(Q71848820)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8950710%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Inherited demyelinating peripheral neuropathies: relating myelin packing abnormalities to P0 molecular defects (English)

1 reference

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21 October 2019

1

1 reference

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21 October 2019

author name string

K Szumowski

2

1 reference

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21 October 2019

A A Gabreëls-Festen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8950710%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

J E Hoogendijk

4

1 reference

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21 October 2019

P A Bolhuis

5

1 reference

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21 October 2019

publication date

1 November 1996

1 reference

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Journal of Neuroscience Research

21 October 2019

published in

1 reference

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21 October 2019

volume

46

1 reference

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21 October 2019

issue

4

1 reference

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21 October 2019

page(s)

502-508

1 reference

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Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene

21 October 2019

cites work

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Folding and function of the myelin proteins from primary sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

Compact myelin exists in the absence of basic protein in the shiverer mutant mouse

21 January 2018

1 reference

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Processing for electron microscopy alters membrane structure and packing in myelin

21 January 2018

1 reference

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

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

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

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

Molecular genetics of Charcot-Marie-Tooth neuropathy

21 January 2018

1 reference

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Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

Adult polyglucosan body disease: Clinical and nerve biopsy findings in two cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

Myelin P0-glycoprotein: predicted structure and interactions of extracellular domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4547%2819961115%2946%3A4%3C502%3A%3AAID-JNR12%3E3.0.CO%3B2-%23

10.1002/(SICI)1097-4547(19961115)46:4<502::AID-JNR12>3.0.CO;2-#

21 January 2018

Identifiers

DOI

0 references

1 reference