(Q35855342)

English

No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations

scientific article published on 8 March 2007

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

10 August 2017

No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations (English)

1 reference

Europe PubMed Central

10 August 2017

cystic fibrosis

0 references

transmembrane protein

0 references

author name string

John P Clancy

1

1 reference

Europe PubMed Central

10 August 2017

Steven M Rowe

2

1 reference

Europe PubMed Central

10 August 2017

Zsuzsa Bebok

3

1 reference

Europe PubMed Central

10 August 2017

Moira L Aitken

4

1 reference

Europe PubMed Central

10 August 2017

Ron Gibson

5

1 reference

Europe PubMed Central

10 August 2017

Pam Zeitlin

6

1 reference

Europe PubMed Central

10 August 2017

Pierre Berclaz

7

1 reference

Europe PubMed Central

10 August 2017

Rick Moss

8

1 reference

Europe PubMed Central

10 August 2017

Michael R Knowles

9

1 reference

Europe PubMed Central

10 August 2017

Robert A Oster

10

1 reference

Europe PubMed Central

10 August 2017

Nicole Mayer-Hamblett

11

1 reference

Europe PubMed Central

10 August 2017

Bonnie Ramsey

12

1 reference

Europe PubMed Central

10 August 2017

publication date

8 March 2007

1 reference

Europe PubMed Central

10 August 2017

American Journal of Respiratory Cell and Molecular Biology

1 reference

Europe PubMed Central

10 August 2017

37

1 reference

Europe PubMed Central

10 August 2017

1

1 reference

Europe PubMed Central

10 August 2017

57-66

1 reference

Europe PubMed Central

10 August 2017

Standardized procedure for measurement of nasal potential difference: an outcome measure in multicenter cystic fibrosis clinical trials

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Genomics as a probe for disease biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Aminoglycoside and its derivatives as ligands to target the ribosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Killing the messenger: new insights into nonsense-mediated mRNA decay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of alpha-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

A BRCA1 nonsense mutation causes exon skipping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Genotype-phenotype correlations in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

11 July 2018

Clinically relevant aminoglycosides can suppress disease-associated premature stop mutations in the IDUA and P53 cDNAs in a mammalian translation system

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

Effects of pressure support ventilation plus volume guarantee vs. high-frequency oscillatory ventilation on lung inflammation in preterm infants.

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

Pulmonary sarcoidosis in a 14-year-old boy diagnosed by low-dose CT-guided transthoracic lung biopsy.

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

Dexamethasone alleviates meconium-induced airway hyperresponsiveness and lung inflammation in rabbits

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

Use of nasal potential difference and sweat chloride as outcome measures in multicenter clinical trials in subjects with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

A multicenter study of the effect of solution temperature on nasal potential difference measurements

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899350

24 September 2018

Interactions of a small RNA with antibiotic and RNA ligands of the 30S subunit

1 reference

https://api.crossref.org/works/10.1165%2FRCMB.2006-0173OC

21 January 2018

Correlation between genotype and phenotype in patients with cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17347447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17347447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype and phenotype in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17347447

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/17347447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CFTR nonsense mutations G542X and W1282X associated with severe reduction of CFTR mRNA in nasal epithelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17347447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1165/RCMB.2006-0173OC

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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