The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22. (Q33787362)

29 July 2017

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title

The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22. (English)

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29 July 2017

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peripheral neuropathy

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Niemann S

1

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Sereda MW

2

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Rossner M

3

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Stewart H

4

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Suter U

5

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Meinck HM

6

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Griffiths IR

7

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Nave KA

8

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language of work or name

English

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publication date

1 September 1999

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Annals of the New York Academy of Sciences

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published in

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volume

883

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page(s)

254-261

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

29 July 2017

cites work

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Charcot-Marie-Tooth neuropathies: from clinical description to molecular genetics

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Trembler mouse carries a point mutation in a myelin gene

21 January 2018

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

21 January 2018

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

21 January 2018

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Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

21 January 2018

1 reference

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

21 January 2018

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10.1111/J.1749-6632.1999.TB08587.X

21 January 2018

Identifiers

DOI

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29 July 2017

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