Epithelial IgG and its relationship to the loss of F508 in the common mutant form of the cystic fibrosis transmembrane conductance regulator

The most debilitating feature of cystic fibrosis (CF) disease is uncontrolled inflammation of respiratory epithelium. The relationship between the commonest mutated form of CFTR (F508del or ΔF508) and inflammation has not yet been elucidated. Here, we present a new paradigm suggesting that CFTR can...

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Detalles Bibliográficos
Autores principales: Treharne, Kate J., Cassidy, Diane, Goddard, Catharine, Colledge, William H., Cassidy, Andrew, Mehta, Anil
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741568/
https://www.ncbi.nlm.nih.gov/pubmed/19596328
http://dx.doi.org/10.1016/j.febslet.2009.07.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741568/
https://www.ncbi.nlm.nih.gov/pubmed/19596328
http://dx.doi.org/10.1016/j.febslet.2009.07.002

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