Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice (Q40667755)

22 September 2017

title

Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice (English)

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22 September 2017

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Toshikuni Sasaoka

1

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22 September 2017

Michihiro Imamura

2

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22 September 2017

Kenji Araishi

3

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22 September 2017

Satoru Noguchi

4

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22 September 2017

Yuji Mizuno

5

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22 September 2017

Naomi Takagoshi

6

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22 September 2017

Hiroshi Hama

7

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22 September 2017

Eriko Wakabayashi-Takai

8

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22 September 2017

Yukiko Yoshimoto-Matsuda

9

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22 September 2017

Ikuya Nonaka

10

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22 September 2017

Kiyotoshi Kaneko

11

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22 September 2017

Mikiharu Yoshida

12

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22 September 2017

Eijiro Ozawa

13

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22 September 2017

language of work or name

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1 March 2003

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22 September 2017

published in

Neuromuscular Disorders

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22 September 2017

volume

13

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22 September 2017

issue

3

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22 September 2017

page(s)

193-206

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Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

22 September 2017

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Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

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Membrane organization of the dystrophin-glycoprotein complex

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Dystrophin-associated proteins in muscular dystrophy

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Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

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Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

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From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy

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

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Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart

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Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice

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Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle

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Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

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Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

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β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

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Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

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7 January 2021

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

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7 January 2021

Analysis of the spatial, temporal and tissue-specific transcription of gamma-sarcoglycan gene using a transgenic mouse

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7 January 2021

Identification of myogenesis-dependent transcriptional enhancers in promoter region of mouse gamma-sarcoglycan gene

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7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

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7 January 2021

Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles

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7 January 2021

Distribution of dystrophin isoforms and dystrophin-associated proteins 43DAG (A3a) and 50DAG (A2) in various monkey tissues

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7 January 2021

Caveolin-3 deficiency causes muscle degeneration in mice

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7 January 2021

A sarcoglycan-dystroglycan complex anchors Dp116 and utrophin in the peripheral nervous system

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7 January 2021

Formation of sarcoglycan complex with differentiation in cultured myocytes

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7 January 2021

Developmental expression of sarcoglycan gene products in cultured myocytes

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7 January 2021

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

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7 January 2021

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies

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7 January 2021

mdx mice show progressive weakness and muscle deterioration with age

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7 January 2021

Phenotype of dystrophinopathy in old MDX mice

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7 January 2021

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.

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7 January 2021

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

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7 January 2021

Canine X-linked muscular dystrophy: Selective involvement of muscles in neonatal dogs

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7 January 2021

Functional regeneration in the hindlimb skeletal muscle of the mdx mouse

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7 January 2021

Muscle degeneration without mechanical injury in sarcoglycan deficiency

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7 January 2021

Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse

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7 January 2021

The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation

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7 January 2021

The mdx mouse skeletal muscle myopathy: II. Contractile properties

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7 January 2021

Further aspects of muscular dystrophy in mdx mice

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7 January 2021

Muscular dystrophy in a litter of golden retriever dogs

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7 January 2021

Canine X-linked muscular dystrophy: morphologic lesions

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7 January 2021

Dystrophin deficiency causes lethal muscle hypertrophy in cats

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7 January 2021

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

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7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900220-1

7 January 2021

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900220-1

7 January 2021

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

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https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900220-1

7 January 2021

Heart involvement in muscular dystrophies due to sarcoglycan gene mutations

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https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900220-1

7 January 2021

Cardiomyopathy in duchenne, becker, and sarcoglycanopathies: a role for coronary dysfunction?

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https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900220-1

7 January 2021

Evaluation of cardiac and respiratory involvement in sarcoglycanopathies

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7 January 2021

10.1016/S0960-8966(02)00220-1

Identifiers

DOI

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22 September 2017

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