(Q46986553)

27 December 2017

title

An extracellular pathway for dystroglycan function in acetylcholine receptor aggregation and laminin deposition in skeletal myotubes (English)

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27 December 2017

author name string

Mathieu R Tremblay

series ordinal

1

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27 December 2017

Salvatore Carbonetto

series ordinal

2

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27 December 2017

language of work or name

English

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publication date

10 March 2006

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27 December 2017

Journal of Biological Chemistry

published in

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27 December 2017

volume

281

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27 December 2017

issue

19

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27 December 2017

page(s)

13365-13373

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27 December 2017

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

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

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The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane

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Distribution and turnover rate of acetylcholine receptors throughout the junction folds at a vertebrate neuromuscular junction

21 January 2018

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Rate constants of acetylcholine receptor internalization and degradation in mouse muscles.

21 January 2018

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Distinct roles of nerve and muscle in postsynaptic differentiation of the neuromuscular synapse

21 January 2018

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Patterning of muscle acetylcholine receptor gene expression in the absence of motor innervation

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The postsynaptic 43k protein clusters muscle nicotinic acetylcholine receptors in xenopus oocytes

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Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex

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21 January 2018

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Agrin-induced phosphorylation of the acetylcholine receptor regulates cytoskeletal anchoring and clustering

21 January 2018

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Acetylcholinesterase clustering at the neuromuscular junction involves perlecan and dystroglycan

21 January 2018

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Absence of acetylcholinesterase at the neuromuscular junctions of perlecan-null mice

21 January 2018

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Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin binding

21 January 2018

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21 January 2018

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Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking alpha- and beta1-syntrophins

21 January 2018

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21 January 2018

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

21 January 2018

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The ability of agrin to cluster AChRs depends on alternative splicing and on cell surface proteoglycans

21 January 2018

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Mechanism of agrin-induced acetylcholine receptor aggregation

21 January 2018

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Former neuritic pathways containing endogenous neural agrin have high synaptogenic activity

21 January 2018

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Laminin-1 redistributes postsynaptic proteins and requires rapsyn, tyrosine phosphorylation, and Src and Fyn to stably cluster acetylcholine receptors

21 January 2018

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MuSK is required for anchoring acetylcholinesterase at the neuromuscular junction

21 January 2018

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A synaptic localization domain in the synaptic cleft protein laminin beta 2 (s-laminin)

21 January 2018

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Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin beta 2

21 January 2018

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Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice

21 January 2018

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21 January 2018

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21 January 2018

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Contributions of the LG modules and furin processing to laminin-2 functions

21 January 2018

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Dystroglycan inside and out.

21 January 2018

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Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

21 January 2018

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Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 January 2018

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Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

21 January 2018

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Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse

21 January 2018

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Molecular recognition by LARGE is essential for expression of functional dystroglycan

21 January 2018

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Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Dystroglycan glycosylation and its role in matrix binding in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

The effects of post-translational processing on dystroglycan synthesis and trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

The role of the SEA (sea urchin sperm protein, enterokinase and agrin) module in cleavage of membrane-tethered mucins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

The MUC1 SEA module is a self-cleaving domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

alpha-dystroglycan isoforms are differentially distributed in adult rat retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

beta-Dystroglycan can be revealed in microsomes from mdx mouse muscle by detergent treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Conjugation of LG domains of agrins and perlecan to polymerizing laminin-2 promotes acetylcholine receptor clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

A transmembrane protein required for acetylcholine receptor clustering in Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

The Ror receptor tyrosine kinase CAM-1 is required for ACR-16-mediated synaptic transmission at the C. elegans neuromuscular junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Disruption of the mouse Large gene in the enr and myd mutants results in nerve, muscle, and neuromuscular junction defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

SH3 domain-mediated interaction of dystroglycan and Grb2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Epitopes in the interacting regions of beta-dystroglycan (PPxY motif) and dystrophin (WW domain).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Not all perlecans are created equal: interactions with fibroblast growth factor (FGF) 2 and FGF receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Fibroblast growth factor-binding protein is a novel partner for perlecan protein core

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Neuregulins and erbB receptors at neuromuscular junctions and at agrin-induced postsynaptic-like apparatus in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Dystroglycan distribution in adult mouse brain: a light and electron microscopy study

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600912200

21 January 2018

Identifiers

DOI

10.1074/JBC.M600912200

1 reference

27 December 2017

PubMed ID

16531403

1 reference

27 December 2017