(Q71794005)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

main subject

peripheral neuropathy

1 reference

2

1 reference

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21 October 2019

author name string

Adlkofer K

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Aguzzi A

3

1 reference

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21 October 2019

Zielasek J

4

1 reference

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21 October 2019

Toyka KV

5

1 reference

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21 October 2019

Suter U

6

1 reference

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21 October 2019

publication date

1 November 1995

1 reference

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21 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

11

1 reference

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21 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

274-280

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng1195-274

21 October 2019

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Neurological mouse mutants and the genes of myelin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Peripheral myelin protein 22: facts and hypotheses

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Trembler mouse carries a point mutation in a myelin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Hereditary neuropathy with liability to pressure palsies. Report of two families and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Morphometric analysis of normal, mutant, and transgenic CNS: correlation of myelin basic protein expression to myelinogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Abnormal myelination in transplanted Trembler mouse Schwann cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

The role of oligodendrocytes and myelin on axon maturation in the developing rat retinofugal pathway.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Refractory period, conduction of trains of impulses, and effect of temperature on conduction in chronic hypertrophic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Induction of type I interferon genes and interferon-inducible genes in embryonal stem cells devoid of interferon regulatory factor 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-274

7 January 2021

Identifiers

DOI

10.1038/NG1195-274

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581450%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference