(Q42831325)

English

Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment.

scientific article published on April 2004

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scholarly article

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23 November 2019

Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14973546%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

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23 November 2019

Jean-Jacques Panthier

5

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23 November 2019

author name string

Bidou L

1

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23 November 2019

Perez N

3

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23 November 2019

Allamand V

4

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23 November 2019

Rousset JP

6

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23 November 2019

publication date

1 April 2004

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23 November 2019

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23 November 2019

11

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23 November 2019

7

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23 November 2019

619-627

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23 November 2019

Aminoglycoside suppression at UAG, UAA and UGA codons in Escherichia coli and human tissue culture cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Structure of the 30S ribosomal subunit

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Suppression of a nonsense mutation in mammalian cells in vivo by the aminoglycoside antibiotics G-418 and paromomycin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Aminoglycoside suppression of a premature stop mutation in a Cftr-/- mouse carrying a human CFTR-G542X transgene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscle

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

The efficiency of translation termination is determined by a synergistic interplay between upstream and downstream sequences in Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Impact of the six nucleotides downstream of the stop codon on translation termination

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Aminoglycoside antibiotics mediate context-dependent suppression of termination codons in a mammalian translation system

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Versatile vectors to study recoding: conservation of rules between yeast and mammalian cells.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Aminoglycoside toxicity - a review of clinical studies published between 1975 and 1982

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Tetracycline transcriptional silencer tightly controls transgene expression after in vivo intramuscular electrotransfer: application to interleukin 10 therapy in experimental arthritis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

The signal for a leaky UAG stop codon in several plant viruses includes the two downstream codons

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

UAG readthrough is not increased in vivo by Moloney murine leukemia virus infection

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

UAG readthrough in mammalian cells: effect of upstream and downstream stop codon contexts reveal different signals

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Phenotypic suppression of nonsense mutants in yeast by aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Phenotypic suppression and misreading in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Modulation of RNA function by aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Release factor RF-3 GTPase activity acts in disassembly of the ribosome termination complex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

High-efficiency gene transfer into skeletal muscle mediated by electric pulses

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

21 January 2018

Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Hidden infidelities of the translational stop signal

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Misrouting of tyrosinase with a truncated cytoplasmic tail as a result of the murine platinum (cp) mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of the nucleotide 3' to an amber codon on ribosomal selection rates of suppressor tRNA and release factor-1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Translational readthrough of the PDE2 stop codon modulates cAMP levels in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302211

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.GT.3302211

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14973546%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14973546%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

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