Restoration of W1282X CFTR Activity by Enhanced Expression

Cystic fibrosis results from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Premature termination codons represent a common minority of CFTR mutations, and are caused by base pair substitutions that produce abnormal stop codons in the coding sequence. Select aminog...

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Bibliografiska uppgifter
Huvudupphovsmän: Rowe, Steven M., Varga, Karoly, Rab, Andras, Bebok, Zsuzsa, Byram, Kevin, Li, Yao, Sorscher, Eric J., Clancy, John P.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Thoracic Society 2007
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Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1994229/
https://ncbi.nlm.nih.gov/pubmed/17541014
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1165/rcmb.2006-0176OC
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