The cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in maturation stage ameloblasts, odontoblasts and bone cells

Author:

Bronckers Antonius,Kalogeraki Lida,Jorna Huub J.N.,Wilke Martina,Bervoets Theodore J.,Lyaruu Donacian M.,Zandieh-Doulabi Behrouz,DenBesten Pamela,de Jonge Hugo

Funder

NIH

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference59 articles.

1. Cystic fibrosis: a molecular biology and therapeutic implications;Collins;Science,1992

2. Dynamic control of cystic fibrosis transmembrane conductance regulator Cl-/ HCO3- selectivity by external Cl-;Shcheynikov;J. Biol. Chem.,2004

3. Cystic fibrosis transmembrane conductance regulator and Slc26 transporters in HCO3 secretion by pancreatic duct cells;Ishiguro;Acta Physiol. Sinica,2007

4. CFTR functions as a bicarbonate channel in pancreatic duct cells;Ishiguro;J. Gen. Physiol.,2009

5. Mechanisms of bicarbonate secretion in the pancreatic duct;Steward;Ann. Rev. Physiol.,2005

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