Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy. (Q34580135)

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31 December 2019

review article

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title

Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17555369%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

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31 December 2019

Kanneboyina Nagaraju

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31 December 2019

Toshifumi Yokota

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31 December 2019

Emidio Pistilli

series ordinal

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31 December 2019

language of work or name

English

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publication date

1 June 2007

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Expert Opinion on Biological Therapy

31 December 2019

published in

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31 December 2019

volume

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31 December 2019

issue

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31 December 2019

page(s)

831-842

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

31 December 2019

cites work

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

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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

21 January 2018

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Expression of the murine Duchenne muscular dystrophy gene in muscle and brain

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Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain

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SH3 domain-mediated interaction of dystroglycan and Grb2

21 January 2018

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Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

21 January 2018

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21 January 2018

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

21 January 2018

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Becker muscular dystrophy with onset after 60 years.

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Suppression of revertant fibers in mdx mice by expression of a functional dystrophin.

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Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients

21 January 2018

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Somatic reversion/suppression of the mouse mdx phenotype in vivo.

21 January 2018

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

21 January 2018

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Maintenance of an open reading frame as an additional level of scrutiny during splice site selection

21 January 2018

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Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions

21 January 2018

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Dystrophin expression in the mdx mouse after localised and systemic administration of a morpholino antisense oligonucleotide

21 January 2018

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Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology

21 January 2018

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Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence

21 January 2018

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

21 January 2018

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Therapeutic restoration of dystrophin expression in Duchenne muscular dystrophy.

21 January 2018

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

21 January 2018

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Boranophosphates as mimics of natural phosphodiesters in DNA.

21 January 2018

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Rationally targeted, conformationally constrained, oxetane-modified oligonucleotides demonstrate efficient gene-silencing activity in a cellular system

21 January 2018

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Promising nucleic acid analogs and mimics: characteristic features and applications of PNA, LNA, and morpholino

21 January 2018

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Building oligonucleotide therapeutics using non-natural chemistries

21 January 2018

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

21 January 2018

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells

21 January 2018

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Morpholino antisense oligomers: design, preparation, and properties

21 January 2018

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Resistance of morpholino phosphorodiamidate oligomers to enzymatic degradation

21 January 2018

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Listening to silence and understanding nonsense: exonic mutations that affect splicing

21 January 2018

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Tissue-engineered human bioartificial muscles expressing a foreign recombinant protein for gene therapy

21 January 2018

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128th ENMC International Workshop on 'Preclinical optimization and Phase I/II Clinical Trials Using Antisense Oligonucleotides in Duchenne Muscular Dystrophy' 22-24 October 2004, Naarden, The Netherlands

21 January 2018

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Induction of revertant fibres in the mdx mouse using antisense oligonucleotides

21 January 2018

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Targeted Disruption of Exon 52 in the Mouse Dystrophin Gene Induced Muscle Degeneration Similar to That Observed in Duchenne Muscular Dystrophy

21 January 2018

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Differential expression of dystrophin isoforms in strains of mdx mice with different mutations

21 January 2018

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Cardiac involvement in Beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies

21 January 2018

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Gene transfer with microbubble ultrasound and plasmid DNA into skeletal muscle of mice: comparison between commercially available microbubble contrast agents

21 January 2018

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21 January 2018

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Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping

21 January 2018

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21 January 2018

Identifiers

DOI

10.1517/14712598.7.6.831

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17555369%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

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