Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. (Q41418979)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894482%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy (English)

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28 October 2019

3

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28 October 2019

author name string

Cox GA

series ordinal

1

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28 October 2019

Sunada Y

series ordinal

2

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28 October 2019

Chamberlain JS

series ordinal

4

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28 October 2019

language of work or name

English

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publication date

1 December 1994

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28 October 2019

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28 October 2019

volume

8

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28 October 2019

issue

4

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28 October 2019

page(s)

333-339

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

28 October 2019

cites work

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Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

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The structural and functional diversity of dystrophin

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An alternative dystrophin transcript specific to peripheral nerve

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A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

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Expression of the N-terminal domain of dystrophin in E. coli and demonstration of binding to F-actin.

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Interaction of dystrophin with cytoskeletal proteins: binding to talin and actin

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Deletion analysis of the dystrophin-actin binding domain

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Membrane organization of the dystrophin-glycoprotein complex

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A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

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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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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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Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

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Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy.

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A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

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Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy

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Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophy

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Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin

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

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7 January 2021

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

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7 January 2021

Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma

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7 January 2021

Characterization and cell type distribution of a novel, major transcript of the Duchenne muscular dystrophy gene

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7 January 2021

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

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7 January 2021

Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblasts

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7 January 2021

Muscle creatine kinase sequence elements regulating skeletal and cardiac muscle expression in transgenic mice

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7 January 2021

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin

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7 January 2021

Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus

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7 January 2021

Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development

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7 January 2021

Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasm

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7 January 2021

Dystrophin is phosphorylated by endogenous protein kinases

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7 January 2021

Calmodulin-activated phosphorylation of dystrophin

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7 January 2021

Primary structure of dystrophin-related protein

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7 January 2021

Expression of a dystrophin-related protein associated with the skeletal muscle cell membrane

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7 January 2021

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7 January 2021

Immunohistochemical dystrophin reaction in synaptic regions

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7 January 2021

Structure and function of the neuromuscular junction in young adultmdx mice

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7 January 2021

Animal models of muscular dystrophy – what can they teach us?

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7 January 2021

The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin

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7 January 2021

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

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7 January 2021

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

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7 January 2021

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

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7 January 2021

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

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7 January 2021

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

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7 January 2021

Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle

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7 January 2021

Expression of recombinant dystrophin and its localization to the cell membrane

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7 January 2021

Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma

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7 January 2021

Phosphorylation of phospholipase C in vivo and in vitro

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Identifiers

DOI

10.1038/NG1294-333

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894482%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

28 October 2019

1040752769

0 references

1 reference