These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

283 related items for PubMed ID: 15555916

  • 1. Peripheral myelin protein 22 kDa and protein zero: domain specific trans-interactions.
    Hasse B, Bosse F, Hanenberg H, Müller HW.
    Mol Cell Neurosci; 2004 Dec; 27(4):370-8. PubMed ID: 15555916
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases.
    Shames I, Fraser A, Colby J, Orfali W, Snipes GJ.
    J Neuropathol Exp Neurol; 2003 Jul; 62(7):751-64. PubMed ID: 12901701
    [Abstract] [Full Text] [Related]

  • 3. Mutations in demyelinating peripheral neuropathies support molecular model of myelin P0-glycoprotein extracellular domain.
    Kirschner DA, Saavedra RA.
    J Neurosci Res; 1994 Sep 01; 39(1):63-9. PubMed ID: 7528817
    [Abstract] [Full Text] [Related]

  • 4. Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.
    Huehne K, Benes V, Thiel C, Kraus C, Kress W, Hoeltzenbein M, Ploner CJ, Kotzian J, Reis A, Rott HD, Rautenstrauss BW.
    Hum Mutat; 2003 Jan 01; 21(1):100. PubMed ID: 12497641
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Molecular genetics of inherited peripheral neuropathies: who are the actors?
    Meuleman J, Timmerman V, Nelis E, De Jonghe P.
    Acta Neurol Belg; 2000 Sep 01; 100(3):171-80. PubMed ID: 11098291
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.
    Himoro M, Yoshikawa H, Matsui T, Mitsui Y, Takahashi M, Kaido M, Nishimura T, Sawaishi Y, Takada G, Hayasaka K.
    Biochem Mol Biol Int; 1993 Sep 01; 31(1):169-73. PubMed ID: 7505151
    [Abstract] [Full Text] [Related]

  • 10. Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
    Carenini S, Neuberg D, Schachner M, Suter U, Martini R.
    Glia; 1999 Dec 01; 28(3):256-64. PubMed ID: 10559784
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.
    Mostacciuolo ML, Righetti E, Zortea M, Bosello V, Schiavon F, Vallo L, Merlini L, Siciliano G, Fabrizi GM, Rizzuto N, Milani M, Baratta S, Taroni F.
    Hum Mutat; 2001 Dec 01; 18(1):32-41. PubMed ID: 11438991
    [Abstract] [Full Text] [Related]

  • 14. Recombinant peripheral myelin protein P0 confers both adhesion and neurite outgrowth-promoting properties.
    Schneider-Schaulies J, von Brunn A, Schachner M.
    J Neurosci Res; 1990 Nov 01; 27(3):286-97. PubMed ID: 1711125
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 20(1):93-109. PubMed ID: 12056842
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32), peripheral myelin protein 22 (PMP22), and peripheral myelin protein zero (MPZ).
    Ekici AB, Schweitzer D, Park O, Lorek D, Rautenstrauss B, Krüger G, Friedl W, Uhlhaas S, Bathke K, Heuss D, Kayser C, Grehl H.
    Neurogenetics; 2000 Sep 14; 3(1):49-50. PubMed ID: 11085599
    [No Abstract] [Full Text] [Related]

  • 18. A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
    Kochanski A, Drac H, Kabzińska D, Hausmanowa-Petrusewicz I.
    Neuromuscul Disord; 2004 Mar 14; 14(3):229-32. PubMed ID: 15036333
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.