CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice

In cystic fibrosis (CF), a lack of functional CF transmembrane conductance regulator (CFTR) chloride channels causes defective secretion by submucosal glands (SMGs), leading to persistent bacterial infection that damages airways and necessitates tissue repair. SMGs are also important niches for slow...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Xie, Weiliang, Fisher, John T., Lynch, Thomas J., Luo, Meihui, Evans, Turan I.A., Neff, Traci L., Zhou, Weihong, Zhang, Yulong, Ou, Yi, Bunnett, Nigel W., Russo, Andrew F., Goodheart, Michael J., Parekh, Kalpaj R., Liu, Xiaoming, Engelhardt, John F.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2011
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3148720/
https://ncbi.nlm.nih.gov/pubmed/21765217
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI41857
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars