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Gene therapy for cystic fibrosis lung disease

Cystic fibrosis (CF) is characterised by respiratory and pancreatic deficiencies that stem from the loss of fully functional CFTR (CF transmembrane conductance regulator) at the membrane of epithelial cells. Current treatment modalities aim to delay the deterioration in lung function, Which is mostl...

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Publicat a:Gene Therapy for Autoimmune and Inflammatory Diseases
Autors principals: Sumner-Jones, Stephanie G., Gill, Deborah R., Hyde, Stephen C.
Format: Artigo
Idioma:Inglês
Publicat: 2011
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7115003/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-0346-0165-8_4
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