Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse (Q41456452)

30 September 2017

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title

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse (English)

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congenital muscular dystrophy

30 September 2017

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Matsumura K

1

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30 September 2017

Yamada H

2

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30 September 2017

Saito F

3

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30 September 2017

Sunada Y

4

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30 September 2017

Shimizu T

5

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30 September 2017

1 January 1997

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30 September 2017

Neuromuscular Disorders

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30 September 2017

7

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30 September 2017

1

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30 September 2017

7-12

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Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

30 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy

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https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Dystrophin-associated proteins in muscular dystrophy

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https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

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/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

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https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

A new nomenclature for the laminins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Genetically determined defect of Schwann cell basement membrane in dystrophic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Quantitative studies of the abnormal axon-Schwann cell relationship in the peripheral motor and sensory nerves of the dystrophic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Conduction of nervous impulses in spinal roots and peripheral nerves of dystrophic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Electrophysiological properties of spinal motoneurones of normal and dystrophic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Characterization of dp6troglycan-laminin interaction in peripheral nerve.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

An alternative dystrophin transcript specific to peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Glycans and the modulation of neural-recognition molecule function.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

The agrin gene codes for a family of basal lamina proteins that differ in function and distribution

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Building synapses: agrin and dystroglycan stick together

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

The basement membrane at the neuromuscular junction: a synaptic mediatrix

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

SH3 domain-mediated interaction of dystroglycan and Grb2

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Axonal regulation of Schwann cell integrin expression suggests a role for alpha 6 beta 4 in myelination.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Differentiation of axon-related Schwann cells in vitro: II. Control of myelin formation by basal lamina.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Merosin promotes neurite growth and Schwann cell migration in vitro and nerve regeneration in vivo: evidence using an antibody to merosin, ARM-1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

Addition of purified basal lamina molecules enables Schwann cell ensheathment of sympathetic neurites in culture

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900402-6

7 January 2021

10.1016/S0960-8966(96)00402-6

Identifiers

DOI

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30 September 2017

1 reference