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Journal Abstract Search

584 related items for PubMed ID: 9672419

  • 1. Many facets of the peripheral myelin protein PMP22 in myelination and disease.
    Naef R, Suter U.
    Microsc Res Tech; 1998 Jun 01; 41(5):359-71. PubMed ID: 9672419
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 14; 11(3):274-80. PubMed ID: 7581450
    [Abstract] [Full Text] [Related]

  • 4. New vistas on the pathomechanism of Charcot-Marie-Tooth and related peripheral neuropathies.
    Müller HW.
    Ann N Y Acad Sci; 1999 Sep 14; 883():152-9. PubMed ID: 10586241
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.
    Nelis E, Haites N, Van Broeckhoven C.
    Hum Mutat; 1999 May 14; 13(1):11-28. PubMed ID: 9888385
    [Abstract] [Full Text] [Related]

  • 7. Peripheral myelin protein 22: facts and hypotheses.
    Suter U, Snipes GJ.
    J Neurosci Res; 1995 Feb 01; 40(2):145-51. PubMed ID: 7745607
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  • 11. Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development.
    Baechner D, Liehr T, Hameister H, Altenberger H, Grehl H, Suter U, Rautenstrauss B.
    J Neurosci Res; 1995 Dec 15; 42(6):733-41. PubMed ID: 8847735
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  • 12. [Molecular pathology of Charcot-Marie-Tooth disease type 1A: abnormal expression of PMP-22].
    Yoshikawa H, Nishimura T, Yanagihara T.
    Rinsho Shinkeigaku; 1995 Dec 15; 35(12):1441-3. PubMed ID: 8752424
    [Abstract] [Full Text] [Related]

  • 13. Transgenic mouse models of CMT1A and HNPP.
    Suter U, Nave KA.
    Ann N Y Acad Sci; 1999 Sep 14; 883():247-53. PubMed ID: 10586249
    [Abstract] [Full Text] [Related]

  • 14. Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
    Resko P, Radvansky J, Odnogova Z, Baldovic M, Minarik G, Polakova H, Palffy R, Kadasi L.
    Gen Physiol Biophys; 2011 Dec 14; 30(4):379-88. PubMed ID: 22131320
    [Abstract] [Full Text] [Related]

  • 15. Charcot-Marie-Tooth disease and related inherited neuropathies.
    Murakami T, Garcia CA, Reiter LT, Lupski JR.
    Medicine (Baltimore); 1996 Sep 14; 75(5):233-50. PubMed ID: 8862346
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of hereditary neuropathies.
    Chance PF.
    Phys Med Rehabil Clin N Am; 2001 May 14; 12(2):277-91. PubMed ID: 11345007
    [Abstract] [Full Text] [Related]

  • 17. The peripheral myelin protein 22 and epithelial membrane protein family.
    Jetten AM, Suter U.
    Prog Nucleic Acid Res Mol Biol; 2000 May 14; 64():97-129. PubMed ID: 10697408
    [Abstract] [Full Text] [Related]

  • 18. Molecular alterations resulting from frameshift mutations in peripheral myelin protein 22: implications for neuropathy severity.
    Johnson JS, Roux KJ, Fletcher BS, Fortun J, Notterpek L.
    J Neurosci Res; 2005 Dec 15; 82(6):743-52. PubMed ID: 16273544
    [Abstract] [Full Text] [Related]

  • 19. Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1A.
    Haney C, Snipes GJ, Shooter EM, Suter U, Garcia C, Griffin JW, Trapp BD.
    J Neuropathol Exp Neurol; 1996 Mar 15; 55(3):290-9. PubMed ID: 8786387
    [Abstract] [Full Text] [Related]

  • 20. Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease.
    Nobbio L, Vigo T, Abbruzzese M, Levi G, Brancolini C, Mantero S, Grandis M, Benedetti L, Mancardi G, Schenone A.
    Neurobiol Dis; 2004 Jun 15; 16(1):263-73. PubMed ID: 15207283
    [Abstract] [Full Text] [Related]

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