(Q34495023)

2 August 2017

1 reference

title

Muscular dystrophy--reason for optimism? (English)

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2 August 2017

2

Kay E Davies

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2 August 2017

Edward A Burton

1

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2 August 2017

language of work or name

English

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publication date

1 January 2002

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2 August 2017

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2 August 2017

volume

108

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2 August 2017

issue

1

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2 August 2017

page(s)

5-8

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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

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Making sense of the limb-girdle muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Nuclear envelope proteins and associated diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Biomedicine. Reconstructing myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

7 January 2021

Expression of full-length utrophin prevents muscular dystrophy in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900626-2

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/10.1016%2FS0092-8674%2801%2900626-2

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%2FS0092-8674%2801%2900626-2

7 January 2021

10.1016/S0092-8674(01)00626-2

Identifiers

DOI

1 reference

2 August 2017

1 reference