Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene (Q44020748)

29 November 2017

Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene (English)

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29 November 2017

Miki Sakamoto

1

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29 November 2017

Katsutoshi Yuasa

2

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29 November 2017

Madoka Yoshimura

3

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29 November 2017

Toshifumi Yokota

4

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29 November 2017

Takaaki Ikemoto

5

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29 November 2017

Misao Suzuki

6

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29 November 2017

George Dickson

7

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29 November 2017

Yuko Miyagoe-Suzuki

8

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29 November 2017

Shin'ichi Takeda

9

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29 November 2017

language of work or name

English

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publication date

1 May 2002

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Biochemical and Biophysical Research Communications

29 November 2017

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29 November 2017

293

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29 November 2017

4

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29 November 2017

1265-1272

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

29 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Analysis of the actin-binding domain of alpha-actinin by mutagenesis and demonstration that dystrophin contains a functionally homologous domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Role of nitric oxide in the pathogenesis of muscular dystrophies: a "two hit" hypothesis of the cause of muscle necrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Gene therapy for muscular dystrophies: current status and future prospects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Effective restoration of dystrophin-associated proteins in vivo by adenovirus-mediated transfer of truncated dystrophin cDNAs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Effective adenovirus-mediated gene expression in adult murine skeletal muscle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Efficient selection for high-expression transfectants with a novel eukaryotic vector

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Immune response to adenovirus-delivered antigens upregulates utrophin and results in mitigation of muscle pathology in mdx mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Contractile properties of diaphragm muscle segments from old mdx and old transgenic mdx mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Site-specific recombination of a transgene in fertilized eggs by transient expression of Cre recombinase.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

A cluster of basic repeats in the dystrophin rod domain binds F-actin through an electrostatic interaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900362-5

10.1016/S0006-291X(02)00362-5

7 January 2021

Identifiers

DOI

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29 November 2017

1 reference