Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28589172)
Watch
English
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
title
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
(English)
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
main subject
LARGE xylosyl- and glucuronyltransferase 1
1 reference
stated in
GOA release 2020-03-11
glycosylation
1 reference
based on heuristic
inferred from title
author name string
P. K. Grewal
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
P. J. Holzfeind
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
R. E. Bittner
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
J. E. Hewitt
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 June 2001
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
volume
28
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
page(s)
151–154
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
issue
2
1 reference
stated in
PubMed
PubMed ID
11381262
retrieved
31 January 2017
cites work
Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myodystrophy, a new myopathy on chromosome 8 of the mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mapping near the myd locus on mouse chromosome 8
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure/function studies of glycosyltransferases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis for structural diversity in the core regions of the lipopolysaccharides of Escherichia coli and Salmonella enterica
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystroglycan in development and disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Membrane organization of the dystrophin-glycoprotein complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
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/10.1038%2F88865
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/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fukutin protein family--predicted enzymes modifying cell-surface molecules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystroglycan is a binding protein of laminin and merosin in peripheral nerve
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F88865
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/88865
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1100394
OpenCitations bibliographic resource ID
1100394
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1100394
PubMed ID
11381262
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1100394
ResearchGate publication ID
11958158
0 references
Springer Nature article ID
10.1038/88865
0 references
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