Aminoglycosides

CF transmembrane conductance regulator ; Homo sapiens







10 Article(s)
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Pub. Year
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1 34272367 A small molecule that induces translational readthrough of CFTR nonsense mutations by eRF1 depletion. 2021 Jul 16 1
2 32640650 Investigating REPAIRv2 as a Tool to Edit CFTR mRNA with Premature Stop Codons. 2020 Jul 6 1
3 24251786 Synthetic aminoglycosides efficiently suppress cystic fibrosis transmembrane conductance regulator nonsense mutations and are enhanced by ivacaftor. 2014 Apr 2
4 21779978 Suppression of CFTR premature termination codons and rescue of CFTR protein and function by the synthetic aminoglycoside NB54. 2011 Nov 2
5 20829696 Cystic fibrosis transmembrane conductance regulator protein repair as a therapeutic strategy in cystic fibrosis. 2010 Nov 1
6 15510065 Pharmacologic therapy for stop mutations: how much CFTR activity is enough? 2004 Nov 1
7 12226741 Aminoglycoside suppression of a premature stop mutation in a Cftr-/- mouse carrying a human CFTR-G542X transgene. 2002 Sep 1
8 10712334 A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations. 2000 Mar 1
9 9359706 Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line. 1997 Nov 1
10 8597960 Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations. 1996 Apr 4