10 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
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 |