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Muscular dystrophy--reason for optimism?
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Muscular dystrophy--reason for optimism?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
author
Kay Davies
series ordinal
2
object named as
Kay E Davies
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
author name string
Edward A Burton
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
language of work or name
English
0 references
publication date
1 January 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
published in
Cell
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
volume
108
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
page(s)
5-8
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
cites work
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Making sense of the limb-girdle muscular dystrophies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
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inferred from DOI database lookup
Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear envelope proteins and associated diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biomedicine. Reconstructing myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0092-8674(01)00626-2
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
PubMed ID
11792315
1 reference
stated in
Europe PubMed Central
PubMed ID
11792315
retrieved
2 August 2017
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