Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function (Q33289428)

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title

Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function (English)

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Michael D Henry

8

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author name string

Motoi Kanagawa

1

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Daniel E Michele

2

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Jakob S Satz

3

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Rita Barresi

4

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Hajime Kusano

5

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Takako Sasaki

6

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Rupert Timpl

7

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Kevin P Campbell

9

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language of work or name

English

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publication date

1 August 2005

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volume

579

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issue

21

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page(s)

4792-4796

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Dystroglycan: important player in skeletal muscle and beyond

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cites work

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

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/10.1016%2FJ.FEBSLET.2005.07.059

Molecular recognition by LARGE is essential for expression of functional dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Characterization of recombinant perlecan domain I and its substitution by glycosaminoglycans and oligosaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

The C-terminal domain V of perlecan promotes beta1 integrin-mediated cell adhesion, binds heparin, nidogen and fibulin-2 and can be modified by glycosaminoglycans

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Laminin polymerization induces a receptor-cytoskeleton network

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

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/10.1016%2FJ.FEBSLET.2005.07.059

Form and function: the laminin family of heterotrimers

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Expression and function of laminins in the embryonic and mature vasculature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Laminin-6 assembles into multimolecular fibrillar complexes with perlecan and participates in mechanical-signal transduction via a dystroglycan-dependent, integrin-independent mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

Laminin-sulfatide binding initiates basement membrane assembly and enables receptor signaling in Schwann cells and fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.07.059

The N-terminal globular domain of the laminin alpha1 chain binds to alpha1beta1 and alpha2beta1 integrins and to the heparan sulfate-containing domains of perlecan

21 January 2018

1 reference

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10.1016/J.FEBSLET.2005.07.059

21 January 2018

Identifiers

DOI

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25 July 2017

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