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294 related items for PubMed ID: 16775375

  • 21. Attenuation of MCP-1/CCL2 expression ameliorates neuropathy in a mouse model for Charcot-Marie-Tooth 1X.
    Groh J, Heinl K, Kohl B, Wessig C, Greeske J, Fischer S, Martini R.
    Hum Mol Genet; 2010 Sep 15; 19(18):3530-43. PubMed ID: 20591826
    [Abstract] [Full Text] [Related]

  • 22. Tetraspan myelin protein PMP22 and demyelinating peripheral neuropathies: new facts and hypotheses.
    Müller HW.
    Glia; 2000 Jan 15; 29(2):182-5. PubMed ID: 10625337
    [Abstract] [Full Text] [Related]

  • 23. Structure and stability of internodal myelin in mouse models of hereditary neuropathy.
    Avila RL, Inouye H, Baek RC, Yin X, Trapp BD, Feltri ML, Wrabetz L, Kirschner DA.
    J Neuropathol Exp Neurol; 2005 Nov 15; 64(11):976-90. PubMed ID: 16254492
    [Abstract] [Full Text] [Related]

  • 24. Origin of pathogenic macrophages and endoneurial fibroblast-like cells in an animal model of inherited neuropathy.
    Mäurer M, Müller M, Kobsar I, Leonhard C, Martini R, Kiefer R.
    Mol Cell Neurosci; 2003 Jul 15; 23(3):351-9. PubMed ID: 12837620
    [Abstract] [Full Text] [Related]

  • 25. Epitope-tagged P(0) glycoprotein causes Charcot-Marie-Tooth-like neuropathy in transgenic mice.
    Previtali SC, Quattrini A, Fasolini M, Panzeri MC, Villa A, Filbin MT, Li W, Chiu SY, Messing A, Wrabetz L, Feltri ML.
    J Cell Biol; 2000 Nov 27; 151(5):1035-46. PubMed ID: 11086005
    [Abstract] [Full Text] [Related]

  • 26. Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32.
    Kobsar I, Mäurer M, Ott T, Martini R.
    Neurosci Lett; 2002 Mar 01; 320(1-2):17-20. PubMed ID: 11849753
    [Abstract] [Full Text] [Related]

  • 27. The co-inhibitory molecule PD-1 modulates disease severity in a model for an inherited, demyelinating neuropathy.
    Kroner A, Schwab N, Ip CW, Sommer C, Wessig C, Wiendl H, Martini R.
    Neurobiol Dis; 2009 Jan 01; 33(1):96-103. PubMed ID: 18996482
    [Abstract] [Full Text] [Related]

  • 28. Endogenous antibodies contribute to macrophage-mediated demyelination in a mouse model for CMT1B.
    Klein D, Groh J, Weishaupt A, Martini R.
    J Neuroinflammation; 2015 Mar 12; 12():49. PubMed ID: 25879857
    [Abstract] [Full Text] [Related]

  • 29. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ.
    Acta Neurol Scand Suppl; 2012 Mar 12; (193):iv-22. PubMed ID: 23106488
    [Abstract] [Full Text] [Related]

  • 30. Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
    Fischer S, Kleinschnitz C, Müller M, Kobsar I, Ip CW, Rollins B, Martini R.
    Mol Cell Neurosci; 2008 Feb 12; 37(2):359-66. PubMed ID: 18326085
    [Abstract] [Full Text] [Related]

  • 31. Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice.
    Groh J, Basu R, Stanley ER, Martini R.
    J Neurosci; 2016 Feb 10; 36(6):1890-901. PubMed ID: 26865613
    [Abstract] [Full Text] [Related]

  • 32. Connexin32-null mice develop demyelinating peripheral neuropathy.
    Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ.
    Glia; 1998 Sep 10; 24(1):8-20. PubMed ID: 9700485
    [Abstract] [Full Text] [Related]

  • 33. Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.
    Rünker AE, Kobsar I, Fink T, Loers G, Tilling T, Putthoff P, Wessig C, Martini R, Schachner M.
    J Cell Biol; 2004 May 24; 165(4):565-73. PubMed ID: 15148307
    [Abstract] [Full Text] [Related]

  • 34. Electrophysiologic features of inherited demyelinating neuropathies: a reappraisal.
    Lewis RA, Sumner AJ.
    Ann N Y Acad Sci; 1999 Sep 14; 883():321-35. PubMed ID: 10586257
    [Abstract] [Full Text] [Related]

  • 35. Molecular genetics of inherited peripheral neuropathies: who are the actors?
    Meuleman J, Timmerman V, Nelis E, De Jonghe P.
    Acta Neurol Belg; 2000 Sep 14; 100(3):171-80. PubMed ID: 11098291
    [Abstract] [Full Text] [Related]

  • 36. Common themes in peripheral neuropathy disease genes.
    Snipes GJ, Orfali W.
    Cell Biol Int; 1998 Nov 14; 22(11-12):815-35. PubMed ID: 10873294
    [Abstract] [Full Text] [Related]

  • 37. Immune-mediated components of hereditary demyelinating neuropathies: lessons from animal models and patients.
    Martini R, Toyka KV.
    Lancet Neurol; 2004 Aug 14; 3(8):457-65. PubMed ID: 15261606
    [Abstract] [Full Text] [Related]

  • 38. Serum CXCL13 reflects local B-cell mediated inflammatory demyelinating peripheral neuropathy.
    Kim YH, Jang SY, Shin YK, Jo YR, Yoon BA, Nam SH, Choi BO, Shin HY, Kim SW, Kim SH, Kim JK, Park HT.
    Sci Rep; 2019 Nov 11; 9(1):16535. PubMed ID: 31712675
    [Abstract] [Full Text] [Related]

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