Papers associated with lung primordium (and cftr)

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	Engineered transfer RNAs for suppression of premature termination codons., Lueck JD., Nat Commun. February 18, 2019; 10 (1): 822.
	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.
	Counteracting suppression of CFTR and voltage-gated K+ channels by a bacterial pathogenic factor with the natural product tannic acid., Ramu Y., Elife. October 14, 2014; 3 e03683.
	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.
	Aqueous cigarette smoke extract induces a voltage-dependent inhibition of CFTR expressed in Xenopus oocytes., Moran AR., Am J Physiol Lung Cell Mol Physiol. February 1, 2014; 306 (3): L284-91.
	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.
	Characterization of SLC26A9 in patients with CF-like lung disease., Bakouh N., Hum Mutat. October 1, 2013; 34 (10): 1404-14.
	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.
	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.
	Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lung., Lazrak A., Am J Physiol Lung Cell Mol Physiol. October 1, 2011; 301 (4): L557-67.
	Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease., Azad AK., Hum Mutat. July 1, 2009; 30 (7): 1093-103.
	Characterization of SLC26A9, facilitation of Cl(-) transport by bicarbonate., Loriol C., Cell Physiol Biochem. January 1, 2008; 22 (1-4): 15-30.
	CFTR-dependent Cl- secretion in Xenopus laevis lung epithelium., Sommer D., Respir Physiol Neurobiol. August 15, 2007; 158 (1): 97-106.
	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.
	Regulatory interaction between CFTR and the SLC26 transporters., Shcheynikov N., Novartis Found Symp. January 1, 2006; 273 177-86; discussion 186-92, 261-4.
	Regulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells., Hallows KR., J Biol Chem. January 10, 2003; 278 (2): 998-1004.
	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.
	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.
	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.
	Coupled secretion of chloride and mucus in skin of Xenopus laevis: possible role for CFTR., Engelhardt JF., Am J Physiol. August 1, 1994; 267 (2 Pt 1): C491-500.

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