(Q77779360)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883862%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease (English)

1 reference

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8 December 2019

author name string

P Sindou

1

1 reference

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8 December 2019

J M Vallat

2

1 reference

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8 December 2019

F Chapon

3

1 reference

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8 December 2019

J J Archelos

4

1 reference

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8 December 2019

F Tabaraud

5

1 reference

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8 December 2019

T Anani

6

1 reference

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8 December 2019

K G Braund

7

1 reference

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8 December 2019

T Maisonobe

8

1 reference

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8 December 2019

J J Hauw

9

1 reference

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8 December 2019

A Vandenberghe

10

1 reference

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8 December 2019

publication date

1 January 1999

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8 December 2019

1 reference

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8 December 2019

volume

22

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8 December 2019

issue

1

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8 December 2019

page(s)

99-104

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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

8 December 2019

cites work

1 reference

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Production and characterization of monoclonal antibodies to the extracellular domain of P0.

21 January 2018

1 reference

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Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study

21 January 2018

1 reference

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Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po

21 January 2018

1 reference

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Role of myelin Po protein as a homophilic adhesion molecule

21 January 2018

1 reference

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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease

21 January 2018

1 reference

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

21 January 2018

1 reference

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Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin

21 January 2018

1 reference

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

21 January 2018

1 reference

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A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B

21 January 2018

1 reference

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Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region

21 January 2018

1 reference

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Isolation and analysis of the gene encoding peripheral myelin protein zero

21 January 2018

1 reference

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The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

21 January 2018

1 reference

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Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies

21 January 2018

1 reference

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Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene

21 January 2018

1 reference

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Recombinant peripheral myelin protein Po confers both adhesion and neurite outgrowth-promoting properties

21 January 2018

1 reference

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Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Biology and Genetics of Hereditary Motor and Sensory Neuropathies

21 January 2018

1 reference

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A technique for ultracryotomy of cell suspensions and tissues

21 January 2018

1 reference

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Ultrastructural PMP22 expression in inherited demyelinating neuropathies

21 January 2018

1 reference

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Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

21 January 2018

1 reference

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The immunoglobulin superfamily--domains for cell surface recognition

21 January 2018

1 reference

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10.1002/(SICI)1097-4598(199901)22:1<99::AID-MUS14>3.0.CO;2-5

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883862%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference