Papers associated with compound organ (and cftr)

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	Estimating the true stability of the prehydrolytic outward-facing state in an ABC protein., Simon MA., Elife. October 2, 2023; 12
	Oxalate secretion is stimulated by a cAMP-dependent pathway in the mouse cecum., Whittamore JM., Pflugers Arch. February 1, 2023; 475 (2): 249-266.
	A nonolfactory shark adenosine receptor activates CFTR with unique pharmacology and structural features., Bhanot S., Am J Physiol Cell Physiol. May 1, 2021; 320 (5): C892-C901.
	FXYD protein isoforms differentially modulate human Na/K pump function., Meyer DJ., J Gen Physiol. December 7, 2020; 152 (12):
	Retinoic acid promotes stem cell differentiation and embryonic development by transcriptionally activating CFTR., Li X., Biochim Biophys Acta Mol Cell Res. April 1, 2018; 1865 (4): 605-615.
	The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations., Agrawal PB., Am J Respir Cell Mol Biol. December 1, 2017; 57 (6): 711-720.
	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.
	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.
	Functional and molecular identification of a TASK-1 potassium channel regulating chloride secretion through CFTR channels in the shark rectal gland: implications for cystic fibrosis., Telles CJ., Am J Physiol Cell Physiol. December 1, 2016; 311 (6): C884-C894.
	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.
	Functional characteristics of L1156F-CFTR associated with alcoholic chronic pancreatitis in Japanese., Kondo S., Am J Physiol Gastrointest Liver Physiol. August 15, 2015; 309 (4): G260-9.
	ANP and CNP activate CFTR expressed in Xenopus laevis oocytes by direct activation of PKA., Stahl K., J Recept Signal Transduct Res. January 1, 2015; 35 (5): 493-504.
	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.
	A characterization of the Manduca sexta serotonin receptors in the context of olfactory neuromodulation., Dacks AM., PLoS One. January 1, 2013; 8 (7): e69422.
	A universally conserved residue in the SUR1 subunit of the KATP channel is essential for translating nucleotide binding at SUR1 into channel opening., de Wet H., J Physiol. October 15, 2012; 590 (20): 5025-36.
	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.
	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.
	Stimulating effect of external Myo-inositol on the expression of mutant forms of aquaporin 2., Lussier Y., J Membr Biol. July 1, 2010; 236 (2): 225-32.
	AMP-activated protein kinase phosphorylation of the R domain inhibits PKA stimulation of CFTR., King JD., Am J Physiol Cell Physiol. July 1, 2009; 297 (1): C94-101.
	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.
	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.
	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.
	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.
	Assembly and trafficking of a multiprotein ROMK (Kir 1.1) channel complex by PDZ interactions., Yoo D., J Biol Chem. February 20, 2004; 279 (8): 6863-73.
	Protein kinase-independent activation of CFTR by phosphatidylinositol phosphates., Himmel B., EMBO Rep. January 1, 2004; 5 (1): 85-90.
	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.
	Physiological modulation of CFTR activity by AMP-activated protein kinase in polarized T84 cells., Hallows KR., Am J Physiol Cell Physiol. May 1, 2003; 284 (5): C1297-308.
	Effects of purinergic stimulation, CFTR and osmotic stress on amiloride-sensitive Na+ transport in epithelia and Xenopus oocytes., Schreiber R., J Membr Biol. March 15, 2003; 192 (2): 101-10.
	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.
	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.
	No evidence for inhibition of ENaC through CFTR-mediated release of ATP., König J., Biochim Biophys Acta. September 20, 2002; 1565 (1): 17-28.
	Up-regulation of acid-gated Na(+) channels (ASICs) by cystic fibrosis transmembrane conductance regulator co-expression in Xenopus oocytes., Ji HL., J Biol Chem. March 8, 2002; 277 (10): 8395-405.
	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.
	Chromanol 293B, a blocker of the slow delayed rectifier K+ current (IKs), inhibits the CFTR Cl- current., Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. June 1, 2001; 363 (6): 590-6.

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