(Q44368294)

2 December 2017

title

Overexpression of the CT GalNAc transferase inhibits muscular dystrophy in a cleavage-resistant dystroglycan mutant mouse (English)

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2 December 2017

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Vianney Jayasinha

1

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2 December 2017

Kwame Hoyte

series ordinal

2

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2 December 2017

Bing Xia

series ordinal

3

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2 December 2017

Paul T Martin

series ordinal

4

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2 December 2017

language of work or name

English

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publication date

1 March 2003

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Biochemical and Biophysical Research Communications

2 December 2017

published in

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2 December 2017

volume

302

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2 December 2017

issue

4

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2 December 2017

page(s)

831-836

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Dystroglycan inside and out.

2 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

Inhibition of dystroglycan cleavage causes muscular dystrophy in transgenic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

Overexpression of the CT GalNAc transferase in skeletal muscle alters myofiber growth, neuromuscular structure, and laminin expression.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900271-7

10.1016/S0006-291X(03)00271-7

7 January 2021

Identifiers

DOI

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2 December 2017

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