(Q71794009)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Karl Peter Giese

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

5

Schachner M

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

author name string

Zielasek J

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Toyka KV

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

publication date

1 November 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

281-286

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng1195-281

21 October 2019

exact match

0 references

cites work

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%2FNG1195-281

7 January 2021

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Mutation of the myelin P0 gene in Charcot-Marie-tooth neuropathy type 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

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%2FNG1195-281

7 January 2021

Imaging myelinated nerve fibres by confocal fluorescence microscopy: individual fibres in whole nerve trunks traced through multiple consecutive internodes

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Enhanced expression of the extracellular matrix molecule J1/tenascin in the regenerating adult mouse sciatic nerve

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Tenascin-C expression during wallerian degeneration in C57BL/Wlds mice: possible implications for axonal regeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Two cases of congenital hypomyelination neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

THE HYPERTROPHIC FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHY

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Expression of myelin protein gene transcripts by schwann cells of regenerating nerve

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

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%2FNG1195-281

7 January 2021

Neurological mouse mutants and the genes of myelin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

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%2FNG1195-281

7 January 2021

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Mutations in demyelinating peripheral neuropathies support molecular model of myelin P0-glycoprotein extracellular domain

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Tenascin promotes cerebellar granule cell migration and neurite outgrowth by different domains in the fibronectin type III repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

The role of macrophages and eicosanoids in the pathogenesis of experimental allergic neuritis. Serial clinical, electrophysiological, biochemical and morphological observations

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-281

7 January 2021

Identifiers

DOI

10.1038/NG1195-281

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference