(Q40606913)

22 September 2017

title

Disruption of dystroglycan axis by beta-dystroglycan processing in cardiomyopathic hamster muscle (English)

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22 September 2017

Kiichiro Matsumura

1

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22 September 2017

Ken Arai

2

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22 September 2017

Di Zhong

3

1 reference

22 September 2017

Fumiaki Saito

4

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22 September 2017

Hiroko Fukuta-Ohi

5

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22 September 2017

Ryuji Maekawa

6

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22 September 2017

Hiroki Yamada

7

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22 September 2017

Teruo Shimizu

8

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22 September 2017

publication date

1 December 2003

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22 September 2017

published in

Neuromuscular Disorders

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22 September 2017

volume

13

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22 September 2017

issue

10

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22 September 2017

page(s)

796-803

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

22 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Biosynthesis of dystroglycan: processing of a precursor propeptide

1 reference

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7 January 2021

The complexities of dystroglycan

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7 January 2021

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

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7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

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7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Structural and functional analysis of the N-terminal extracellular region of beta-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

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

1 reference

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7 January 2021

A role for dystroglycan in basement membrane assembly

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7 January 2021

Laminin polymerization induces a receptor-cytoskeleton network

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7 January 2021

Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation

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7 January 2021

Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycan complex.

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7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

1 reference

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7 January 2021

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

1 reference

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7 January 2021

Strain- and age-dependent loss of sarcoglycan complex in cardiomyopathic hamster hearts and its re-expression by delta-sarcoglycan gene transfer in vivo

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7 January 2021

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy

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7 January 2021

Dystroglycan in development and disease.

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7 January 2021

Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies

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7 January 2021

Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart

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7 January 2021

Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster

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7 January 2021

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer

1 reference

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7 January 2021

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

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7 January 2021

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

1 reference

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7 January 2021

Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

A role of dystroglycan in schwannoma cell adhesion to laminin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Multiplex Western blotting system for the analysis of muscular dystrophy proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Defective glycosylation in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

An ischemic beta-dystroglycan (betaDG) degradation product: correlation with irreversible injury in adult rabbit cardiomyocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

Dystroglycan expression is frequently reduced in human breast and colon cancers and is associated with tumor progression.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900139-1

7 January 2021

10.1016/S0960-8966(03)00139-1

Identifiers

DOI

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22 September 2017

1 reference