(Q35006513)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

review article

1 reference

title

Mouse models of Charcot-Marie-Tooth disease (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

author name string

Nobutaka Hirokawa

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

publication date

1 December 2002

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

issue

12

1 reference

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15 December 2019

page(s)

S39-44

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Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies.

15 December 2019

cites work

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients

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7 January 2021

Trembler mouse carries a point mutation in a myelin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Expression of myelin proteins in the adult heterozygous Trembler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

1 reference

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7 January 2021

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

1 reference

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7 January 2021

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

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7 January 2021

Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

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%2FS0168-9525%2802%2902839-1

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%2FS0168-9525%2802%2902839-1

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%2FS0168-9525%2802%2902839-1

7 January 2021

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice

1 reference

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7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

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7 January 2021

Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Krox-20 controls myelination in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Abnormalities in the axonal cytoskeleton induced by a connexin32 mutation in nerve xenografts

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Kinesin and dynein superfamily proteins and the mechanism of organelle transport

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

All kinesin superfamily protein, KIF, genes in mouse and human

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Gene targeting studies begin to reveal the function of neurofilament proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Delayed maturation of regenerating myelinated axons in mice lacking neurofilaments

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

The many faces of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Targeted integration of DNA using mutant lox sites in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1

7 January 2021

10.1016/S0168-9525(02)02839-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference