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Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
title
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
author
Kylie S Carville
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
Sue Fletcher
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
Ryszard Kole
series ordinal
7
object named as
R Kole
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
author name string
S D Wilton
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
F Lloyd
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
K Honeyman
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
S Agrawal
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
publication date
1 July 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
page(s)
330-338
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
cites work
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
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7 January 2021
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X chromosome-linked muscular dystrophy (mdx) in the mouse
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7 January 2021
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7 January 2021
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7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic reversion/suppression of the mouse mdx phenotype in vivo.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy
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reference URL
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7 January 2021
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Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course
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7 January 2021
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Immunohistological evidence for second or somatic mutations as the underlying cause of dystrophin expression by isolated fibres in Xp21 muscular dystrophy of Duchenne-type severity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
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Dystrophin gene transcripts skipping the mdx mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Antisense oligonucleotides as antiviral agents
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of promoter-specific repression by triple-helical DNA complexes in a eukaryotic cell-free transcription system
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antisense and Antigene Properties of Peptide Nucleic Acids
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Repair of thalassemic human beta-globin mRNA in mammalian cells by antisense oligonucleotides
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https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Exon structure of the human dystrophin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
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inferred from DOI database lookup
RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
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7 January 2021
based on heuristic
inferred from DOI database lookup
Stability of the human dystrophin transcript in muscle
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystrophin is transcribed in brain from a distant upstream promoter.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel dystrophin isoform is required for normal retinal electrophysiology.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Dp140: a novel 140 kDa CNS transcript from the dystrophin locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
An alternative dystrophin transcript specific to peripheral nerve
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
PCR and immunocytochemical analyses of dystrophin-positive fibers in Duchenne muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Order of intron removal during splicing of endogenous adenine phosphoribosyltransferase and dihydrofolate reductase pre-mRNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct gene transfer into muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RNase H cleavage of RNA hybridized to oligonucleotides containing methylphosphonate, phosphorothioate and phosphodiester bonds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stable alteration of pre-mRNA splicing patterns by modified U7 small nuclear RNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900010-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(99)00010-3
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
PubMed ID
10407856
1 reference
stated in
Europe PubMed Central
PubMed ID
10407856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
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