(Q40925883)

24 September 2017

title

Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles (English)

1 reference

24 September 2017

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Vilquin JT

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24 September 2017

Guérette B

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24 September 2017

Puymirat J

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24 September 2017

Yaffe D

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24 September 2017

Tomé FM

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24 September 2017

Fardeau M

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24 September 2017

Fiszman M

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24 September 2017

Schwartz K

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24 September 2017

Tremblay JP

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24 September 2017

language of work or name

1 reference

1 May 1999

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24 September 2017

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24 September 2017

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24 September 2017

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24 September 2017

page(s)

792-800

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Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development

24 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

A new nomenclature for the laminins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Distribution and Function of Laminins in the Neuromuscular System of Developing, Adult, and Mutant Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Disruption of the lama2 gene in embryonic stem cells: laminin alpha 2 is necessary for sustenance of mature muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Muscular dystrophy in the mouse caused by an allele at the dy-locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

SV40 T antigen inhibits expression of MyoD and myogenin, up-regulates Myf-5, but does not affect early expression of desmin or alpha 7 integrin during muscle development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Synapse Formation Between Two Clonal Cell Lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

High efficiency of muscle regeneration after human myoblast clone transplantation in SCID mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Transplantation of myoblasts from a transgenic mouse overexpressing dystrophin produced only a relatively small increase of dystrophin-positive membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Appearance of the Myofibroblastic Phenotype in Dupuytren&rsquo;s Disease Is Associated with a Fibronectin, Laminin, Collagen Type IV and Tenascin Extracellular Matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Laminins of the adult mammalian CNS; laminin-α2 (merosin M-) chain immunoreactivity is associated with neuronal processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Normal myogenic cells from newborn mice restore normal histology to degenerating muscles of the mdx mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Successful histocompatible myoblast transplantation in dystrophin-deficient mdx mouse despite the production of antibodies against dystrophin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Development of approaches to improve cell survival in myoblast transfer therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Successful transplantation of genetically corrected DMD myoblasts following ex vivo transduction with the dystrophin minigene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Anti-inflammatory effect of transforming growth factor-beta1 in myoblast transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Isolation of human myoblasts with the fluorescence-activated cell sorter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Formation of new muscle fibres and tumours after injection of cultured myogenic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Very efficient myoblast allotransplantation in mice under FK506 immunosuppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Pretreatment of myoblast cultures with basic fibroblast growth factor increases the efficacy of their transplantation in mdx mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Successive injections in MDX mice of myoblasts grown with bFGF

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

The inhibition of cultured myoblast differentiation by the simian virus 40 large T antigen occurs after myogenin expression and Rb up-regulation and is not exerted by transformation-competent cytoplasmic mutants.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

Internal initiation of translation in retroviral vectors carrying picornavirus 5' nontranslated regions.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

Prior culture with concanavalin A increases intramuscular migration of transplanted myoblast

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

A histochemical method for localizing cholinesterase activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3300889

7 January 2021

Identifiers

DOI

10.1038/SJ.GT.3300889

1 reference

Dimensions Publication ID

24 September 2017

1053453482

0 references

1 reference