Martini R - Search Results

1

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. Groh J, et al. Among authors: martini r. Hum Mol Genet. 2010 Sep 15;19(18):3530-43. doi: 10.1093/hmg/ddq269. Epub 2010 Jun 30. Hum Mol Genet. 2010. PMID: 20591826

2

Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium.

Müller HW, Suter U, Van Broeckhoven C, Hanemann CO, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreëls-Festen A, Gillen C, Haites N, Levi G, Mariman E, Martini R, Nave K, Rautenstrauss B, Schachner M, Schenone A, Schneider C, Schröder M, Willecke K. Müller HW, et al. Among authors: martini r. Neurobiol Dis. 1997;4(3-4):215-20. doi: 10.1006/nbdi.1997.0148. Neurobiol Dis. 1997. PMID: 9361297 Review.

3

Inherited demyelinating neuropathies: from gene to disease.

Martini R, Zielasek J, Toyka KV. Martini R, et al. Curr Opin Neurol. 1998 Oct;11(5):545-56. doi: 10.1097/00019052-199810000-00018. Curr Opin Neurol. 1998. PMID: 9848005 Review.

4

P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.

Martini R. Martini R. Ann N Y Acad Sci. 1999 Sep 14;883:273-80. Ann N Y Acad Sci. 1999. PMID: 10586252 Review.

5

Miller Fisher syndrome: immunofluorescence and immunoelectron microscopic localization of IgG at the mouse neuromuscular junction.

Wessig C, Buchwald B, Toyka KV, Martini R. Wessig C, et al. Among authors: martini r. Acta Neuropathol. 2001 Mar;101(3):239-44. doi: 10.1007/s004010000285. Acta Neuropathol. 2001. PMID: 11307623

6

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. Mäurer M, et al. Among authors: martini r. J Anat. 2002 Apr;200(4):405-14. doi: 10.1046/j.1469-7580.2002.00045.x. J Anat. 2002. PMID: 12090406 Free PMC article. Review.

7

Preserved myelin integrity and reduced axonopathy in connexin32-deficient mice lacking the recombination activating gene-1.

Kobsar I, Berghoff M, Samsam M, Wessig C, Mäurer M, Toyka KV, Martini R. Kobsar I, et al. Among authors: martini r. Brain. 2003 Apr;126(Pt 4):804-13. doi: 10.1093/brain/awg072. Brain. 2003. PMID: 12615640

8

The Wlds mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy.

Samsam M, Mi W, Wessig C, Zielasek J, Toyka KV, Coleman MP, Martini R. Samsam M, et al. Among authors: martini r. J Neurosci. 2003 Apr 1;23(7):2833-9. doi: 10.1523/JNEUROSCI.23-07-02833.2003. J Neurosci. 2003. PMID: 12684470 Free PMC article.

9

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. Mäurer M, et al. Among authors: martini r. Mol Cell Neurosci. 2003 Jul;23(3):351-9. doi: 10.1016/s1044-7431(03)00055-1. Mol Cell Neurosci. 2003. PMID: 12837620

10

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. Rünker AE, et al. Among authors: martini r. J Cell Biol. 2004 May 24;165(4):565-73. doi: 10.1083/jcb.200402087. Epub 2004 May 17. J Cell Biol. 2004. PMID: 15148307 Free PMC article.

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