Papers associated with distal (and cftr)

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	Oxalate secretion is stimulated by a cAMP-dependent pathway in the mouse cecum., Whittamore JM., Pflugers Arch. February 1, 2023; 475 (2): 249-266.
	Protein kinase A regulates C-terminally truncated CaV 1.2 in Xenopus oocytes: roles of N- and C-termini of the α1C subunit., Oz S., J Physiol. May 15, 2017; 595 (10): 3181-3202.
	Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis., Faure G., J Mol Biol. July 17, 2016; 428 (14): 2898-915.
	CFTR is required for PKA-regulated ATP sensitivity of Kir1.1 potassium channels in mouse kidney., Lu M., J Clin Invest. March 1, 2006; 116 (3): 797-807.
	Stimulation of Xenopus P2Y1 receptor activates CFTR in A6 cells., Guerra L., Pflugers Arch. October 1, 2004; 449 (1): 66-75.
	Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes., Chernova MN., J Physiol. May 15, 2003; 549 (Pt 1): 3-19.
	Secretory apical Cl- channels in A6 cells: possible control by cell Ca2+ and cAMP., Atia F., Pflugers Arch. August 1, 1999; 438 (3): 344-53.
	Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations., Hopf A., J Biol Chem. May 14, 1999; 274 (20): 13894-9.
	The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel., Devidas S., J Biol Chem. November 6, 1998; 273 (45): 29373-80.
	Molecular cloning and expression of a cyclic AMP-activated chloride conductance regulator: a novel ATP-binding cassette transporter., van Kuijck MA., Proc Natl Acad Sci U S A. May 28, 1996; 93 (11): 5401-6.

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