Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells

Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) chloride (Cl-) channel regulated by protein kinases, phosphatases, divalent cations and by protein-protein interac...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Calvez, Marie-Laure, Benz, Nathalie, Huguet, Florentin, Saint-Pierre, Aude, Rouillé, Elise, Coraux, Christelle, Férec, Claude, Kerbiriou, Mathieu, Trouvé, Pascal
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5690610/
https://ncbi.nlm.nih.gov/pubmed/29145426
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0187774
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados