidi D, Ansaldi JL, Vinay L, Figarella-Branger D, Lévy N, Clarac F, Cau P, Pellissier JF, Fontés M.
    Brain; 2002 Oct 14; 125(Pt 10):2213-21. PubMed ID: 12244079
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  • 11. Identification of the regulatory region of the peripheral myelin protein 22 (PMP22) gene that directs temporal and spatial expression in development and regeneration of peripheral nerves.
    Maier M, Berger P, Nave KA, Suter U.
    Mol Cell Neurosci; 2002 May 14; 20(1):93-109. PubMed ID: 12056842
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  • 13. Dysmyelination and reduced myelin basic protein gene expression by oligodendrocytes of SHP-1-deficient mice.
    Massa PT, Wu C, Fecenko-Tacka K.
    J Neurosci Res; 2004 Jul 01; 77(1):15-25. PubMed ID: 15197735
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  • 17. Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A.
    Perea J, Robertson A, Tolmachova T, Muddle J, King RH, Ponsford S, Thomas PK, Huxley C.
    Hum Mol Genet; 2001 May 01; 10(10):1007-18. PubMed ID: 11331611
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  • 20. Small axons relative to number of myelin lamellae in Charcot-Marie-Tooth disease 1A with peripheral myelin protein 22 gene duplication.
    Ohnishi A, Yamamoto T, Ikeda M.
    J UOEH; 2000 Jun 01; 22(2):107-17. PubMed ID: 10862406
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