Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q35006513)
Watch
English
Mouse models of Charcot-Marie-Tooth disease.
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Mouse models of Charcot-Marie-Tooth disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
author
Yosuke Tanaka
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
author name string
Nobutaka Hirokawa
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
publication date
1 December 2002
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
volume
18
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
issue
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
page(s)
S39-44
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
cites work
Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trembler mouse carries a point mutation in a myelin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of myelin proteins in the adult heterozygous Trembler mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A transgenic rat model of Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations in X-linked Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Krox-20 controls myelination in the peripheral nervous system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities in the axonal cytoskeleton induced by a connexin32 mutation in nerve xenografts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Kinesin and dynein superfamily proteins and the mechanism of organelle transport
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
All kinesin superfamily protein, KIF, genes in mouse and human
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene targeting studies begin to reveal the function of neurofilament proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Delayed maturation of regenerating myelinated axons in mice lacking neurofilaments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The many faces of Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted integration of DNA using mutant lox sites in embryonic stem cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2902839-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(02)02839-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
PubMed publication ID
12446157
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12446157
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12446157%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit