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Neuroinflammation in the peripheral nerve: Cause, modulator, or bystander in peripheral neuropathies?

Glia, 2016-04, Vol.64 (4), p.475-486

2016

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Neuroinflammation as modifier of genetically caused neurological disorders of the central nervous system: Understanding pathogenesis and chances for treatment

Glia, 2017-09, Vol.65 (9), p.1407-1422

2017

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Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease

Glia, 2008-11, Vol.56 (14), p.1566-1577

2008

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Macrophage Depletion Ameliorates Peripheral Neuropathy in Aging Mice

The Journal of neuroscience, 2018-05, Vol.38 (19), p.4610-4620

2018

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Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3193-3205

2015

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Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice

The Journal of neuroscience, 2016-02, Vol.36 (6), p.1890-1901

2016

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MCP-1/CCL2 Modifies Axon Properties in a PMP22-Overexpressing Mouse Model for Charcot-Marie-Tooth 1A Neuropathy

The American journal of pathology, 2010-03, Vol.176 (3), p.1390-1399

2010

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A Key Role for gp130 Expressed on Peripheral Sensory Nerves in Pathological Pain

The Journal of neuroscience, 2009-10, Vol.29 (43), p.13473-13483

2009

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Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking

Glia, 2016-01, Vol.64 (1), p.155-174

2016

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CNTF is a major protective factor in demyelinating CNS disease: A neurotrophic cytokine as modulator in neuroinflammation

Nature medicine, 2002-06, Vol.8 (6), p.620-624

2002

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Immune Cells Contribute to Myelin Degeneration and Axonopathic Changes in Mice Overexpressing Proteolipid Protein in Oligodendrocytes

The Journal of neuroscience, 2006-08, Vol.26 (31), p.8206-8216

2006

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Disruption of the mouse L1 gene leads to malformations of the nervous system

Nature genetics, 1997-11, Vol.17 (3), p.346-349

1997

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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

Nature genetics, 1995-11, Vol.11 (3), p.274-280

1995

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Glycans and the modulation of neural-recognition molecule function

Trends in Neurosciences, 1995-04, Vol.18 (4), p.183-191

1995

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Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32

The Journal of neuroscience, 1997-06, Vol.17 (12), p.4545-4551

1997

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P0 Glycoprotein Overexpression Causes Congenital Hypomyelination of Peripheral Nerves

The Journal of cell biology, 2000-03, Vol.148 (5), p.1021-1034

2000

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Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

Nature genetics, 1995-11, Vol.11 (3), p.281-286

1995

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Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules

Glia, 1997-04, Vol.19 (4), p.298-310

1997

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Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants

Molecular and cellular neuroscience, 2004-01, Vol.25 (1), p.83-94

2004

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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 neuroscience, 2008-08, Vol.38 (4), p.489-494

2008

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Mice deficient for the glycoprotein show subtle abnormalities in myelin

Neuron (Cambridge, Mass.), 1994-07, Vol.13 (1), p.229-246

1994

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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, 1999-10, Vol.883 (1), p.273-280

MARTINI, RUDOLF

1999

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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, 2004-05, Vol.165 (4), p.565-573

2004

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The effect of myelinating Schwann cells on axons

Muscle & nerve, 2001-04, Vol.24 (4), p.456-466

Martini, Rudolf

2001

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Neuroinflammation in the peripheral nerve: Cause, modulator, or bystander in peripheral neuropathies?

Neuroinflammation as modifier of genetically caused neurological disorders of the central nervous system: Understanding pathogenesis and chances for treatment

Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease

Macrophage Depletion Ameliorates Peripheral Neuropathy in Aging Mice

Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice

Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice

MCP-1/CCL2 Modifies Axon Properties in a PMP22-Overexpressing Mouse Model for Charcot-Marie-Tooth 1A Neuropathy

Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies

A Key Role for gp130 Expressed on Peripheral Sensory Nerves in Pathological Pain

Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking

CNTF is a major protective factor in demyelinating CNS disease: A neurotrophic cytokine as modulator in neuroinflammation

Immune Cells Contribute to Myelin Degeneration and Axonopathic Changes in Mice Overexpressing Proteolipid Protein in Oligodendrocytes

Disruption of the mouse L1 gene leads to malformations of the nervous system

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

Glycans and the modulation of neural-recognition molecule function

Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32

P0 Glycoprotein Overexpression Causes Congenital Hypomyelination of Peripheral Nerves

Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules

Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants

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

Mice deficient for the glycoprotein show subtle abnormalities in myelin

P0-Deficient Knockout Mice as Tools to Understand Pathomechanisms in Charcot-Marie-Tooth 1B and P0-Related Déjérine-Sottas Syndrome

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 effect of myelinating Schwann cells on axons

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