(Q24339386)

GOA release 2020-03-11

1 reference

5

Volker Straub

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author name string

Richard Charlton

1

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Matthew Henderson

2

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Julie Richards

3

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Judith Hudson

4

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Kate Bushby

6

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Rita Barresi

Calpain translocation during muscle fiber necrosis and regeneration in dystrophin-deficient mice

7

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language of work or name

English

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publication date

July 2009

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published in

Neuromuscular Disorders

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volume

19

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issue

7

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page(s)

449-57

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human development

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Multiplex Western blotting system for the analysis of muscular dystrophy proteins

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

How to tackle the diagnosis of limb-girdle muscular dystrophy 2A

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Localization of Calpain 3 in Human Skeletal Muscle and Its Alteration in Limb-Girdle Muscular Dystrophy 2A Muscle

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Limb-girdle muscular dystrophies--from genetics to molecular pathology

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Calpain 3 mRNA expression in mice after denervation and during muscle regeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

1 reference

7 January 2021

Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021

Protein defects in neuromuscular diseases

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2009.05.005

7 January 2021