Papers associated with multi-tissue structure (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.
	Oxalate secretion is stimulated by a cAMP-dependent pathway in the mouse cecum., Whittamore JM., Pflugers Arch. February 1, 2023; 475 (2): 249-266.
	Engineered transfer RNAs for suppression of premature termination codons., Lueck JD., Nat Commun. February 18, 2019; 10 (1): 822.
	Molecular Structure of the Human CFTR Ion Channel., Liu F., Cell. March 23, 2017; 169 (1): 85-95.e8.
	Loss of Cystic Fibrosis Transmembrane Regulator Impairs Intestinal Oxalate Secretion., Knauf F., J Am Soc Nephrol. January 1, 2017; 28 (1): 242-249.
	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.
	Obligate coupling of CFTR pore opening to tight nucleotide-binding domain dimerization., Mihályi C., Elife. June 21, 2016; 5
	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.
	Structure-activity analysis of a CFTR channel potentiator: Distinct molecular parts underlie dual gating effects., Csanády L., J Gen Physiol. October 1, 2014; 144 (4): 321-36.
	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.
	Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR., Cui G., J Gen Physiol. August 1, 2014; 144 (2): 159-79.
	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.
	Catalyst-like modulation of transition states for CFTR channel opening and closing: new stimulation strategy exploits nonequilibrium gating., Csanády L., J Gen Physiol. February 1, 2014; 143 (2): 269-87.
	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.
	A characterization of the Manduca sexta serotonin receptors in the context of olfactory neuromodulation., Dacks AM., PLoS One. January 1, 2013; 8 (7): e69422.
	Regional differences in rat conjunctival ion transport activities., Yu D., Am J Physiol Cell Physiol. October 1, 2012; 303 (7): C767-80.
	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.
	Contribution of casein kinase 2 and spleen tyrosine kinase to CFTR trafficking and protein kinase A-induced activity., Luz S., Mol Cell Biol. November 1, 2011; 31 (22): 4392-404.
	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.
	SLC26 anion exchangers of guinea pig pancreatic duct: molecular cloning and functional characterization., Stewart AK., Am J Physiol Cell Physiol. August 1, 2011; 301 (2): C289-303.
	ERp29 regulates DeltaF508 and wild-type cystic fibrosis transmembrane conductance regulator (CFTR) trafficking to the plasma membrane in cystic fibrosis (CF) and non-CF epithelial cells., Suaud L., J Biol Chem. June 17, 2011; 286 (24): 21239-53.
	Mutant cycles at CFTR's non-canonical ATP-binding site support little interface separation during gating., Szollosi A., J Gen Physiol. June 1, 2011; 137 (6): 549-62.
	Involvement of F1296 and N1303 of CFTR in induced-fit conformational change in response to ATP binding at NBD2., Szollosi A., J Gen Physiol. October 1, 2010; 136 (4): 407-23.
	Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct., Lu M., Proc Natl Acad Sci U S A. March 30, 2010; 107 (13): 6082-7.
	Metformin treatment of diabetes mellitus increases the risk for pancreatitis in patients bearing the CFTR-mutation S573C., Kongsuphol P., Cell Physiol Biochem. January 1, 2010; 25 (4-5): 389-96.
	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.
	Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTR., Treharne KJ., Cell Physiol Biochem. January 1, 2009; 24 (5-6): 347-60.
	Regulation of CFTR trafficking by its R domain., Lewarchik CM., J Biol Chem. October 17, 2008; 283 (42): 28401-12.
	The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct., Shcheynikov N., J Physiol. August 15, 2008; 586 (16): 3813-24.
	Mutations at arginine 352 alter the pore architecture of CFTR., Cui G., J Membr Biol. March 1, 2008; 222 (2): 91-106.
	The role of SGK and CFTR in acute adaptation to seawater in Fundulus heteroclitus., Shaw JR., Cell Physiol Biochem. January 1, 2008; 22 (1-4): 69-78.
	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.
	Shark rectal gland vasoactive intestinal peptide receptor: cloning, functional expression, and regulation of CFTR chloride channels., Bewley MS., Am J Physiol Regul Integr Comp Physiol. October 1, 2006; 291 (4): R1157-64.
	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.
	Regulatory interaction between CFTR and the SLC26 transporters., Shcheynikov N., Novartis Found Symp. January 1, 2006; 273 177-86; discussion 186-92, 261-4.
	Preferential phosphorylation of R-domain Serine 768 dampens activation of CFTR channels by PKA., Csanády L., J Gen Physiol. February 1, 2005; 125 (2): 171-86.
	Functional roles of nonconserved structural segments in CFTR's NH2-terminal nucleotide binding domain., Csanády L., J Gen Physiol. January 1, 2005; 125 (1): 43-55.
	Potentiation of effect of PKA stimulation of Xenopus CFTR by activation of PKC: role of NBD2., Chen Y., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1436-44.
	Inhibition of CFTR channels by a peptide toxin of scorpion venom., Fuller MD., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1328-41.
	Mechanism of activation of Xenopus CFTR by stimulation of PKC., Chen Y., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1256-63.
	Stimulation of Xenopus P2Y1 receptor activates CFTR in A6 cells., Guerra L., Pflugers Arch. October 1, 2004; 449 (1): 66-75.
	Involvement of G protein betagamma-subunits in diverse signaling induced by G(i/o)-coupled receptors: study using the Xenopus oocyte expression system., Uezono Y., Am J Physiol Cell Physiol. October 1, 2004; 287 (4): C885-94.
	Dynamic control of cystic fibrosis transmembrane conductance regulator Cl(-)/HCO3(-) selectivity by external Cl(-)., Shcheynikov N., J Biol Chem. May 21, 2004; 279 (21): 21857-65.

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