Papers associated with lung (and camp)

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	δβγ-ENaC is inhibited by CFTR but stimulated by cAMP in Xenopus laevis oocytes., Rauh R., Am J Physiol Lung Cell Mol Physiol. February 1, 2017; 312 (2): L277-L287.
	Hydrogen sulfide decreases β-adrenergic agonist-stimulated lung liquid clearance by inhibiting ENaC-mediated transepithelial sodium absorption., Agné AM., Am J Physiol Regul Integr Comp Physiol. April 1, 2015; 308 (7): R636-49.
	Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability., Liu X., Biochemistry. September 9, 2014; 53 (35): 5613-8.
	Inter-α-inhibitor blocks epithelial sodium channel activation and decreases nasal potential differences in ΔF508 mice., Lazrak A., Am J Respir Cell Mol Biol. May 1, 2014; 50 (5): 953-62.
	Neurulation and neurite extension require the zinc transporter ZIP12 (slc39a12)., Chowanadisai W., Proc Natl Acad Sci U S A. June 11, 2013; 110 (24): 9903-8.
	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.
	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.
	Cpt-cAMP activates human epithelial sodium channels via relieving self-inhibition., Molina R., Biochim Biophys Acta. July 1, 2011; 1808 (7): 1818-26.
	CASZ1b, the short isoform of CASZ1 gene, coexpresses with CASZ1a during neurogenesis and suppresses neuroblastoma cell growth., Liu Z., PLoS One. April 7, 2011; 6 (4): e18557.
	Characterization of SLC26A9, facilitation of Cl(-) transport by bicarbonate., Loriol C., Cell Physiol Biochem. January 1, 2008; 22 (1-4): 15-30.
	Cloning and activation of the bullfrog apelin receptor: Gi/o coupling and high affinity for [Pro1]apelin-13., Moon MJ., Mol Cell Endocrinol. October 15, 2007; 277 (1-2): 51-60.
	An extract from the medicinal plant Phyllanthus acidus and its isolated compounds induce airway chloride secretion: A potential treatment for cystic fibrosis., Sousa M., Mol Pharmacol. January 1, 2007; 71 (1): 366-76.
	Characterization of the cloned guinea pig leukotriene B4 receptor: comparison to its human orthologue., Boie Y., Eur J Pharmacol. September 10, 1999; 380 (2-3): 203-13.
	cDNA cloning and characterization of guinea-pig leukotriene B4 receptor., Masuda K., Biochem J. August 15, 1999; 342 ( Pt 1) 79-85.
	Cystic fibrosis transmembrane conductance regulator-associated ATP release is controlled by a chloride sensor., Jiang Q., J Cell Biol. November 2, 1998; 143 (3): 645-57.
	Identification, functional characterization, and developmental expression of two nonallelic parathyroid hormone (PTH)/PTH-related peptide receptor isoforms in Xenopus laevis (Daudin)., Bergwitz C., Endocrinology. February 1, 1998; 139 (2): 723-32.
	Sequence and expression analysis of a Xenopus laevis cDNA which encodes a homologue of mammalian 14-3-3 zeta protein., Kousteni S., Gene. May 6, 1997; 190 (2): 279-85.
	Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease., Steinmeyer K., J Biol Chem. December 29, 1995; 270 (52): 31172-7.
	Molecular and functional characterization of a partial cDNA encoding a novel chicken brain melatonin receptor., Liu F., FEBS Lett. October 30, 1995; 374 (2): 273-8.
	Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents., Fulmer SB., Proc Natl Acad Sci U S A. July 18, 1995; 92 (15): 6832-6.
	Molecular cloning and characterization of an aquaporin cDNA from salivary, lacrimal, and respiratory tissues., Raina S., J Biol Chem. January 27, 1995; 270 (4): 1908-12.
	Cloning, functional expression, and characterization of the human prostaglandin E2 receptor EP2 subtype., Bastien L., J Biol Chem. April 22, 1994; 269 (16): 11873-7.
	Cloning and expression of a cDNA for the human prostanoid IP receptor., Boie Y., J Biol Chem. April 22, 1994; 269 (16): 12173-8.
	Evidence for apical sodium channels in frog lung epithelial cells., Fischer H., Am J Physiol. April 1, 1989; 256 (4 Pt 1): C764-71.

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