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Julien M, Verrier B, Cerutti M, Chappe V, Gola M, Devauchelle G & Becq F (1999). Cystic fibrosis transmembrane
conductance regulator (CFTR) confers glibenclamide-sensitivity to outwardly rectifying chloride channel (ORCC) in
Hi-5 insect cells. J Membr Biol 168: 229-239.
Kelley TJ, al Nakkash L & Drumm ML (1995). CFTR-mediated chloide permeability is regulated by type III
phosphodiesterases in airway epithelial cells. Am J Respir Cell Mol Biol 13:657-64.
Kelley TJ, Thomas K, Milgram LJH & Drumm ML (1997). In vivo activation of the cystic fibrosis transmembrane
conductance regulator mutant DF508 in murine nasal epithelium. Proc Natl Acad Sci 94:2604-2608.
Kopito RR (1999). Biosynthesis and degradation of CFTR. Physiol Rev 79:S167-S173.
Laglia G, Zeiger MA, Leipricht A, Caturegli P, Levine MA, Kohn LD & Saji M (1996). Increased cyclic adenosine 3',
5'-monophosphate inhibits G protein-coupled activation of phospholipase C in rat FRTL-5 thyroid cells.
Endocrinology 137:3170-3176.
Li C, Ramjeesingh M & Bear CE (1996b). Purified cystic fibrosis transmembrane conductance regulator (CFTR)
does not function as an ATP channel. J Biol Chem 271:11623-6.
Liedtke CM & Cole TS (1998). Antisense oligonucleotide to PKC-epsilon alters cAMP-dependent stimulation of
CFTR in Calu-3 cells. Am J Physiol 275 :C1357-64.
Linsdell P & Hanrahan JW (1998a). Glutathione permeability of CFTR. Am J Physiol 275:C323-C326.
Linsdell P & Hanrahan JW (1998b). Adenosine triphosphate-dependent asymmetry of anion permeation in the
cystic fibrosis transmembrane conductance regulator chloride channel. J Gen Physiol 111:601-14.
Linsdell P, Tabcharani JA & Hanrahan JW (1997a). Multi-ion mechanism for ion permeation and block in the cystic
fibrosis transmembrane conductance regulator chloride channel. J Gen Physiol 110:365-377.
Linsdell P, Tabcharani JA, Rommens JM, Hou Y-X, Chang X-B, Tsui L-C, Riordan JR & Hanrahan JW (1997b).
Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to
polyatomic anions. J Gen Physiol 110: 355-364.
Linsdell P, Sheng S-X & Hanrahan JW (1998c). Non-pore lining amino acid side chains influence anion selectivity of
the human CFTR Cl- channel expressed in mammalian cell lines. J Physiol 512:1-16.
Luo J, Pato MD, Riordan JR & Hanrahan JW (1998). Differential regulation of single CFTR channels by PP2C,
PP2A, and other phosphatases. Am J Physiol 274 :C1397-410.
Loussouarn G, Demolombe S, Mohammad Panah R, Escande D & Baró I (1996). Expression of CFTR controls
cAMP-dependent activation of epithelial K+ currents. Am J Physiol 271:C1565-73.
Mall M, Bleich M, Greger R, Schreiber R & Kunzelmann K (1998). The amiloride-inhibitable Na+ conductance is
reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways. J
Clin Invest 102 :15-21.
Martin SC (1992). ATP activated a Ca2+-dependent Cl- current in the rat thyroid cell line, FRTL-5. J Membr Biol
125:243-253.
Marunaka Y (1993). Modification of Ca2+ sensitivity of Ca2+-activated Cl- channel by vasopressin and cholera
toxin. Jp J Physiol 43:553-560.
Mathews CJ, Tabcharani JA, Chang X-B, Jensen TJ, Riordan JR & Hanrahan JW (1998). Dibasic protein kinase A
sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator
chloride channel. J Physiol 508:365-377.
McCarthy NA, McDonough S, Cohen BN, Riordan JR, Davidson N & Lester HA (1993). Voltage-dependent block of
the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates. J
Gen Physiol 102:1-23.
McDonough S, Davidson N, Lester HA & McCarty NA (1994). Novel pore-lining residues in CFTR that govern
permeation and open-channel block. Neuron 13:623-634.