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Antiproteases as Therapeutics to Target Inflammation in Cystic Fibrosis

Cystic Fibrosis (CF) is the most common fatal inherited disease of Caucasians, affecting about 1 in 3000 births. Patients with CF have a recessive mutation in the gene encoding the CF transmembrane conductance regulator (CFTR). CFTR is expressed in the epithelium of many organs throughout the exocri...

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Autors principals: Quinn, Derek J, Weldon, Sinéad, Taggart, Clifford C
Format: Artigo
Idioma:Inglês
Publicat: Bentham Open 2010
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2864511/
https://ncbi.nlm.nih.gov/pubmed/20448835
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1874306401004010020
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