Papers associated with cftr

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	CFTR supports cell death through ROS-dependent activation of TMEM16F (anoctamin 6)., Simões F, Ousingsawat J, Wanitchakool P, Fonseca A, Cabrita I, Benedetto R, Schreiber R, Kunzelmann K., Pflugers Arch. February 1, 2018; 470 (2): 305-314.
	Retinoic acid promotes stem cell differentiation and embryonic development by transcriptionally activating CFTR., Li X, Fok KL, Guo J, Wang Y, Liu Z, Chen Z, Wang C, Ruan YC, Yu SS, Zhao H, Wu J, Jiang X, Chan HC., Biochim Biophys Acta Mol Cell Res. April 1, 2018; 1865 (4): 605-615.
	Engineered transfer RNAs for suppression of premature termination codons., Lueck JD, Yoon JS, Perales-Puchalt A, Mackey AL, Infield DT, Behlke MA, Pope MR, Weiner DB, Skach WR, McCray PB, Ahern CA., Nat Commun. February 18, 2019; 10 (1): 822.
	Cystic fibrosis drug ivacaftor stimulates CFTR channels at picomolar concentrations., Csanády L, Töröcsik B., Elife. June 17, 2019; 8
	VX-770-mediated potentiation of numerous human CFTR disease mutants is influenced by phosphorylation level., Cui G, Stauffer BB, Imhoff BR, Rab A, Hong JS, Sorscher EJ, McCarty NA., Sci Rep. September 17, 2019; 9 (1): 13460.
	Simple binding of protein kinase A prior to phosphorylation allows CFTR anion channels to be opened by nucleotides., Mihályi C, Iordanov I, Töröcsik B, Csanády L., Proc Natl Acad Sci U S A. September 1, 2020; 117 (35): 21740-21746.
	FXYD protein isoforms differentially modulate human Na/K pump function., Meyer DJ, Bijlani S, de Sautu M, Spontarelli K, Young VC, Gatto C, Artigas P., J Gen Physiol. December 7, 2020; 152 (12):
	Electrophysiological Approaches for the Study of Ion Channel Function., Cui G, Cottrill KA, McCarty NA., Methods Mol Biol. January 1, 2021; 2302 49-67.
	Clinical and molecular characterization of the R751L-CFTR mutation., Haq IJ, Althaus M, Gardner AI, Yeoh HY, Joshi U, Saint-Criq V, Verdon B, Townshend J, O'Brien C, Ben-Hamida M, Thomas M, Bourke S, van der Sluijs P, Braakman I, Ward C, Gray MA, Brodlie M., Am J Physiol Lung Cell Mol Physiol. February 1, 2021; 320 (2): L288-L300.
	UXT chaperone prevents proteotoxicity by acting as an autophagy adaptor for p62-dependent aggrephagy., Yoon MJ, Choi B, Kim EJ, Ohk J, Yang C, Choi YG, Lee J, Kang C, Song HK, Kim YK, Woo JS, Cho Y, Choi EJ, Jung H, Kim C., Nat Commun. March 29, 2021; 12 (1): 1955.
	A nonolfactory shark adenosine receptor activates CFTR with unique pharmacology and structural features., Bhanot S, Hemminger G, Martin CL, Aller SG, Forrest JN., Am J Physiol Cell Physiol. May 1, 2021; 320 (5): C892-C901.
	Molecular pathology of the R117H cystic fibrosis mutation is explained by loss of a hydrogen bond., Simon MA, Csanády L., Elife. December 6, 2021; 10
	The Effect of Dynasore Upon the Negative Interaction Between ENaC and CFTR Channels in Xenopus laevis Oocytes., Palma AG, Kotsias BA., J Membr Biol. February 1, 2022; 255 (1): 61-69.
	Oxalate secretion is stimulated by a cAMP-dependent pathway in the mouse cecum., Whittamore JM, Hatch M., Pflugers Arch. February 1, 2023; 475 (2): 249-266.
	Pharmacological inhibitors of the cystic fibrosis transmembrane conductance regulator exert off-target effects on epithelial cation channels., Lin J, Gettings SM, Talbi K, Schreiber R, Taggart MJ, Preller M, Kunzelmann K, Althaus M, Gray MA., Pflugers Arch. February 1, 2023; 475 (2): 167-179.
	A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development., Lee J, Møller AF, Chae S, Bussek A, Park TJ, Kim Y, Lee HS, Pers TH, Kwon T, Sedzinski J, Natarajan KN., Sci Adv. April 7, 2023; 9 (14): eadd5745.
	Estimating the true stability of the prehydrolytic outward-facing state in an ABC protein., Simon MA, Iordanov I, Szollosi A, Csanády L., Elife. October 2, 2023; 12

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