Papers associated with viscus (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.
	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.
	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.
	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.
	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.
	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.
	Regulatory interaction between CFTR and the SLC26 transporters., Shcheynikov N., Novartis Found Symp. January 1, 2006; 273 177-86; discussion 186-92, 261-4.
	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.
	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.
	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.
	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.
	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.
	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.
	Regulation of the CFTR chloride channel from humans and sharks., Hanrahan JW., J Exp Zool. July 1, 1996; 275 (4): 283-91.
	Cystic fibrosis gene encodes a cAMP-dependent chloride channel in heart., Hart P., Proc Natl Acad Sci U S A. June 25, 1996; 93 (13): 6343-8.
	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.
	Molecular cloning and expression of a cyclic AMP-activated chloride conductance regulator: a novel ATP-binding cassette transporter., van Kuijck MA., Proc Natl Acad Sci U S A. May 28, 1996; 93 (11): 5401-6.
	Mechanisms of hepatic transport and bile secretion., Erlinger S., Acta Gastroenterol Belg. January 1, 1996; 59 (2): 159-62.
	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.
	Expression of cystic fibrosis transmembrane regulator Cl- channels in heart., Levesque PC., Circ Res. October 1, 1992; 71 (4): 1002-7.

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