(Q58108925)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502 AND SRC:MED&resulttype=core&format=json

31 October 2019

title

Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502 AND SRC:MED&resulttype=core&format=json

genotype-phenotype correlation

31 October 2019

main subject

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1 reference

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6

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31 October 2019

author name string

L T Guo

1

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31 October 2019

X U Zhang

2

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31 October 2019

W Kuang

3

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31 October 2019

H Xu

4

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31 October 2019

L A Liu

5

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31 October 2019

Y Miyagoe-Suzuki

7

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31 October 2019

S Takeda

8

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31 October 2019

M A Ruegg

9

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31 October 2019

U M Wewer

10

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31 October 2019

E Engvall

11

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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)

207-215

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Congenital muscular dystrophies: 1997 update

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Congenital muscular dystrophy: an expanding clinical syndrome

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Molecular basis of muscular dystrophies.

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Congenital myopathies and congenital muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Dystrophin and muscular dystrophy: past, present, and future

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Merosin and congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

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/S0960-8966(02)00266-3

7 January 2021

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Animal models for muscular dystrophy: valuable tools for the development of therapies

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

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/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Cloning and expression of laminin alpha 2 chain (M-chain) in the mouse

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Localization of Heparin Binding Activity in Recombinant Laminin G Domain

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

P0 promoter directs expression of reporter and toxin genes to Schwann cells of transgenic mice

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Indicator expression directed by regulatory sequences of the glial fibrillary acidic protein (GFAP) gene: in vivo comparison of distinct GFAP-lacZ transgenes

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Distinct regions control transcriptional activation of the alpha1(VI) collagen promoter in different tissues of transgenic mice

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

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/S0960-8966(02)00266-3

7 January 2021

Distribution of ten laminin chains in dystrophic and regenerating muscles

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0960-8966(02)00266-3

7 January 2021

10.1016/S0960-8966(02)00266-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502 AND SRC:MED&resulttype=core&format=json

31 October 2019

1 reference