(Q42479484)

1 November 2017

title

Distribution of ten laminin chains in dystrophic and regenerating muscles (English)

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1 November 2017

Patton BL

1

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1 November 2017

Connoll AM

2

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1 November 2017

Martin PT

3

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1 November 2017

Cunningham JM

4

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1 November 2017

Mehta S

5

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1 November 2017

Pestronk A

6

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1 November 2017

Miner JH

7

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1 November 2017

Sanes JR

8

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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)

423-433

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The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform

1 November 2017

cites work

1 reference

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7 January 2021

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Distribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunits

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7 January 2021

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

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7 January 2021

A new nomenclature for the laminins

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7 January 2021

Merosin and laminin in myogenesis; specific requirement for merosin in myotube stability and survival

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7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

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7 January 2021

Absence of integrin alpha 7 causes a novel form of muscular dystrophy

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7 January 2021

Mutations in the integrin alpha7 gene cause congenital myopathy

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Congenital muscular dystrophy: from rags to riches

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7 January 2021

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

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7 January 2021

Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

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7 January 2021

Abnormal localization of laminin subunits in muscular dystrophies

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7 January 2021

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Expression of laminin subunits in congenital muscular dystrophy

1 reference

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7 January 2021

Increased laminin A expression in regenerating myofibers in neuromuscular disorders

1 reference

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7 January 2021

Laminin 2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebroocular dysplasia-muscular dystrophy)

1 reference

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7 January 2021

Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining

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7 January 2021

Clinical heterogeneity of adhalin deficiency

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7 January 2021

Changes of laminin beta 2 chain expression in congenital muscular dystrophy

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Epiligrin, a new cell adhesion ligand for integrin alpha 3 beta 1 in epithelial basement membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Primary structure and expression of a novel human laminin alpha 4 chain

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Mutations in the sarcoglycan genes in patients with myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Three "myosin adenosine triphosphatase" systems: the nature of their pH lability and sulfhydryl dependence

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Primary structure of the human laminin A chain. Limited expression in human tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Neural Targeting of Mycobacterium leprae Mediated by the G Domain of the Laminin-α2 Chain

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Abscence of laminin alpha1 chain in the skeletal muscle of dystrophic dy/dy mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

A synaptic localization domain in the synaptic cleft protein laminin beta 2 (s-laminin)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Developmental regulation of the laminin alpha5 chain suggests a role in epithelial and endothelial cell maturation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Fetal myosin heavy chains in regenerating muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Regeneration in free grafts of normal and denervated muscles in the rat: Morphology and histochemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Fetal myosin immunoreactivity in human dystrophic muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900033-4

7 January 2021

10.1016/S0960-8966(99)00033-4

Identifiers

DOI

1 reference

1 November 2017

1 reference