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Summary Expression Phenotypes Gene Literature (317) GO Terms (11) Nucleotides (95) Proteins (63) Interactants (889) Wiki
XB--853971

Papers associated with cftr



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Radiotracer studies of cystic fibrosis transmembrane conductance regulator expressed in Xenopus oocytes., Ohrui T, Skach W, Thompson M, Matsumoto-Pon J, Calayag C, Widdicombe JH., Am J Physiol. June 1, 1994; 266 (6 Pt 1): C1586-93.


The substituted benzimidazolone NS004 is an opener of the cystic fibrosis chloride channel., Gribkoff VK, Champigny G, Barbry P, Dworetzky SI, Meanwell NA, Lazdunski M., J Biol Chem. April 15, 1994; 269 (15): 10983-6.


Expression of the plasmodial pfmdr1 gene in mammalian cells is associated with increased susceptibility to chloroquine., van Es HH, Karcz S, Chu F, Cowman AF, Vidal S, Gros P, Schurr E., Mol Cell Biol. April 1, 1994; 14 (4): 2419-28.


Differential acidic pH sensitivity of delta F508 CFTR Cl- channel activity in lipid bilayers., Sherry AM, Cuppoletti J, Malinowska DH., Am J Physiol. March 1, 1994; 266 (3 Pt 1): C870-5.


Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator., Smit LS, Wilkinson DJ, Mansoura MK, Collins FS, Dawson DC., Proc Natl Acad Sci U S A. November 1, 1993; 90 (21): 9963-7.


Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates., McCarty NA, McDonough S, Cohen BN, Riordan JR, Davidson N, Lester HA., J Gen Physiol. July 1, 1993; 102 (1): 1-23.


Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance., Strong TV, Wilkinson DJ, Mansoura MK, Devor DC, Henze K, Yang Y, Wilson JM, Cohn JA, Dawson DC, Frizzell RA., Hum Mol Genet. March 1, 1993; 2 (3): 225-30.


Receptors that couple to 2 classes of G proteins increase cAMP and activate CFTR expressed in Xenopus oocytes., Uezono Y, Bradley J, Min C, McCarty NA, Quick M, Riordan JR, Chavkin C, Zinn K, Lester HA, Davidson N., Recept Channels. January 1, 1993; 1 (3): 233-41.


A multifunctional aqueous channel formed by CFTR., Hasegawa H, Skach W, Baker O, Calayag MC, Lingappa V, Verkman AS., Science. November 27, 1992; 258 (5087): 1477-9.


Expression of cystic fibrosis transmembrane regulator Cl- channels in heart., Levesque PC, Hart PJ, Hume JR, Kenyon JL, Horowitz B., Circ Res. October 1, 1992; 71 (4): 1002-7.


Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive., Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ., Nature. August 27, 1992; 358 (6389): 761-4.


Identification and developmental expression of the Xenopus laevis cystic fibrosis transmembrane conductance regulator gene., Tucker SJ, Tannahill D, Higgins CF., Hum Mol Genet. May 1, 1992; 1 (2): 77-82.


cAMP-stimulated ion currents in Xenopus oocytes expressing CFTR cRNA., Cunningham SA, Worrell RT, Benos DJ, Frizzell RA., Am J Physiol. March 1, 1992; 262 (3 Pt 1): C783-8.


CFTR protein expression in primary and cultured epithelia., Zeitlin PL, Crawford I, Lu L, Woel S, Cohen ME, Donowitz M, Montrose MH, Hamosh A, Cutting GR, Gruenert D., Proc Natl Acad Sci U S A. January 1, 1992; 89 (1): 344-7.


Chloride conductance expressed by delta F508 and other mutant CFTRs in Xenopus oocytes., Drumm ML, Wilkinson DJ, Smit LS, Worrell RT, Strong TV, Frizzell RA, Dawson DC, Collins FS., Science. December 20, 1991; 254 (5039): 1797-9.


Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene., Bear CE, Duguay F, Naismith AL, Kartner N, Hanrahan JW, Riordan JR., J Biol Chem. October 15, 1991; 266 (29): 19142-5.


Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients., Dean M, White MB, Amos J, Gerrard B, Stewart C, Khaw KT, Leppert M., Cell. June 1, 1990; 61 (5): 863-70.

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