Fukuyama-type congenital muscular dystrophy: close relation between changes in the muscle basal lamina and plasma membrane (Q42479480)

1 November 2017

title

Fukuyama-type congenital muscular dystrophy: close relation between changes in the muscle basal lamina and plasma membrane (English)

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congenital muscular dystrophy

1 November 2017

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Matsubara S

1

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1 November 2017

Mizuno Y

2

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1 November 2017

Kitaguchi T

3

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1 November 2017

Isozaki E

4

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1 November 2017

Miyamoto K

5

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1 November 2017

Hirai S

6

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1 November 2017

publication date

1 October 1999

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1 November 2017

published in

Neuromuscular Disorders

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1 November 2017

volume

9

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1 November 2017

issue

6-7

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1 November 2017

page(s)

388-398

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Abnormal localization of laminin subunits in muscular dystrophies

1 November 2017

cites work

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Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

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Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

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7 January 2021

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

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7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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7 January 2021

Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

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https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900049-8

7 January 2021

Basement membrane abnormality in merosin-negative congenital muscular dystrophy

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7 January 2021

Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy

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7 January 2021

Presence of Laminin 5 Chain and Lack of Laminin 1 Chain during Human Muscle Development and in Muscular Dystrophies

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7 January 2021

Immunogold and freeze etch electron microscopic studies of merosin localization in basal lamina of human skeletal muscle fibers

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https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900049-8

7 January 2021

Mutations in the integrin alpha7 gene cause congenital myopathy

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

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7 January 2021

Expression of laminin subunits in congenital muscular dystrophy

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Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

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7 January 2021

Dystrophin-associated glycoprotein and dystrophin co-localisation at sarcolemma in Fukuyama congenital muscular dystrophy

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7 January 2021

Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

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https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900049-8

7 January 2021

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

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7 January 2021

Ultrastructural changes in polymyositis

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7 January 2021

10.1016/S0960-8966(99)00049-8

Identifiers

DOI

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1 November 2017

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