Postnatal airway growth in cystic fibrosis piglets

Mutations in the gene encoding the cystic fibrosis (CF) transmembrane conductance regulator (CFTR) anion channel cause CF. The leading cause of death in the CF population is lung disease. Increasing evidence suggests that in utero airway development is CFTR-dependent and that developmental abnormali...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Appl Physiol (1985)
Autors principals: Adam, Ryan J., Abou Alaiwa, Mahmoud H., Bouzek, Drake C., Cook, Daniel P., Gansemer, Nicholas D., Taft, Peter J., Powers, Linda S., Stroik, Mallory R., Hoegger, Mark J., McMenimen, James D., Hoffman, Eric A., Zabner, Joseph, Welsh, Michael J., Meyerholz, David K., Stoltz, David A.
Format: Artigo
Idioma:Inglês
Publicat: American Physiological Society 2017
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5625074/
https://ncbi.nlm.nih.gov/pubmed/28620056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/japplphysiol.00263.2017
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars