(Q48047021)

English

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

scientific article published in August 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

0 references

author name string

Suh JG

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Ichihara N

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Saigoh K

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Nakabayashi O

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Yamanishi T

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Tanaka K

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Wada K

7

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Kikuchi T

8

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

language of work or name

0 references

publication date

1 August 1997

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

79

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

735-744

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

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DNA deletion associated with hereditary neuropathy with liability to pressure palsies

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7 January 2021

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

1 reference

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Hereditary demyelinating motor and sensory neuropathy

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

1 reference

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7 January 2021

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From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins

1 reference

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7 January 2021

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Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination

1 reference

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Long lives for homozygous trembler mutant mice despite virtual absence of peripheral nerve myelin

1 reference

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Aberrant splicing of proteolipid protein mRNA in the dysmyelinating jimpy mutant mouse

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Axonal degeneration promotes abnormal accumulation of amyloid beta-protein in ascending gracile tract of gracile axonal dystrophy (GAD) mouse

1 reference

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7 January 2021

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Cell kinetics and cell death in the optic nerve of the myelin deficient rat

1 reference

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7 January 2021

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Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

1 reference

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7 January 2021

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Hereditary hypertrophic neuropathy in the trembler mouse. Part 2. Histopathological studies: electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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Identification of a 5' splice site mutation in the PMP-22 gene in autosomal dominant Charcot-Marie-Tooth disease type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

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Charcot-Marie-Tooth disease type 1A: mutational mechanisms and candidate gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Arrest of proteolipid transport through the Golgi apparatus in Jimpy brain

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

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A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

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Programmed cell death in the dysmyelinating mutants

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

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Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

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7 January 2021

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MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM

1 reference

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7 January 2021

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Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope

1 reference

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

1 reference

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7 January 2021

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Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5

1 reference

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7 January 2021

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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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900692-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Trembler mouse carries a point mutation in a myelin gene

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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Peripheral myelin protein 22: facts and hypotheses

1 reference

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

1 reference

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

1 reference

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Identifiers

10.1016/S0306-4522(96)00692-6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

release_tj23osso6nctbdw2kdhga355fy

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/9219937

ResearchGate publication ID

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