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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:J Appl Physiol (1985)
Main Authors: 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
Sprog:Inglês
Udgivet: American Physiological Society 2017
Fag:
Research Article
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker