(Q45863474)

17 December 2017

title

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse (English)

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17 December 2017

author name string

Qi Long Lu

1

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17 December 2017

Christopher J Mann

2

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17 December 2017

Fang Lou

3

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17 December 2017

George Bou-Gharios

4

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17 December 2017

Glenn E Morris

5

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17 December 2017

Shao-an Xue

6

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17 December 2017

Sue Fletcher

7

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17 December 2017

Terence A Partridge

8

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17 December 2017

Stephen D Wilton

9

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17 December 2017

language of work or name

English

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publication date

6 July 2003

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17 December 2017

published in

Nature Medicine

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17 December 2017

volume

9

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17 December 2017

page(s)

1009-1014

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17 December 2017

issue

8

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/nm897

exact match

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cites work

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

7 January 2021

Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell-like properties as the myogenic source

1 reference

7 January 2021

Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA

1 reference

7 January 2021

Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product

1 reference

7 January 2021

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

1 reference

7 January 2021

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1 reference

7 January 2021

Screening for antisense modulation of dystrophin pre-mRNA splicing

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7 January 2021

Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy.

1 reference

7 January 2021

Non-viral gene delivery in skeletal muscle: a protein factory

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7 January 2021

Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion

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7 January 2021

Adeno-associated virus vector-mediated minidystrophin gene therapy improves dystrophic muscle contractile function in mdx mice

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7 January 2021

Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides

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7 January 2021

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

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7 January 2021

Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?

1 reference

7 January 2021

Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides

1 reference

7 January 2021

Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells

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7 January 2021

Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy

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7 January 2021

Systemically delivered antisense oligomers upregulate gene expression in mouse tissues

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7 January 2021

A new blocking method for application of murine monoclonal antibody to mouse tissue sections.

1 reference

7 January 2021

Microbubble ultrasound improves the efficiency of gene transduction in skeletal muscle in vivo with reduced tissue damage

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7 January 2021

Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old

1 reference

7 January 2021

Identifiers

DOI

10.1038/NM897

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17 December 2017

Dimensions Publication ID

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17 December 2017