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Rudolf Martini

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Janos Groh; Chi Wang Ip; Thomas G Kühl; Thomas Langmann; Jonathan D Cooper; Steven Duckett; Myriam Mirza; Hemanth R Nelvagal; Sarmi Sri; Rudolf Martini
Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosis.
Chi Wang Ip; Dennis Klein; Antje Kroner; Ricarda Diem; Julia M Edgar; Janos Groh; Marianne Huber; Klaus-Armin Nave; Irene Spahn; Sarah K Williams; Rudolf Martini
Neuroinflammation by cytotoxic T-lymphocytes impairs retrograde axonal transport in an oligodendrocyte mutant mouse.
Janos Groh; Heike Heuer; E Richard Stanley; Joachim Weis; Hanna Zieger; Rudolf Martini
Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot-Marie-Tooth disease type 1X.

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2013: Janos Groh; Chi Wang Ip; Thomas G Kühl; Thomas Langmann; Jonathan D Cooper; Steven Duckett; Myriam Mirza; Hemanth R Nelvagal; Sarmi Sri; Rudolf Martini
Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosis.
Brain : a journal of neurology 2013;136(Pt 4):1083-101.
2012: Chi Wang Ip; Dennis Klein; Antje Kroner; Ricarda Diem; Julia M Edgar; Janos Groh; Marianne Huber; Klaus-Armin Nave; Irene Spahn; Sarah K Williams; Rudolf Martini
Neuroinflammation by cytotoxic T-lymphocytes impairs retrograde axonal transport in an oligodendrocyte mutant mouse.
PloS one 2012;7(8):e42554.
2012: Janos Groh; Heike Heuer; E Richard Stanley; Joachim Weis; Hanna Zieger; Rudolf Martini
Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot-Marie-Tooth disease type 1X.
Brain : a journal of neurology 2012;135(Pt 1):88-104.
2010: Bianca Kohl; Janos Groh; Carsten Wessig; Heinz Wiendl; Antje Kroner; Rudolf Martini
Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A.
Neurobiology of disease 2010;38(1):78-84.
2010: Bianca Kohl; Stefan Fischer; Janos Groh; Carsten Wessig; Rudolf Martini
MCP-1/CCL2 modifies axon properties in a PMP22-overexpressing mouse model for Charcot-Marie-tooth 1A neuropathy.
The American journal of pathology 2010;176(3):1390-9.
2010: Antje Kroner; Chi Wang Ip; Johannes Thalhammer; Klaus-Armin Nave; Rudolf Martini
Ectopic T-cell specificity and absence of perforin and granzyme B alleviate neural damage in oligodendrocyte mutant mice.
The American journal of pathology 2010;176(2):549-55.
2009: Antje Kroner; Nicholas Schwab; Chi Wang Ip; Sonja Ortler; Kerstin Göbel; Klaus-Armin Nave; Mathias Mäurer; Rudolf Martini; Heinz Wiendl
Accelerated course of experimental autoimmune encephalomyelitis in PD-1-deficient central nervous system myelin mutants.
The American journal of pathology 2009;174(6):2290-9.
2009: Chi Wang Ip; Antje Kroner; Bianca Kohl; Carsten Wessig; Rudolf Martini
Tacrolimus (FK506) causes disease aggravation in models for inherited peripheral myelinopathies.
Neurobiology of disease 2009;33(2):207-12.
2009: Antje Kroner; Nicholas Schwab; Chi Wang Ip; Christoph Leder; Klaus-Armin Nave; Mathias Mäurer; Heinz Wiendl; Rudolf Martini
PD-1 regulates neural damage in oligodendroglia-induced inflammation.
PloS one 2009;4(2):e4405.
2008: Rudolf Martini; Stefan Fischer; Rubèn López-Vales; Samuel David
Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease.
Glia 2008;56(14):1566-77.
2008: Chi Wang Ip; Bianca Kohl; Christoph Kleinschnitz; Bernhard Reuss; Klaus-Armin Nave; Antje Kroner; Rudolf Martini
Origin of CD11b+ macrophage-like cells in the CNS of PLP-overexpressing mice: low influx of haematogenous macrophages and unchanged blood-brain-barrier in the optic nerve.
Molecular and cellular neurosciences 2008;38(4):489-94.
2008: Stefan Fischer; Andreas Weishaupt; Jakob Troppmair; Rudolf Martini
Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.
Glia 2008;56(8):836-43.
2008: Stefan Fischer; Christoph Kleinschnitz; Marcus Müller; Igor Kobsar; Chi Wang Ip; Barrett Rollins; Rudolf Martini
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
Molecular and cellular neurosciences 2008;37(2):359-66.
2007: Christoph Leder; N Schwab; Chi Wang Ip; Antje Kroner; Klaus-Armin Nave; Klaus Dornmair; Rudolf Martini; Heinz Wiendl
Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice.
Molecular and cellular neurosciences 2007;36(3):416-24.
2007: Birgit Ey; Igor Kobsar; Heinrich Blazyca; Antje Kroner; Rudolf Martini
Visualization of degenerating axons in a dysmyelinating mouse mutant with axonal loss.
Molecular and cellular neurosciences 2007;35(1):153-60.
2007: Chi Wang Ip; Antje Kroner; Paul R Crocker; Klaus-Armin Nave; Rudolf Martini
Sialoadhesin deficiency ameliorates myelin degeneration and axonopathic changes in the CNS of PLP overexpressing mice.
Neurobiology of disease 2007;25(1):105-11.
2007: Marcus Müller; Martin Berghoff; Igor Kobsar; Reinhard Kiefer; Rudolf Martini
Macrophage colony stimulating factor is a crucial factor for the intrinsic macrophage response in mice heterozygously deficient for the myelin protein P0.
Experimental neurology 2007;203(1):55-62.
2006: Chi Wang Ip; Antje Kroner; Martin Bendszus; Christoph Leder; Igor Kobsar; Stefan Fischer; Heinz Wiendl; Klaus-Armin Nave; Rudolf Martini
Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(31):8206-16.
2006: Nurcan Üçeyler; Igor Kobsar; Lydia Biko; Jochen C Ulzheimer; S Rock Levinson; Rudolf Martini; Claudia Sommer
Heterozygous P0 deficiency protects mice from vincristine-induced polyneuropathy.
Journal of neuroscience research 2006;84(1):37-46.
2006: Igor Kobsar; Cornelia Oetke; Antje Kroner; Carsten Wessig; Paul Crocker; Rudolf Martini
Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.
Molecular and cellular neurosciences 2006;31(4):685-91.
2006: Chi Wang Ip; Antje Kroner; Stefan Fischer; Martin Berghoff; Igor Kobsar; Mathias Mäurer; Rudolf Martini
Role of immune cells in animal models for inherited peripheral neuropathies.
Neuromolecular medicine 2006;8(1-2):175-90.
2005: Igor Kobsar; Kerstin Hasenpusch-Theil; Carsten Wessig; Hans Werner Müller; Rudolf Martini
Evidence for macrophage-mediated myelin disruption in an animal model for Charcot-Marie-Tooth neuropathy type 1A.
Journal of neuroscience research 2005;81(6):857-64.
2005: Bettina Holtmann; Stefan Wiese; Mohtashem Samsam; Katja Grohmann; Diane Pennica; Rudolf Martini; Michael Sendtner
Triple knock-out of CNTF, LIF, and CT-1 defines cooperative and distinct roles of these neurotrophic factors for motoneuron maintenance and function.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2005;25(7):1778-87.
2005: Martin Berghoff; Mohtashem Samsam; Marcus Müller; Igor Kobsar; Klaus V Toyka; Reinhard Kiefer; Mathias Mäurer; Rudolf Martini
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.
Molecular and cellular neurosciences 2005;28(1):118-27.
2004: Katja Grohmann; wilfried rossoll; Igor Kobsar; Bettina Holtmann; Sibylle Jablonka; Carsten Wessig; Gisela Stoltenburg-Didinger; Utz Fischer; Christoph Hübner; Rudolf Martini; Michael Sendtner
Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Human molecular genetics 2004;13(18):2031-42.
2004: Rudolf Martini; Klaus V Toyka
Immune-mediated components of hereditary demyelinating neuropathies: lessons from animal models and patients.
Lancet neurology 2004;3(8):457-65.
2004: Annette Rünker; Igor Kobsar; Torsten Fink; Gabriele Loers; Thomas Tilling; Peggy Putthoff; Carsten Wessig; Rudolf Martini; Melitta Schachner
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.
The Journal of cell biology 2004;165(4):565-73.
2004: Jochen C Ulzheimer; Elior Peles; S Rock Levinson; Rudolf Martini
Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants.
Molecular and cellular neurosciences 2004;25(1):83-94.
2003: Mathias Mäurer; Marcus Müller; Igor Kobsar; Christine Leonhard; Rudolf Martini; Reinhard Kiefer
Origin of pathogenic macrophages and endoneurial fibroblast-like cells in an animal model of inherited neuropathy.
Molecular and cellular neurosciences 2003;23(3):351-9.
2003: Mohtashem Samsam; Weiqian Mi; Carsten Wessig; Jürgen Zielasek; Klaus V Toyka; Michael P Coleman; Rudolf Martini
The Wlds mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2003;23(7):2833-9.
2003: Igor Kobsar; Martin Berghoff; Mohtashem Samsam; Carsten Wessig; Mathias Mäurer; Klaus V Toyka; Rudolf Martini
Preserved myelin integrity and reduced axonopathy in connexin32-deficient mice lacking the recombination activating gene-1.
Brain : a journal of neurology 2003;126(Pt 4):804-13.
2002: Ralf A Linker; Mathias Mäurer; Stefanie Gaupp; Rudolf Martini; Bettina Holtmann; Ralf Giess; Peter Rieckmann; Hans Lassmann; Klaus V Toyka; Michael Sendtner; Ralf Gold
CNTF is a major protective factor in demyelinating CNS disease: a neurotrophic cytokine as modulator in neuroinflammation.
Nature medicine 2002;8(6):620-4.
2002: Mathias Mäurer; Igor Kobsar; Martin Berghoff; Christoph D Schmid; Stefano Carenini; Rudolf Martini
Role of immune cells in animal models for inherited neuropathies: facts and visions.
Journal of anatomy 2002;200(4):405-14.
2002: Igor Kobsar; Mathias Mäurer; Thomas Ott; Rudolf Martini
Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32.
Neuroscience letters 2002;320(1-2):17-20.
2002: Mohtashem Samsam; R Frei; Martin Marziniak; Rudolf Martini; Claudia Sommer
Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves.
Journal of neuroscience research 2002;67(2):167-73.
2001: Mathias Mäurer; Christoph D Schmid; F Bootz; Jürgen Zielasek; Klaus V Toyka; S Oehen; Rudolf Martini
Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants.
Molecular and cellular neurosciences 2001;17(6):1094-101.
2001: Rudolf Martini
The effect of myelinating Schwann cells on axons.
Muscle & nerve 2001;24(4):456-66.
2001: Carsten Wessig; Brigitte Buchwald; Klaus V Toyka; Rudolf Martini
Miller Fisher syndrome: immunofluorescence and immunoelectron microscopic localization of IgG at the mouse neuromuscular junction.
Acta neuropathologica 2001;101(3):239-44.
2001: Stefano Carenini; Mathias Mäurer; A Werner; H Blazyca; Klaus V Toyka; Christoph D Schmid; G Raivich; Rudolf Martini
The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0.
The Journal of cell biology 2001;152(2):301-8.
2000: Rudolf Martini
Animal models for inherited peripheral neuropathies: chances to find treatment strategies?
Journal of neuroscience research 2000;61(3):244-50.
2000: Jürgen Zielasek; Rudolf Martini; U Suter; Klaus V Toyka
Neuromyotonia in mice with hereditary myelinopathies.
Muscle & nerve 2000;23(5):696-701.
2000: Christoph D Schmid; Martina Stienekemeier; S Oehen; F Bootz; Jürgen Zielasek; Ralf Gold; Klaus V Toyka; M Schachner; Rudolf Martini
Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2000;20(2):729-35.
1999: Stefano Carenini; D Neuberg; Melitta Schachner; Ueli Suter; Rudolf Martini
Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
Glia 1999;28(3):256-64.
1999: Rudolf Martini
P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.
Annals of the New York Academy of Sciences 1999;883():273-80.
1999: R Frei; James Dowling; Stefano Carenini; E Fuchs; Rudolf Martini
Myelin formation by Schwann cells in the absence of beta4 integrin.
Glia 1999;27(3):269-74.
1999: Stefano Carenini; Dirk Montag; Melitta Schachner; Rudolf Martini
Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice.
Glia 1999;27(3):203-12.
1999: R Frei; S Mötzing; Ilka Kinkelin; M Schachner; Martin Koltzenburg; Rudolf Martini
Loss of distal axons and sensory Merkel cells and features indicative of muscle denervation in hindlimbs of P0-deficient mice.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1999;19(14):6058-67.
1999: RL Lindberg; Rudolf Martini; M Baumgartner; Beat Erne; J Borg; Jürgen Zielasek; K Ricker; A Steck; K V Toyka; Urs A Meyer
Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyria.
The Journal of clinical investigation 1999;103(8):1127-34.
1999: V Guénard; Beat Schweitzer; E Flechsig; S Hemmi; Rudolf Martini; Ueli Suter; Melitta Schachner
Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice.
Glia 1999;25(2):165-78.
1998: Rudolf Martini; Jürgen Zielasek; Klaus V Toyka
Inherited demyelinating neuropathies: from gene to disease.
Current opinion in neurology 1998;11(5):545-56.
1998: DH Neuberg; Stefano Carenini; Melitta Schachner; Rudolf Martini; Ueli Suter
Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero.
Journal of neuroscience research 1998;53(5):542-50.
1998: Stefano Carenini; Melitta Schachner; Rudolf Martini
Cytochalasin D disrupts the restricted localization of N-CAM, but not of L1, at sites of Schwann cell-neurite and Schwann cell-Schwann cell contact in culture.
Journal of neurocytology 1998;27(6):453-8.
1998: Rudolf Martini; Stefano Carenini
Formation and maintenance of the myelin sheath in the peripheral nerve: roles of cell adhesion molecules and the gap junction protein connexin 32.
Microscopy research and technique 1998;41(5):403-15.
1998: Rudolf Martini
Introduction to myelin formation and maintenance.
Microscopy research and technique 1998;41(5):341-3.
1998: Stefano Carenini; Dirk Montag; Melitta Schachner; Rudolf Martini
MAG-deficient Schwann cells myelinate dorsal root ganglion neurons in culture.
Glia 1998;22(3):213-20.
1997: M Dahme; Udo Bartsch; Rudolf Martini; B Anliker; Melitta Schachner; Ned Mantei
Disruption of the mouse L1 gene leads to malformations of the nervous system.
Nature genetics 1997;17(3):346-9.
1997: Rudolf Martini
Animal models for inherited peripheral neuropathies.
Journal of anatomy 1997;191 ( Pt 3)():321-36.
1997: P Anzini; DH Neuberg; Melitta Schachner; E Nelles; K Willecke; Jürgen Zielasek; Klaus V Toyka; Ueli Suter; Rudolf Martini
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1997;17(12):4545-51.
1997: Rudolf Martini; Melitta Schachner
Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules.
Glia 1997;19(4):298-310.
1997: Stefano Carenini; Dirk Montag; H Cremer; Melitta Schachner; Rudolf Martini
Absence of the myelin-associated glycoprotein (MAG) and the neural cell adhesion molecule (N-CAM) interferes with the maintenance, but not with the formation of peripheral myelin.
Cell and tissue research 1997;287(1):3-9.
1996: V Guénard; Dirk Montag; Melitta Schachner; Rudolf Martini
Onion bulb cells in mice deficient for myelin genes share molecular properties with immature, differentiated non-myelinating, and denervated Schwann cells.
Glia 1996;18(1):27-38.
1996: Josef Magyar; Rudolf Martini; T Ruelicke; Adriano Aguzzi; K Adlkofer; Z Dembic; Jürgen Zielasek; Klaus V Toyka; Ueli Suter
Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1996;16(17):5351-60.
1996: Jürgen Zielasek; Rudolf Martini; Klaus V Toyka
Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations.
Muscle & nerve 1996;19(8):946-52.
1996: M Schäfer; M Fruttiger; Dirk Montag; Melitta Schachner; Rudolf Martini
Disruption of the gene for the myelin-associated glycoprotein improves axonal regrowth along myelin in C57BL/Wlds mice.
Neuron 1996;16(6):1107-13.
1995: Rudolf Martini; Jürgen Zielasek; Klaus V Toyka; peter giese; Melitta Schachner
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
Nature genetics 1995;11(3):281-6.
1995: K Adlkofer; Rudolf Martini; Adriano Aguzzi; Jürgen Zielasek; Klaus V Toyka; Ueli Suter
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.
Nature genetics 1995;11(3):274-80.
1995: Rudolf Martini; M H Mohajeri; S Kasper; peter giese; Melitta Schachner
Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1995;15(6):4488-95.
1995: Karl-Heinz Braunewell; Rudolf Martini; Richard G LeBaron; H Kresse; Andreas Faissner; Brigitte Schmitz; Melitta Schachner
Up-regulation of a chondroitin sulphate epitope during regeneration of mouse sciatic nerve: evidence that the immunoreactive molecules are related to the chondroitin sulphate proteoglycans decorin and versican.
The European journal of neuroscience 1995;7(4):792-804.
1995: Melitta Schachner; Rudolf Martini
Glycans and the modulation of neural-recognition molecule function.
Trends in neurosciences 1995;18(4):183-91.
1995: M Fruttiger; Dirk Montag; Melitta Schachner; Rudolf Martini
Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity.
The European journal of neuroscience 1995;7(3):511-5.
1995: Melitta Schachner; Rudolf Martini; Heike Hall; G Orberger
Functions of the L2/HNK-1 carbohydrate in the nervous system.
Progress in brain research 1995;105():183-8.
1995: M Fruttiger; Melitta Schachner; Rudolf Martini
Tenascin-C expression during wallerian degeneration in C57BL/Wlds mice: possible implications for axonal regeneration.
Journal of neurocytology 1995;24(1):1-14.
1994: K Löw; G Orberger; Brigitte Schmitz; Rudolf Martini; Melitta Schachner
The L2/HNK-1 carbohydrate is carried by the myelin associated glycoprotein and sulphated glucuronyl glycolipids in muscle but not cutaneous nerves of adult mice.
The European journal of neuroscience 1994;6(12):1773-81.
1994: Rudolf Martini; Melitta Schachner; Thomas M Brushart
The L2/HNK-1 carbohydrate is preferentially expressed by previously motor axon-associated Schwann cells in reinnervated peripheral nerves.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1994;14(11 Pt 2):7180-91.
1994: Dirk Montag; peter giese; Udo Bartsch; Rudolf Martini; Y Lang; H Blüthmann; J Karthigasan; Daniel A Kirschner; E S Wintergerst; K A Nave
Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.
Neuron 1994;13(1):229-46.
1994: Rudolf Martini
Myelin-associated glycoprotein is not detectable in perikaryal myelin of spiral ganglion neurons of adult mice.
Glia 1994;10(4):311-4.
1994: Rudolf Martini; Y Xin; Melitta Schachner
Restricted localization of L1 and N-CAM at sites of contact between Schwann cells and neurites in culture.
Glia 1994;10(1):70-4.
1994: Rudolf Martini
Expression and functional roles of neural cell surface molecules and extracellular matrix components during development and regeneration of peripheral nerves.
Journal of neurocytology 1994;23(1):1-28.
1992: peter giese; Rudolf Martini; G Lemke; P Soriano; Melitta Schachner
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
Cell 1992;71(4):565-76.