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

138 related items for PubMed ID: 18326085

  • 1. 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; 37(2):359-66. PubMed ID: 18326085
    [Abstract] [Full Text] [Related]

  • 2. Macrophage colony stimulating factor is a crucial factor for the intrinsic macrophage response in mice heterozygously deficient for the myelin protein P0.
    Müller M, Berghoff M, Kobsar I, Kiefer R, Martini R.
    Exp Neurol; 2007 Jan; 203(1):55-62. PubMed ID: 16962581
    [Abstract] [Full Text] [Related]

  • 3. Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.
    Fischer S, Weishaupt A, Troppmair J, Martini R.
    Glia; 2008 Jun; 56(8):836-43. PubMed ID: 18383340
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease.
    Martini R, Fischer S, López-Vales R, David S.
    Glia; 2008 Nov 01; 56(14):1566-1577. PubMed ID: 18803324
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Neuregulin 1-erbB signaling is necessary for normal myelination and sensory function.
    Chen S, Velardez MO, Warot X, Yu ZX, Miller SJ, Cros D, Corfas G.
    J Neurosci; 2006 Mar 22; 26(12):3079-86. PubMed ID: 16554459
    [Abstract] [Full Text] [Related]

  • 9. Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 gene.
    Berghoff M, Samsam M, Müller M, Kobsar I, Toyka KV, Kiefer R, Mäurer M, Martini R.
    Mol Cell Neurosci; 2005 Jan 22; 28(1):118-27. PubMed ID: 15607947
    [Abstract] [Full Text] [Related]

  • 10. Role of immune cells in animal models for inherited neuropathies: facts and visions.
    Mäurer M, Kobsar I, Berghoff M, Schmid CD, Carenini S, Martini R.
    J Anat; 2002 Apr 22; 200(4):405-14. PubMed ID: 12090406
    [Abstract] [Full Text] [Related]

  • 11. MCP-1/CCL2 modifies axon properties in a PMP22-overexpressing mouse model for Charcot-Marie-tooth 1A neuropathy.
    Kohl B, Fischer S, Groh J, Wessig C, Martini R.
    Am J Pathol; 2010 Mar 22; 176(3):1390-9. PubMed ID: 20093502
    [Abstract] [Full Text] [Related]

  • 12. Molecular mechanisms of inherited demyelinating neuropathies.
    Scherer SS, Wrabetz L.
    Glia; 2008 Nov 01; 56(14):1578-1589. PubMed ID: 18803325
    [Abstract] [Full Text] [Related]

  • 13. Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance.
    Schmid CD, Stienekemeier M, Oehen S, Bootz F, Zielasek J, Gold R, Toyka KV, Schachner M, Martini R.
    J Neurosci; 2000 Jan 15; 20(2):729-35. PubMed ID: 10632602
    [Abstract] [Full Text] [Related]

  • 14. Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.
    Kobsar I, Oetke C, Kroner A, Wessig C, Crocker P, Martini R.
    Mol Cell Neurosci; 2006 Apr 15; 31(4):685-91. PubMed ID: 16458537
    [Abstract] [Full Text] [Related]

  • 15. Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants.
    Mäurer M, Schmid CD, Bootz F, Zielasek J, Toyka KV, Oehen S, Martini R.
    Mol Cell Neurosci; 2001 Jun 15; 17(6):1094-101. PubMed ID: 11414797
    [Abstract] [Full Text] [Related]

  • 16. The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0.
    Carenini S, Mäurer M, Werner A, Blazyca H, Toyka KV, Schmid CD, Raivich G, Martini R.
    J Cell Biol; 2001 Jan 22; 152(2):301-8. PubMed ID: 11266447
    [Abstract] [Full Text] [Related]

  • 17. 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 22; 23(3):351-9. PubMed ID: 12837620
    [Abstract] [Full Text] [Related]

  • 18. Effects of the CC chemokine receptor 2 in mice deficient for the myelin protein zero (P0).
    Oberländer M, Berghoff M.
    Mol Cell Neurosci; 2010 Sep 22; 45(1):59-65. PubMed ID: 20553884
    [Abstract] [Full Text] [Related]

  • 19. Comparison of cytokine expression profile during Wallerian degeneration of myelinated and unmyelinated peripheral axons.
    Cheepudomwit T, Güzelsu E, Zhou C, Griffin JW, Höke A.
    Neurosci Lett; 2008 Jan 17; 430(3):230-5. PubMed ID: 18068300
    [Abstract] [Full Text] [Related]

  • 20. Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
    Martini R, Zielasek J, Toyka KV, Giese KP, Schachner M.
    Nat Genet; 1995 Nov 17; 11(3):281-6. PubMed ID: 7581451
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.