Reversal of cystic fibrosis phenotype in a cultured Δ508 cystic fibrosis transmembrane conductance regulator cell line by oligonucleotide insertion

Cystic fibrosis (CF) is a lethal genetic disorder that is due to mutations in the gene encoding the cAMP-activated anion CF transmembrane conductance regulator (CFTR) channel. A three-nucleotide base deletion (TTT), encoding phenylalanine in position 508 of the translatable CFTR sequence (accompanie...

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Detaylı Bibliyografya

Yayımlandı:	Proc Natl Acad Sci U S A
Asıl Yazarlar:	Zamecnik, Paul C., Raychowdhury, Malay K., Tabatadze, David R., Cantiello, Horacio F.
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	National Academy of Sciences 2004
Konular:	Biological Sciences
Online Erişim:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC419572/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15148387/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0401933101
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