(Q58108941)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609503%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene (English)

1 reference

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31 October 2019

1 reference

3

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31 October 2019

Zhenlin Li

4

1 reference

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31 October 2019

Nicolas Vignier

6

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31 October 2019

Pascale Guicheney

9

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31 October 2019

author name string

Sylvie Besse

1

1 reference

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31 October 2019

Valérie Allamand

2

1 reference

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31 October 2019

Christophe Poirier

5

1 reference

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31 October 2019

Hisae Hori

7

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31 October 2019

Jean-Louis Guénet

8

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31 October 2019

publication date

1 March 2003

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31 October 2019

published in

Neuromuscular Disorders

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31 October 2019

volume

13

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31 October 2019

issue

3

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31 October 2019

page(s)

216-222

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

31 October 2019

cites work

1 reference

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7 January 2021

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

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7 January 2021

A new nomenclature for the laminins

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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

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

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7 January 2021

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

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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

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

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7 January 2021

Human laminin M chain: epitope analysis of its monoclonal antibodies by immunoscreening of cDNA clones and tissue expression

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7 January 2021

A general method for isolation of high molecular weight DNA from eukaryotes

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7 January 2021

A comprehensive genetic map of the mouse genome.

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7 January 2021

A Macintosh program for storage and analysis of experimental genetic mapping data

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7 January 2021

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

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7 January 2021

Myopathies caused by three mutations of the mouse

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7 January 2021

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.

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7 January 2021

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy

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7 January 2021

Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy.

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7 January 2021

Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion.

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7 January 2021

The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element

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7 January 2021

Intracisternal A-particle genes as movable elements in the mouse genome

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7 January 2021

Terminally redundant sequences in cellular intracisternal A-particle genes

1 reference

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7 January 2021

Sequences associated with intracisternal a particles are reiterated in the mouse genome

1 reference

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7 January 2021

Intracisternal A-particle genes: identification in the genome of Mus musculus and comparison of multiple isolates from a mouse gene library

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7 January 2021

Sequence organization of cloned intracisternal a particle genes

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7 January 2021

Mutant immunoglobulin genes have repetitive DNA elements inserted into their intervening sequences.

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7 January 2021

Inherited somatic mosaicism caused by an intracisternal A particle insertion in the mouse tyrosinase gene

1 reference

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7 January 2021

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

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7 January 2021

The laminin alpha2 expressed by dystrophic dy(2J) mice is defective in its ability to form polymers

1 reference

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7 January 2021

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Identifiers

DOI

1 reference

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31 October 2019

1 reference