Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses (Q28141198)

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scientific article (publication date: November 1999)

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English	Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses	scientific article (publication date: November 1999)

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instance of

scholarly article

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title

Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses (English)

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main subject

muscular dystrophy

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based on heuristic

inferred from title

author name string

P D Côté

series ordinal

1

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H Moukhles

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2

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M Lindenbaum

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3

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S Carbonetto

series ordinal

4

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language of work or name

English

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publication date

November 1999

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published in

Nature Genetics

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volume

23

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issue

3

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page(s)

338-42

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cites work

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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The sarcoglycan complex in limb-girdle muscular dystrophy

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering.

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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A role for dystroglycan in basement membrane assembly

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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inferred from DOI database lookup

Laminin polymerization induces a receptor-cytoskeleton network

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F15519

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Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Skeletal and Cardiac Myopathies in Mice Lacking Utrophin and Dystrophin: A Model for Duchenne Muscular Dystrophy

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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A technique for detection and relative quantitative analysis of glucosephosphate isomerase isozymes from nanogram tissue samples

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Cranin: a laminin-binding protein of cell membranes

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Dystroglycan binds nerve and muscle agrin

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

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Acetylcholinesterase clustering at the neuromuscular junction involves perlecan and dystroglycan

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Forced expression of dystrophin deletion constructs reveals structure-function correlations.

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

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Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

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alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F15519

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Laminin and alpha-dystroglycan mediate acetylcholine receptor aggregation via a MuSK-independent pathway

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

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Evidence for in situ and in vitro association between beta-dystroglycan and the subsynaptic 43K rapsyn protein. Consequence for acetylcholine receptor clustering at the synapse

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of nicotinic acetylcholine receptor cluster formation by rapsyn

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Crossref

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

based on heuristic

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The formation of neuromuscular synapses

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES

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https://api.crossref.org/works/10.1038%2F15519

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7 January 2021

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Identifiers

DOI

10.1038/15519

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1100403

OpenCitations bibliographic resource ID

1100403

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1100403

PubMed publication ID

10610181

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1100403

ResearchGate publication ID

51356388

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