Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22 (Q73807766)

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6 November 2019

title

Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22 (English)

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6 November 2019

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S Niemann

1

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6 November 2019

M W Sereda

2

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6 November 2019

U Suter

3

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6 November 2019

I R Griffiths

4

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6 November 2019

K A Nave

5

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6 November 2019

publication date

1 June 2000

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6 November 2019

published in

Journal of Neuroscience

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6 November 2019

volume

20

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6 November 2019

issue

11

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6 November 2019

page(s)

4120-4128

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Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.

6 November 2019

cites work

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A growth arrest-specific (gas) gene codes for a membrane protein

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DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

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Myelin glycolipids and their functions

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Distal axonopathy in peripheral nerves of PMP22-mutant mice.

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The glycoprotein P0 in peripheral gliogenesis

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A gene encoding a protein with zinc fingers is activated during G0/G1 transition in cultured cells

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Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy.

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Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies

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P0 and PMP22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-beta family factors.

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Myelin formation in the sciatic nerve of the rat. A quantitative electron microscopic, histochemical and radioautographic study

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Schwann cell development, differentiation and myelination

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Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin

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12 December 2020

Many facets of the peripheral myelin protein PMP22 in myelination and disease.

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Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22.

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Assembly of asparagine-linked oligosaccharides

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Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A.

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Characterization of cloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice

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Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models

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Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)

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Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies

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Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

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Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy.

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New perspectives on the function of myelin galactolipids.

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12 December 2020

Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons.

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12 December 2020

Schwann cell differentiation

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12 December 2020

Characterization of peripheral myelin protein 22 in zebrafish (zPMP22) suggests an early role in the development of the peripheral nervous system

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12 December 2020

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

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12 December 2020

Krox-20 controls myelination in the peripheral nervous system

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12 December 2020

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

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12 December 2020

Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice

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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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12 December 2020

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

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12 December 2020

Gene transfer and molecular cloning of the rat nerve growth factor receptor

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12 December 2020

Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.

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12 December 2020

Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.

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12 December 2020

Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene

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12 December 2020

A transgenic rat model of Charcot-Marie-Tooth disease

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12 December 2020

Axons regulate Schwann cell expression of the major myelin and NGF receptor genes

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12 December 2020

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

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12 December 2020

Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

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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

The POU factor Oct-6 and Schwann cell differentiation

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12 December 2020

A myelin protein is encoded by the homologue of a growth arrest-specific gene

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12 December 2020

Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development

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12 December 2020

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages.

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12 December 2020

Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene

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12 December 2020

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

1 reference

12 December 2020

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

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12 December 2020

Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy

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12 December 2020

Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction

1 reference

12 December 2020

Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration

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12 December 2020

Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: modulation of cell growth

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12 December 2020

SCIP: a glial POU domain gene regulated by cyclic AMP.

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12 December 2020

Expression and activity of the POU transcription factor SCIP

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12 December 2020

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

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12 December 2020

Trembler mouse carries a point mutation in a myelin gene

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12 December 2020

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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12 December 2020

Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele

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12 December 2020

10.1523/JNEUROSCI.20-11-04120.2000

Identifiers

DOI

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6 November 2019

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6 November 2019

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