(Q57270383)

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Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice

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12 November 2019

Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin alpha2-deficient mice (English)

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12 November 2019

muscular dystrophy

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1

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12 November 2019

author name string

R M Keeling

2

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12 November 2019

S Mehta

3

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12 November 2019

A Pestronk

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12 November 2019

J R Sanes

5

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12 November 2019

publication date

1 November 2001

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12 November 2019

Neuromuscular Disorders

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12 November 2019

11

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12 November 2019

8

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12 November 2019

703-712

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12 November 2019

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

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7 January 2021

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Muscular dystrophy in the mdx mouse: histopathology of the soleus and extensor digitorum longus muscles.

1 reference

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7 January 2021

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The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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Comparison of dy and dy2J, Two Alleles Expressing Forms of Muscular Dystrophy in the Mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Pre-clinical screening of drugs using the mdx mouse

1 reference

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7 January 2021

based on heuristic

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Fiber regeneration is not persistent in dystrophic (MDX) mouse skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystrophy and myogenesis in mdx diaphragm muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

1 reference

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7 January 2021

based on heuristic

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Forced expression of dystrophin deletion constructs reveals structure-function correlations.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Phenotype of dystrophinopathy in old mdx mice

1 reference

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7 January 2021

based on heuristic

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A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Subtle neuromuscular defects in utrophin-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

An ultrastructural study of degeneration and necrosis of muscle in the dystrophic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormalities of peripheral nerves in murine muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetically determined defect of Schwann cell basement membrane in dystrophic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Quantitative measurement of muscle strength in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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A simple recording grip strength device

1 reference

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7 January 2021

based on heuristic

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Motor dysfunction in a mouse model for Down syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Behavioral performance of Swiss Webster mice exposed to excess dietary aluminum during development or during development and as adults.

1 reference

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7 January 2021

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Long-term neuroprotective effects of glycosaminoglycans-IGF-I cotreatment in the motor neuron degeneration (mnd ) mutant mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Beneficial effects of insulin-like growth factor-I on wobbler mouse motoneuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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Neuronal nitric oxide synthase inhibitor, 7-nitroindazole, delays motor dysfunction and spinal motoneuron degeneration in the wobbler mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

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How does dystrophin deficiency lead to muscle degeneration?--evidence from the mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Morphological and functional study of extensor digitorum longus muscle regeneration after iterative crush lesions in mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Apoptosis, DNA damage and ubiquitin expression in normal and mdx muscle fibers after exercise

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical investigation in duchenne dystrophy: 2. Determination of the ?power? of therapeutic trials based on the natural history

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical investigation of Duchenne muscular dystrophy. Interesting results in a trial of prednisone

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical trial in Duchenne dystrophy. I. The design of the protocol

1 reference

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7 January 2021

based on heuristic

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Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Merosin/laminin-2 and muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of immunocytochemistry in congenital myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Distribution of ten laminin chains in dystrophic and regenerating muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Merosin and laminin. Molecular relationship and role in nerve-muscle development

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

A comparative freeze-fracture study of plasma membrane of dystrophic skeletal muscles in dy/dy mice with merosin (laminin 2) deficiency and mdx mice with dystrophin deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure and function of the neuromuscular junction in young adultmdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuromuscular transmission in the mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuromuscular transmission in dystrophic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900232-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(01)00232-2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11595512%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11595512%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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