(Q73448132)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1B (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

N Tachi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

N Kozuka

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

K Ohya

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

S Chiba

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

K Sasaki

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

K Uyemura

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

publication date

1 January 2001

1 reference

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4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

33-35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

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

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

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/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

Isolation and analysis of the gene encoding peripheral myelin protein zero

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

Molecular and pathological studies in Charcot-Marie-Tooth disease 1A.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

A new mutation of the Po gene in patients with Charcot-Marie-Tooth disease type 1B: screening of the Po gene by heteroduplex analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

Expression of Po protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

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/10.1016%2FS0887-8994%2800%2900225-3

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/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

Myelin genes: getting the dosage right

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900225-3

7 January 2021

10.1016/S0887-8994(00)00225-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11182278%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference