(Q81499314)

English

Characterization of a complex Duchenne muscular dystrophy-causing dystrophin gene inversion and restoration of the reading frame by induced exon skipping

scientific article published on 01 January 2009

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18570328%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Characterization of a complex Duchenne muscular dystrophy-causing dystrophin gene inversion and restoration of the reading frame by induced exon skipping (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18570328%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

2

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9 January 2020

author name string

Heidi R Madden

1

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Europe PubMed Central

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9 January 2020

Mark R Davis

3

1 reference

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9 January 2020

Steve D Wilton

4

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9 January 2020

publication date

1 January 2009

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9 January 2020

1 reference

Europe PubMed Central

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9 January 2020

30

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9 January 2020

1

1 reference

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9 January 2020

22-28

1 reference

Europe PubMed Central

PubMed publication ID

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9 January 2020

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

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Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistries

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Restoration of dystrophin expression in mdx muscle cells by chimeraplast-mediated exon skipping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Function and genetics of dystrophin and dystrophin-related proteins in muscle

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

ESEfinder: A web resource to identify exonic splicing enhancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular, cellular, and pharmacological therapies for Duchenne/Becker muscular dystrophies.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A G-->A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Becker muscular dystrophy with onset after 60 years.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystrophin, the protein product of the Duchenne/Becker muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

A point mutation in the human estrogen receptor gene is associated with the expression of an abnormal estrogen receptor mRNA containing a 69 novel nucleotide insertion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcript.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20806

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20806

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18570328%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18570328%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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