In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study (Q33280494)

25 July 2017

In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study (English)

1 reference

Correction to: In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study

25 July 2017

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corrigendum / erratum

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Laure Bidou

4

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Aleksander Edelman

13

object named as

Aleksander Edelman

1 reference

25 July 2017

Isabelle Sermet-Gaudelus

1

object named as

Isabelle Sermet-Gaudelus

1 reference

25 July 2017

10

Gérard Lenoir

1 reference

25 July 2017

3

Anne Fajac

1 reference

25 July 2017

Michel Renouil

2

1 reference

25 July 2017

Bastien Parbaille

5

1 reference

25 July 2017

Sébastien Pierrot

6

1 reference

25 July 2017

Nolwen Davy

7

1 reference

25 July 2017

Elise Bismuth

8

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25 July 2017

Philippe Reinert

9

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25 July 2017

Jean François Lesure

11

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25 July 2017

Jean Pierre Rousset

12

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25 July 2017

language of work or name

English

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publication date

29 March 2007

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25 July 2017

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25 July 2017

5

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25 July 2017

5

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https://scigraph.springernature.com/pub.10.1186/1741-7015-5-5

25 July 2017

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cites work

Pharmacologic therapy for stop mutations: how much CFTR activity is enough?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Antibodies for CFTR studies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Extended-interval aminoglycoside administration for children: a meta-analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis andCFTRStop Mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Functional insights from the structure of the 30S ribosomal subunit and its interactions with antibiotics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Hidden infidelities of the translational stop signal

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1741-7015-5-5

Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852113

Cystic fibrosis clinical score: a new scoring system to evaluate acute pulmonary exacerbation

31 October 2018

1 reference

12 December 2020

Clinical doses of amikacin provide more effective suppression of the human CFTR-G542X stop mutation than gentamicin in a transgenic CF mouse model

1 reference

12 December 2020

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

1 reference

12 December 2020

A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island

1 reference

12 December 2020

Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

1 reference

12 December 2020

Identifiers

DOI

10.1186/1741-7015-5-5

1 reference

Dimensions Publication ID

25 July 2017

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1 reference

25 July 2017

1 reference