Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance (Q73348017)

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3 November 2019

title

Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance (English)

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3 November 2019

author name string

C D Schmid

1

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3 November 2019

M Stienekemeier

2

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3 November 2019

S Oehen

3

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3 November 2019

F Bootz

4

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3 November 2019

J Zielasek

5

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3 November 2019

R Gold

6

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3 November 2019

K V Toyka

7

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3 November 2019

publication date

1 January 2000

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3 November 2019

published in

Journal of Neuroscience

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3 November 2019

volume

20

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3 November 2019

issue

2

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3 November 2019

page(s)

729-735

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Acute inflammatory neuropathy in Charcot-Marie-Tooth disease

3 November 2019

cites work

1 reference

12 December 2020

Molecular genetics of demyelination: new wrinkles on an old membrane

1 reference

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Heterogeneity of T-cell receptor usage in experimental autoimmune neuritis in the Lewis rat.

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Myelin Po protein mutated at Cys21 has a dominant-negative effect on adhesion of wild type Po.

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Expression of Schwann cell and peripheral T-cell activation epitopes in hereditary motor and sensory neuropathy

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Dominant-negative effect on adhesion by myelin Po protein truncated in its cytoplasmic domain

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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease

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12 December 2020

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

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12 December 2020

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

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12 December 2020

T lymphocyte recognition sites on peripheral nerve myelin P0 protein

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Lymphoid development in mice congenitally lacking T cell receptor alpha beta-expressing cells

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RAG-1-deficient mice have no mature B and T lymphocytes

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12 December 2020

Two subsets of rat T lymphocytes defined with monoclonal antibodies

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12 December 2020

T cell antigenic and neuritogenic activity of recombinant human peripheral myelin P2 protein

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12 December 2020

Animal models for inherited peripheral neuropathies.

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12 December 2020

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

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Myelin autoreactivity in multiple sclerosis: recognition of myelin basic protein in the context of HLA-DR2 products by T lymphocytes of multiple-sclerosis patients and healthy donors.

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Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination

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Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies

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Mechanisms of immune regulation in the peripheral nervous system.

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Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome

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Constitutive biological activity of thymus-independent TCR-alpha-beta+ intestinal intraepithelial lymphocytes in TCR-alpha-/- gene disruption mice.

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Suppression of experimental allergic encephalomyelitis in Lewis rats after elimination of macrophages

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Charcot-Marie-Tooth disease and related peripheral neuropathies

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Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice

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12 December 2020

Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyria

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12 December 2020

Inherited demyelinating neuropathies: from gene to disease

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12 December 2020

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

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12 December 2020

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

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12 December 2020

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

1 reference

12 December 2020

Control of myelin formation by axon caliber. (With a model of the control mechanism)

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12 December 2020

Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutation

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12 December 2020

Activated T cells in type I Charcot-Marie-Tooth disease: evidence for immunologic heterogeneity

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12 December 2020

Inflammatory infiltrates in sural nerve biopsies in Guillain-Barre syndrome and chronic inflammatory demyelinating neuropathy

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12 December 2020

Cell adhesion molecules of the immunoglobulin supergene family as tissue-specific autoantigens: induction of experimental allergic neuritis (EAN) by P0 protein-specific T cell lines

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12 December 2020

Therapy with monoclonal antibodies by elimination of T-cell subsets in vivo

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12 December 2020

Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP)

1 reference

12 December 2020

Selective elimination of macrophages by dichlormethylene diphosphonate-containing liposomes suppresses experimental autoimmune neuritis

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12 December 2020

Myelin genes: getting the dosage right

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12 December 2020

F4/80, a monoclonal antibody directed specifically against the mouse macrophage

1 reference

12 December 2020

10.1523/JNEUROSCI.20-02-00729.2000

Identifiers

DOI

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3 November 2019

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3 November 2019

PubMed publication ID

10632602

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