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English
Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations
scientific article published on 01 August 1996
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
title
Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
author
Rudolf Martini
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
author name string
J Zielasek
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
K V Toyka
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
publication date
1 August 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
published in
Muscle and Nerve
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
page(s)
946-952
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
cites work
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Charcot-Marie-Tooth syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Congenital absence of peripheral myelin: abnormal Schwann cell development causes lethal arthrogryposis multiplex congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
CHANGES IN NERVE CONDUCTION IN EXPERIMENTAL ALLERGIC NEURITIS.
1 reference
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Crossref
reference URL
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retrieved
21 January 2018
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/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins
1 reference
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retrieved
21 January 2018
The role of macrophages and eicosanoids in the pathogenesis of experimental allergic neuritis. Serial clinical, electrophysiological, biochemical and morphological observations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Conduction failure and nerve conduction slowing in experimental allergic neuritis induced by P2-specific T-cell lines
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Charcot-Marie-Tooth neuropathies: from clinical description to molecular genetics
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21 January 2018
Hereditary demyelinating neuropathy in the Trembler mouse
1 reference
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21 January 2018
Refractory period, conduction of trains of impulses, and effect of temperature on conduction in chronic hypertrophic neuropathy
1 reference
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retrieved
21 January 2018
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
1 reference
stated in
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reference URL
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21 January 2018
Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.
1 reference
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Crossref
reference URL
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21 January 2018
Nerve grafts in the Trembler mouse. An electrophysiological and histological study
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retrieved
21 January 2018
Hypomyelination neuropathy in a female newborn presenting as arthrogryposis multiplex congenita.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Relation of clinical, serological, morphological, and electrophysiological findings in galactocerebroside-induced experimental allergic neuritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Peripheral myelin protein 22: facts and hypotheses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28199608%2919%3A8%3C946%3A%3AAID-MUS2%3E3.0.CO%3B2-8
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1097-4598(199608)19:8<946::AID-MUS2>3.0.CO;2-8
0 references
PubMed ID
8756159
1 reference
stated in
Europe PubMed Central
PubMed ID
8756159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8756159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
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