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Genetic therapies for cystic fibrosis lung disease

The aim of gene therapy for cystic fibrosis (CF) lung disease is to efficiently and safely express the CF transmembrane conductance regulator (CFTR) in the appropriate pulmonary cell types. Although CF patients experience multi-organ disease, the chronic bacterial lung infections and associated infl...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Sinn, Patrick L., Anthony, Reshma M., McCray, Paul B.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2011
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3095059/
https://ncbi.nlm.nih.gov/pubmed/21422098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr104
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