Defective glycosylation in muscular dystrophy (Q34992775)

5 August 2017

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title

Defective glycosylation in muscular dystrophy (English)

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5 August 2017

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5

Susan C Brown

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5 August 2017

1

Francesco Muntoni

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5 August 2017

Martin Brockington

2

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5 August 2017

Derek J Blake

series ordinal

3

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5 August 2017

Silvia Torelli

series ordinal

4

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5 August 2017

language of work or name

English

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publication date

1 November 2002

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5 August 2017

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5 August 2017

volume

360

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5 August 2017

issue

9343

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5 August 2017

page(s)

1419-1421

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

5 August 2017

1 reference

7 January 2021

Biological roles of oligosaccharides: all of the theories are correct

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Structures and functions of the sugar chains of glycoproteins

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

O-mannosyl glycans in mammals

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Concepts and principles of O-linked glycosylation

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Congenital disorders of glycosylation

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Dystroglycan inside and out.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

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%2FS0140-6736%2802%2911397-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

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%2FS0140-6736%2802%2911397-3

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%2FS0140-6736%2802%2911397-3

7 January 2021

Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Muscle-eye-brain disease: a neuropathological study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency

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https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Mutations in the rotated abdomen locus affect muscle development and reveal an intrinsic asymmetry in Drosophila.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

Association of a missense mutation of the laminin alpha2 gene with tuberculoid type of leprosy in Indonesian patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2911397-3

7 January 2021

10.1016/S0140-6736(02)11397-3

Identifiers

DOI

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5 August 2017

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