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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Detalles Bibliográficos
Autores principales: Quinn, Derek J, Weldon, Sinéad, Taggart, Clifford C
Formato: Texto
Lenguaje:English
Publicado: Bentham Open 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864511/
https://www.ncbi.nlm.nih.gov/pubmed/20448835
http://dx.doi.org/10.2174/1874306401004010020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864511/
https://www.ncbi.nlm.nih.gov/pubmed/20448835
http://dx.doi.org/10.2174/1874306401004010020

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