(Q33787357)

29 July 2017

1 reference

title

Transgenic mouse models of CMT1A and HNPP. (English)

1 reference

29 July 2017

Suter U

1

1 reference

29 July 2017

Nave KA

series ordinal

2

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

Annals of the New York Academy of Sciences

29 July 2017

number of pages

7

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

29 July 2017

volume

883

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29 July 2017

page(s)

247-253

1 reference

Trembler mouse carries a point mutation in a myelin gene

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Fate of Schwann cells in CMT1A and HNPP: evidence for apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Influence of elevated expression of rat wild-type PMP22 and its mutant PMP22Trembler on cell growth of NIH3T3 fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

Animal models for inherited peripheral neuropathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08586.X

10.1111/J.1749-6632.1999.TB08586.X

21 January 2018

Identifiers

DOI

1 reference

release_2s6xuz2bdnaufjstjdvsm6ztre

29 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2s6xuz2bdnaufjstjdvsm6ztre

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference