(Q42524150)

1 November 2017

title

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

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1 November 2017

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8

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1 November 2017

11

Volker Straub

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1 November 2017

Katherine D Mathews

12

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Steven A Moore

object named as

Steven A Moore

13

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Kevin P Campbell

object named as

Kevin P Campbell

14

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author name string

Daniel E Michele

1

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1 November 2017

Rita Barresi

2

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1 November 2017

Motoi Kanagawa

3

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1 November 2017

Fumiaki Saito

4

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1 November 2017

Ronald D Cohn

5

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1 November 2017

Jakob S Satz

6

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1 November 2017

James Dollar

7

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1 November 2017

Richard I Kelley

9

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1 November 2017

Hannu Somer

10

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1 November 2017

language of work or name

English

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publication date

1 July 2002

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1 November 2017

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1 November 2017

volume

418

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1 November 2017

issue

6896

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1 November 2017

page(s)

417-422

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Congenital muscular dystrophy: an expanding clinical syndrome

1 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

The Fukuyama congenital muscular dystrophy story

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https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Dystroglycan inside and out.

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https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

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https://api.crossref.org/works/10.1038%2FNATURE00837

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/10.1038%2FNATURE00837

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

A role for dystroglycan in basement membrane assembly

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

A stoichiometric complex of neurexins and dystroglycan in brain

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Muscle-eye-brain disease: a neuropathological study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

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/10.1038%2FNATURE00837

7 January 2021

Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Congenital lymphocytic choriomeningitis virus infection: decade of rediscovery

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Mapping of domains in human laminin using monoclonal antibodies: localization of the neurite-promoting site

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00837

7 January 2021

Identifiers

DOI

10.1038/NATURE00837

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Dimensions Publication ID

1 November 2017

1012382376

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1 reference