Exploring the frontiers of therapeutic exon skipping for Duchenne muscular dystrophy by double targeting within one or multiple exons (Q83925361)

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29 January 2020

title

Exploring the frontiers of therapeutic exon skipping for Duchenne muscular dystrophy by double targeting within one or multiple exons (English)

1 reference

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Duchenne muscular dystrophy

29 January 2020

main subject

1 reference

based on heuristic

inferred from title

author name string

Annemieke Aartsma-Rus

1

1 reference

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29 January 2020

Wendy E Kaman

2

1 reference

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29 January 2020

Rudie Weij

3

1 reference

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29 January 2020

Johan T den Dunnen

4

1 reference

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29 January 2020

Gert-Jan B van Ommen

5

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29 January 2020

Judith C T van Deutekom

6

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29 January 2020

publication date

6 June 2006

1 reference

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29 January 2020

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29 January 2020

volume

14

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issue

3

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29 January 2020

page(s)

401-407

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29 January 2020

cites work

The muscular dystrophies

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

7 January 2021

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Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

7 January 2021

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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

7 January 2021

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Glycoprotein complex anchoring dystrophin to sarcolemma

7 January 2021

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

7 January 2021

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

7 January 2021

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Advances in Duchenne muscular dystrophy gene therapy

7 January 2021

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Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients.

7 January 2021

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Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells

7 January 2021

1 reference

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Antisense-induced multiexon skipping for Duchenne muscular dystrophy makes more sense

7 January 2021

1 reference

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Targeted exon skipping in transgenic hDMD mice: A model for direct preclinical screening of human-specific antisense oligonucleotides

7 January 2021

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Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles

7 January 2021

1 reference

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

7 January 2021

1 reference

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Functional analysis of 114 exon-internal AONs for targeted DMD exon skipping: indication for steric hindrance of SR protein binding sites

7 January 2021

1 reference

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SR protein kinases: the splice of life

7 January 2021

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LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

7 January 2021

1 reference

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

7 January 2021

1 reference

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Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy.

7 January 2021

1 reference

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Deletion status and intellectual impairment in Duchenne muscular dystrophy.

7 January 2021

1 reference

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The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced

7 January 2021

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Exploiting the natural diversity in adenovirus tropism for therapy and prevention of disease

7 January 2021

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10.1016/J.YMTHE.2006.02.022

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16753346%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference