Papers associated with epithelium∨derBy=4 (and cftr)

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	A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development., Lee J., Sci Adv. April 7, 2023; 9 (14): eadd5745.
	CFTR supports cell death through ROS-dependent activation of TMEM16F (anoctamin 6)., Simões F., Pflugers Arch. February 1, 2018; 470 (2): 305-314.
	Hydrogen sulfide stimulates CFTR in Xenopus oocytes by activation of the cAMP/PKA signalling axis., Perniss A., Sci Rep. June 14, 2017; 7 (1): 3517.
	Mechanosensitive activation of CFTR by increased cell volume and hydrostatic pressure but not shear stress., Vitzthum C., Biochim Biophys Acta. November 1, 2015; 1848 (11 Pt A): 2942-51.
	Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.
	Influenza matrix protein 2 alters CFTR expression and function through its ion channel activity., Londino JD., Am J Physiol Lung Cell Mol Physiol. May 1, 2013; 304 (9): L582-92.
	Human trace amine-associated receptor TAAR5 can be activated by trimethylamine., Wallrabenstein I., PLoS One. January 1, 2013; 8 (2): e54950.
	Role of binding and nucleoside diphosphate kinase A in the regulation of the cystic fibrosis transmembrane conductance regulator by AMP-activated protein kinase., King JD., J Biol Chem. September 28, 2012; 287 (40): 33389-400.
	Regulation of ENaC biogenesis by the stress response protein SERP1., Faria D., Pflugers Arch. June 1, 2012; 463 (6): 819-27.
	Sildenafil acts as potentiator and corrector of CFTR but might be not suitable for the treatment of CF lung disease., Leier G., Cell Physiol Biochem. January 1, 2012; 29 (5-6): 775-90.
	The location of olfactory receptors within olfactory epithelium is independent of odorant volatility and solubility., Abaffy T., BMC Res Notes. May 6, 2011; 4 137.
	Native and recombinant Slc26a3 (downregulated in adenoma, Dra) do not exhibit properties of 2Cl-/1HCO3- exchange., Alper SL., Am J Physiol Cell Physiol. February 1, 2011; 300 (2): C276-86.
	Introduction to section V: assessment of CFTR function., Kunzelmann K., Methods Mol Biol. January 1, 2011; 741 407-18.
	Imaging CFTR in its native environment., Schillers H., Pflugers Arch. April 1, 2008; 456 (1): 163-77.
	CFTR-dependent Cl- secretion in Xenopus laevis lung epithelium., Sommer D., Respir Physiol Neurobiol. August 15, 2007; 158 (1): 97-106.
	Stable knockdown of CFTR establishes a role for the channel in P2Y receptor-stimulated anion secretion., Palmer ML., J Cell Physiol. March 1, 2006; 206 (3): 759-70.
	Regulatory interaction between CFTR and the SLC26 transporters., Shcheynikov N., Novartis Found Symp. January 1, 2006; 273 177-86; discussion 186-92, 261-4.
	Synergic action of insulin and genistein on Na+/K+/2Cl- cotransporter in renal epithelium., Ueda-Nishimura T., Biochem Biophys Res Commun. July 15, 2005; 332 (4): 1042-52.
	4-Chlorobenzo[F]isoquinoline (CBIQ), a novel activator of CFTR and DeltaF508 CFTR., Murthy M., Eur J Pharmacol. June 1, 2005; 516 (2): 118-24.
	Beta-adrenergic receptors couple to CFTR chloride channels of intercalated mitochondria-rich cells in the heterocellular toad skin epithelium., Larsen EH., Biochim Biophys Acta. December 30, 2003; 1618 (2): 140-52.
	ENaC is inhibited by an increase in the intracellular Cl(-) concentration mediated through activation of Cl(-) channels., Kunzelmann K., Pflugers Arch. January 1, 2003; 445 (4): 504-12.
	Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator., Zhang H., J Biol Chem. August 9, 2002; 277 (32): 28948-58.
	The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectrics., Dickinson P., Hum Mol Genet. February 1, 2002; 11 (3): 243-51.
	Effects of the serine/threonine kinase SGK1 on the epithelial Na(+) channel (ENaC) and CFTR: implications for cystic fibrosis., Wagner CA., Cell Physiol Biochem. January 1, 2001; 11 (4): 209-18.
	Anion permeation in Ca(2+)-activated Cl(-) channels., Qu Z., J Gen Physiol. December 1, 2000; 116 (6): 825-44.
	Potent stimulation and inhibition of the CFTR Cl(-) current by phloxine B., Bachmann A., Br J Pharmacol. October 1, 2000; 131 (3): 433-40.
	Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase., Hallows KR., J Clin Invest. June 1, 2000; 105 (12): 1711-21.
	Syntaxin 1A is expressed in airway epithelial cells, where it modulates CFTR Cl(-) currents., Naren AP., J Clin Invest. February 1, 2000; 105 (3): 377-86.
	Syntaxin 1A inhibits regulated CFTR trafficking in xenopus oocytes., Peters KW., Am J Physiol. July 1, 1999; 277 (1): C174-80.
	Downregulation of epithelial sodium channel (ENaC) by CFTR co-expressed in Xenopus oocytes is independent of Cl- conductance., Chabot H., J Membr Biol. June 1, 1999; 169 (3): 175-88.
	A divergent CFTR homologue: highly regulated salt transport in the euryhaline teleost F. heteroclitus., Singer TD., Am J Physiol. March 1, 1998; 274 (3): C715-23.
	Vasoactive intestinal peptide, forskolin, and genistein increase apical CFTR trafficking in the rectal gland of the spiny dogfish, Squalus acanthias. Acute regulation of CFTR trafficking in an intact epithelium., Lehrich RW., J Clin Invest. February 15, 1998; 101 (4): 737-45.
	Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator., Kunzelmann K., FEBS Lett. January 6, 1997; 400 (3): 341-4.
	Expression of the cystic fibrosis phenotype in a renal amphibian epithelial cell line., Ling BN., J Biol Chem. January 3, 1997; 272 (1): 594-600.
	Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator., McNicholas CM., Proc Natl Acad Sci U S A. July 23, 1996; 93 (15): 8083-8.
	Review article: new insights into the mechanisms of hepatic transport and bile secretion., Erlinger S., J Gastroenterol Hepatol. June 1, 1996; 11 (6): 575-9.
	Mechanisms of hepatic transport and bile secretion., Erlinger S., Acta Gastroenterol Belg. January 1, 1996; 59 (2): 159-62.

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