(Q28569678)

31 January 2017

title

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A (English)

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31 January 2017

L. Nobbio

1

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31 January 2017

G. Mancardi

2

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31 January 2017

M. Grandis

3

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31 January 2017

G. Levi

4

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31 January 2017

U. Suter

5

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31 January 2017

K. A. Nave

6

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31 January 2017

A. J. Windebank

7

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31 January 2017

M. Abbruzzese

8

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31 January 2017

A. Schenone

9

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31 January 2017

publication date

1 July 2001

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31 January 2017

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31 January 2017

volume

50

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31 January 2017

issue

1

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31 January 2017

page(s)

47–55

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

31 January 2017

cites work

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A light and electron microscope study of long-term organized cultures of rat dorsal root ganglia

21 January 2018

1 reference

Abnormalities expressed in long-term cultures of dorsal root ganglia from the dystrophic mouse

21 January 2018

1 reference

Studies on the effects of altered PMP22 expression during myelination in vitro

21 January 2018

1 reference

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

21 January 2018

1 reference

Abnormal myelination in transplanted Trembler mouse Schwann cells

21 January 2018

1 reference

Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice.

21 January 2018

1 reference

PMP22 accumulation in aggresomes: implications for CMT1A pathology

21 January 2018

1 reference

Isolation and analysis of the gene encoding peripheral myelin protein zero

21 January 2018

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Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

21 January 2018

1 reference

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

21 January 2018

1 reference

Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies

21 January 2018

1 reference

Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

21 January 2018

1 reference

A transgenic rat model of Charcot-Marie-Tooth disease

21 January 2018

1 reference

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

21 January 2018

1 reference

Expression of the trembler mouse mutation in organotypic cultures of dorsal root ganglia.

21 January 2018

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

21 January 2018

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Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22

21 January 2018

1 reference

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

21 January 2018

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Congenital hypomyelination due to myelin protein zero Q215X mutation

21 January 2018

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Morphometric and freeze-fracture studies on peripheral nerve in shiverer mice

21 January 2018

1 reference

Myelin membrane structure and composition correlated: a phylogenetic study

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.1034

0 references

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