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...

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Библиографические подробности
Опубликовано в: :PLoS One
Главные авторы: Calvez, Marie-Laure, Benz, Nathalie, Huguet, Florentin, Saint-Pierre, Aude, Rouillé, Elise, Coraux, Christelle, Férec, Claude, Kerbiriou, Mathieu, Trouvé, Pascal
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2017
Предметы:
Research Article
Online-ссылка: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
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