Many facets of the peripheral myelin protein PMP22 in myelination and disease (Q47808553)

5 February 2018

review article

1 reference

title

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

1 reference

5 February 2018

1 reference

Naef R

1

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5 February 2018

Suter U

series ordinal

2

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5 February 2018

publication date

1 June 1998

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5 February 2018

Microscopy Research and Technique

published in

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5 February 2018

volume

41

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5 February 2018

issue

5

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5 February 2018

page(s)

359-371

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5 February 2018

Abnormal myelination in transplanted Trembler mouse Schwann cells

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Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination

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

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

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Distribution of P0 protein and the myelin-associated glycoprotein in peripheral nerves from Trembler mice

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

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Sex-dependent rearrangements resulting in CMT1A and HNPP.

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Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

21 January 2018

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Animal models for inherited peripheral neuropathies.

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Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

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

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

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An in-frame deletion in peripheral myelin protein-22 gene causes hypomyelination and cell death of the schwann cells in the new Trembler mutant mice

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Trembler mouse carries a point mutation in a myelin gene

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Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

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A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

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Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis

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Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

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10.1002/(SICI)1097-0029(19980601)41:5<359::AID-JEMT3>3.0.CO;2-L

21 January 2018

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DOI

1 reference

5 February 2018

1 reference

5 February 2018