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123bio.net - Revues - La mucoviscidose http://www.123bio.net/revues/vchappe/biblio.html Page 1 of 9 3/27/2009 accueil > revues > la mucoviscidose La mucoviscidose. Auteur : Dr. Valérie CHAPPE McGill University, McIntyre Medical Sciences Building, Dept. of Physiology, Montréal, Québec, Canada. RÉFÉRENCES BIBLIOGRAPHIQUES : Abbracchio MP & Burnstock G (1998). Purinergic signalling: pathophysiological roles. Jpn J of Pharmacol 78:113- 145. Akabas MH, Cheung M & Guinamard R (1997). Probing the structural and functional domains of the CFTR chloride channel. J Bioenerg Biomembr 29:453-463. Akabas MH, Kaufmann C, Cook TA & Archdeacon (1994). Amino acid residues lining the chloride channel of the Cystic Fibrosis Transmembrane conductance regulator. J Biol Chem 269 14865-14868. Allert N, Leipziger J & Greger R (1992). cAMP and Ca2+ act co-operatively on the Cl- conductance of HT29 cells. Pflügers Arch 421:403-405. Annereau J-P, Stoven V, Bontems F, Barthe J, Lenoir G, Blanquet S & Lallemand J-Y (1997a). Insight into cystic fibrosis by structural modelling of CFTR first nucleotide binding fold (NBF1). CR Acad Sci Paris 320:113 -121. Annereau J-P, Wulbrand U, Vankeerberghen A, Cuppens H, Bontems F, Tümmler B, Cassiman J-J & Stoven V (1997b). A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator. FEBS Letters 407:303-308. Arispe N, Ma J, Jacobson KA & Pollard HB (1998). Direct activation of cystic fibrosis transmembrane conductance regulator channel by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX). J Biol Chem 273:5727-5734. Arispe N, Rojas E, Hartman J, Sorscher EJ & Pollard HB (1992). Intrinsic anion channel activity of the recombinant first nucleotide binding fold of the cystic fibrosis transmembrane regulator protein. Proc Natl Acad Sci USA 89:1539- 43. Baichwal V, Liu D & Ames GF (1993). The ATP-binding component of a prokaryotic traffic ATPase is exposed to the periplasmic (external) surface. Proc Natl Acad Sci USA 90:620-4. Bear CE, Duguay F, Naismith AL, Kartner N, Hanrahan JW & Riordan JR (1991). Cl- channel activity in Xenopus oocytes expressing the cystic fibbrosis gene. J Biol Chem 266:19142-5. Becq F, Fanjul M, Mahieu I, Berger Z, Gola & Hollande E (1992). Anion channels in a human pancreatic cancer cell line (Capan-1) of ductal origin. Pflügers Arch 420:46-53. Becq F, Hollande E & Gola M (1993). Phosphorylation-regulated low-conductance Cl- channels in a human pancreatic duct cell line. Pflügers Arch 425:1-8. Becq F, Verrier B , Chang X-B, Riordan JR & Hanrahan JW (1996). cAMP- and Ca2+-independent activation of cystic fibrosis transmembrane conductance regulator channel by phenylimidazothiazole drugs. J Biol Chem 271:16171-16179. Becq F, Jensen TJ, Chang X-B, Savoia A, Rommens JM, Tsui L-C, Buchwald M, Riordan JR & Hanrahan JW (1994). Phosphatase inhibitors activate normal and defective CFTR chloride channels. Proc Natl Acad Sci USA 91:9160-9164. Benharouga M, Fritsch J, Banting G & Edelman A (1997). Properties of chloride-conductive pathways in rat kidney
123bio.net - Revues - La mucoviscidose http://www.123bio.net/revues/vchappe/biblio.html Page 2 of 9 3/27/2009 cortical and outer-medulla brush border membranes. Inhibition by anti-(cystic fibrosis transmembrane conductance regulator)mAbs. Eur J Biochem 246:367-72. Bianchet MA, Ko YH, Amzel LM & Pedersen PL (1997). Modeling of nucleotide binding domains of ABC transporter proteins based on a F1-ATPase/recA topology: Structural model of the nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator (CFTR). J Bioenerg Biomemb 29:503-524. Biwersi J, Emans N & Verkman AS (1996). Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo. Proc Natl Acad Sci USA 93:12484-12489. Biwersi J & Verkman AS (1994). Functional CFTR in endosomal compartment of CFTR-expressing fibroblasts and T84 cells. Am J Physiol 35:C149-C156. Bizzarri C & Corda D (1994). Norepinephrine, unlike ATP, induces all-or-none increase in cytosolic calcium in thyroid cells. Eur J Biochem 219:837-844. Bradbury NA, Cohn JA, Venglarik CJ & Bridges RJ (1994). Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles. J Biol Chem 269:8296-8302. Bradbury NA, Jilling T, Berta G, Sorscher EJ, Bridges RJ, Kirk KL (1992). Regulation of plasma membrane recycling by CFTR. Science 256:530-531. Cantiello HF (1996). Physiological society symposium: ion transport in health and disease. Role of the actin cytoskeleton in the regulation of the cystic fibrosis transmembrane conductance regulator. Exper Physiol 81:505- 514. Cantiello HF (1997). Nucleotide transport through the cystic fibrosis transmembrane conductance regulator. Bioscience Reports 17:147-171. Cantiello HF, Prat AG, Reisin IL, Ercole LB, Abraham EH, Amara JF, Gregory RJ & Ausiello DA (1994). External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism. J Biol Chem 269:11224-32. Caplan MJ (1997). Pumps in epithelial cells : sorting, stabilization, and polarity. Am J Physiol 272:G1304-13. Carrasco N (1993). Iodide transport in the thyroid gland. Biochem Biophys Acta 1154:65-82. Chan HC, Cheung WT, Leung PY, Wu LJ, Cheng Chew SB, Ko WH & Wong PYD (1996). Purinergic regulation of anion secretion by cystic fibrosis pancreatic duct cells. Am J Physiol 271:C469-C477. Chan HC, Liu CQ, Fong SK, Law SH, Wu LJ, So E, Chung YW, Ko WH, Wong PYD (1997). Regulation of Clsecretion by extracellular ATP in cultured mouse endometrial epithelium. J Memb Biol 156:45-52. Chang X-B, Kartner N, Seibert FS, Aleksandrov AA, Kloser AW, Kiser GL & Riordan JR (1998). Heterologous expression systems for study of cystic fibrosis transmembrane conductance regulator. Meth Enzymol 292:616-629. Chao AC, Kouyama K, Heist EK, Dong Y-J & Gardner P (1995). Calcium- and CaMKII-dependent chloride secretion induced by the microsomal Ca2+-ATPase inhibitor 2,5-Di-(tert-butyl)-a,4-hydroquinone in cystic fibrosis pancreatic epithelial cells. J Clin Invest 96 :1794-1801. Chappe V, Mettey Y, Vierfond JM, Hanrahan JW, Gola M, Verrier B & Becq F (1998). Structural basis for specificity and potency of xanthine derivatives as activators of the CFTR chloride channel. Br J Pharmacol 123:683-693. Chen M & Zhang J-T (1996). Membrane insertion, processing, and topology of cystic fibrosis transmembrane conductance regulator (CFTR) in microsomal membranes. Mol Memb Biol 13:33-40. Clancy JP, Bebök ZS & Sorscher EJ (1997). Purification, characterization, and expression of CFTR nucleotidebinding domains. J Bioenerg Biomembr 29:475-482. Cohen BE, Lee G, Jacobson KA, Kim Y-C, Huang Z, Sorscher EJ & Pollard HB (1997). 8-cyclopentyl-1,3- dipropylxanthine and other xanthines differentially bind to the wild-type and ΔF508 mutant first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator. Biochemistry 36:6455-6461.
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