(Q73918582)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

congenital muscular dystrophy

7 November 2019

main subject

1 reference

6

E P Hoffman

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

Y K Hayashi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Z Tezak

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

T Momoi

3

1 reference

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7 November 2019

I Nonaka

4

1 reference

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7 November 2019

C A Garcia

5

1 reference

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7 November 2019

K Arahata

7

1 reference

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7 November 2019

publication date

1 May 2001

1 reference

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7 November 2019

published in

Neuromuscular Disorders

1 reference

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7 November 2019

volume

11

1 reference

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7 November 2019

issue

4

1 reference

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7 November 2019

page(s)

350-359

1 reference

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

7 November 2019

cites work

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands

1 reference

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7 January 2021

Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

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%2800%2900203-0

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%2800%2900203-0

7 January 2021

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Distribution of ten laminin chains in dystrophic and regenerating muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Abnormal localization of laminin subunits in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Mutations in the integrin alpha7 gene cause congenital myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Detection of activated caspase-3 (CPP32) in the vertebrate nervous system during development by a cleavage site-directed antiserum.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Akt phosphorylation site found in human caspase-9 is absent in mouse caspase-9.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

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%2800%2900203-0

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%2800%2900203-0

7 January 2021

Complement activation in muscle fiber necrosis: demonstration of the membrane attack complex of complement in necrotic fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Membrane defence against complement lysis: the structure and biological properties of CD59.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Expression of CD59, a regulator of the membrane attack complex of complement, on human skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

A role for mast cells in the progression of Duchenne muscular dystrophy? Correlations in dystrophin-deficient humans, dogs, and mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Myocardial infarction and apoptosis after myocardial ischemia and reperfusion: role of the terminal complement components and inhibition by anti-C5 therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

C5b-9 membrane attack complex mediates endothelial cell apoptosis in experimental glomerulonephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Diminished expression of CD59 on activated CD8+ T cells undergoing apoptosis in systemic lupus erythematosus and Sjögren's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Terminal complement complexes concomitantly stimulate proliferation and rescue of Schwann cells from apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900203-0

7 January 2021

10.1016/S0960-8966(00)00203-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11369186%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference