THE CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) IS EXPRESSED IN MATURATION STAGE AMELOBLASTS, ODONTOBLASTS AND BONE CELLS

Patients with cystic fibrosis (CF) have mild defects in dental enamel. The gene mutated in these patients is CFTR, a Cl(−) channel involved in transepithelial salt- and water transport and bicarbonate secretion. We tested the hypothesis that Cftr channels are present and operating in the plasma memb...

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Autors principals: Bronckers, Antonius, Kalogeraki, Lida, Jorna, Huub J.N., Wilke, Martina, Bervoets, Theodore J., Lyaruu, Donacian M., Zandieh-Doulabi, Behrouz, DenBesten, Pamela, de Jonge, Hugo
Format: Artigo
Idioma:Inglês
Publicat: 2009
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2842452/
https://ncbi.nlm.nih.gov/pubmed/20004757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2009.12.002
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