-
1
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan, J. R., Rommens, J. M., Kerem, B.-S., Alon, N., Rozmahel, R., Grzelczak, Z., Zielenski, J., Lok, S., Plavsic, N., Chou, J.-L. et al. (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245, 1066-1073
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.-S.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.-L.10
-
2
-
-
0026547330
-
Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia
-
Denning, G. M., Ostedgaard, L. S., Cheng, S. H., Smith, A. E. and Welsh, M. J. (1992) Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia. J. Clin. Invest. 89, 339-349
-
(1992)
J. Clin. Invest
, vol.89
, pp. 339-349
-
-
Denning, G.M.1
Ostedgaard, L.S.2
Cheng, S.H.3
Smith, A.E.4
Welsh, M.J.5
-
3
-
-
0027481813
-
The cystic fibrosis transmembrane conductance regulator
-
Riordan, J. R. (1993) The cystic fibrosis transmembrane conductance regulator. Annu. Rev. Physiol. 55, 609-630
-
(1993)
Annu. Rev. Physiol
, vol.55
, pp. 609-630
-
-
Riordan, J.R.1
-
5
-
-
0035190552
-
The CFTR-mediated protein secretion defect: Pharmacological correction
-
McPherson, M. A., Pereira, M. M. C., Russell, D., McNeilly, C. M., Morris, M. R., Stratford, F. L. L. and Dormer, R. L. (2001) The CFTR-mediated protein secretion defect: pharmacological correction. Pflügers Arch. 443 (Suppl. 1), S121-S126
-
(2001)
Pflügers Arch
, vol.443
, Issue.SUPPL. 1
-
-
McPherson, M.A.1
Pereira, M.M.C.2
Russell, D.3
McNeilly, C.M.4
Morris, M.R.5
Stratford, F.L.L.6
Dormer, R.L.7
-
6
-
-
0026951303
-
Submucosal glands are the predominant site of CFTR expression in the human bronchus
-
Engelhardt, J. F., Yankaskas, J. R., Ernst, S., Yang, Y., Marino, C. R., Boucher, R. C., Cohn, J. A. and Wilson, J. M. (1992) Submucosal glands are the predominant site of CFTR expression in the human bronchus. Nat. Genet. 2, 240-247
-
(1992)
Nat. Genet
, vol.2
, pp. 240-247
-
-
Engelhardt, J.F.1
Yankaskas, J.R.2
Ernst, S.3
Yang, Y.4
Marino, C.R.5
Boucher, R.C.6
Cohn, J.A.7
Wilson, J.M.8
-
7
-
-
0037213623
-
Role of airway surface liguid and submucosal glands in cystic fibrosis lung disease
-
Verkman, A. S., Song, Y. L. and Thiagarajah, J. R. (2003) Role of airway surface liguid and submucosal glands in cystic fibrosis lung disease. Am. J. Physiol. Cell Physiol. 284, C2-C15
-
(2003)
Am. J. Physiol. Cell Physiol
, vol.284
-
-
Verkman, A.S.1
Song, Y.L.2
Thiagarajah, J.R.3
-
8
-
-
0022478564
-
Defective β-adrenergic secretory responses in submandibular acinar cells from cystic fibrosis patients
-
McPherson, M. A., Dormer, R. L., Bradbury, N. A., Dodge, J. A. and Goodchild, M. C. (1986) Defective β-adrenergic secretory responses in submandibular acinar cells from cystic fibrosis patients. Lancet ii, 1007-1008
-
(1986)
Lancet
, vol.2
, pp. 1007-1008
-
-
McPherson, M.A.1
Dormer, R.L.2
Bradbury, N.A.3
Dodge, J.A.4
Goodchild, M.C.5
-
9
-
-
33646348165
-
Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands
-
Joo, N. S., Irokawa, T., Robbins, R. C. and Wine, J. J. (2006) Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands. J. Biol. Chem. 281, 7392-7398
-
(2006)
J. Biol. Chem
, vol.281
, pp. 7392-7398
-
-
Joo, N.S.1
Irokawa, T.2
Robbins, R.C.3
Wine, J.J.4
-
10
-
-
34347257209
-
-
Salinas, D., Haggie, P. M., Thiagarajah, J. R., Song, Y. L., Rosbe, K., Finkbeiner, W. E., Nielson, D. W. and Verkman, A. S. (2004) Submucosal gland dysfunction as a primary defect in cystic fibrosis. FASEB J. 18, NIL893-NIL905
-
Salinas, D., Haggie, P. M., Thiagarajah, J. R., Song, Y. L., Rosbe, K., Finkbeiner, W. E., Nielson, D. W. and Verkman, A. S. (2004) Submucosal gland dysfunction as a primary defect in cystic fibrosis. FASEB J. 18, NIL893-NIL905
-
-
-
-
11
-
-
0026473068
-
An antibody against a CFTR-derived synthetic peptide, incorporated into living submandibular cells, inhibits beta-adrenergic stimulation of mucin secretion
-
Lloyd Mills, C., Pereira, M. M. C., Dormer, R. L. and McPherson, M. A. (1992) An antibody against a CFTR-derived synthetic peptide, incorporated into living submandibular cells, inhibits beta-adrenergic stimulation of mucin secretion. Biochem. Biophys. Res. Commun. 188, 1146-1152
-
(1992)
Biochem. Biophys. Res. Commun
, vol.188
, pp. 1146-1152
-
-
Lloyd Mills, C.1
Pereira, M.M.C.2
Dormer, R.L.3
McPherson, M.A.4
-
13
-
-
0026581842
-
Regulation of plasma membrane recycling by CFTR
-
Bradbury, N. A., Jilling, T., Berta, G., Sorscher, E. J., Bridges, R. J. and Kirk, K. L. (1992) Regulation of plasma membrane recycling by CFTR. Science 256, 530-532
-
(1992)
Science
, vol.256
, pp. 530-532
-
-
Bradbury, N.A.1
Jilling, T.2
Berta, G.3
Sorscher, E.J.4
Bridges, R.J.5
Kirk, K.L.6
-
14
-
-
0028061411
-
Constitutive mucin secretion linked to CFTR expression
-
Kuver, R., Ramesh, N., Lau, S., Savard, C., Lee, S. P. and Osborne, W. R. A. (1994) Constitutive mucin secretion linked to CFTR expression. Biochem. Biophys. Res. Commun. 203, 1457-1462
-
(1994)
Biochem. Biophys. Res. Commun
, vol.203
, pp. 1457-1462
-
-
Kuver, R.1
Ramesh, N.2
Lau, S.3
Savard, C.4
Lee, S.P.5
Osborne, W.R.A.6
-
15
-
-
0029621143
-
CFTR gene transfer corrects defective glycoconjugate secretion in human CF epithelial tracheal cells
-
Mergey, M., Lemnaquar, M., Veissiere, D., Perricaudet, M., Gruenert, D. C., Picard, J., Capeau, J., Brahimi-Horn, M.-C. and Paul, A. (1995) CFTR gene transfer corrects defective glycoconjugate secretion in human CF epithelial tracheal cells. Am. J. Physiol. 269, L855-L864
-
(1995)
Am. J. Physiol
, vol.269
-
-
Mergey, M.1
Lemnaquar, M.2
Veissiere, D.3
Perricaudet, M.4
Gruenert, D.C.5
Picard, J.6
Capeau, J.7
Brahimi-Horn, M.-C.8
Paul, A.9
-
16
-
-
14544300522
-
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains
-
Vergani, P., Lockless, S. W., Nairn, A. C. and Gadsby, D. C. (2005) CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains. Nature 433, 876-880
-
(2005)
Nature
, vol.433
, pp. 876-880
-
-
Vergani, P.1
Lockless, S.W.2
Nairn, A.C.3
Gadsby, D.C.4
-
17
-
-
0034011511
-
PKA holoenzyme is functionally coupled to CFTR by AKAPs
-
Huang, P., Trotter, K., Boucher, R. C., Milgram, S. L. and Stutts, M. J. (2000) PKA holoenzyme is functionally coupled to CFTR by AKAPs. Am. J. Physiol. Cell Physiol. 278, C417-C422
-
(2000)
Am. J. Physiol. Cell Physiol
, vol.278
-
-
Huang, P.1
Trotter, K.2
Boucher, R.C.3
Milgram, S.L.4
Stutts, M.J.5
-
18
-
-
0029379780
-
Identification and partial characterization of a domain in CFTR that may bind cyclic nucleotides directly
-
Sullivan, S. K., Agellon, L. B. and Schick, R. (1995) Identification and partial characterization of a domain in CFTR that may bind cyclic nucleotides directly. Curr. Biol. 5, 1159-1167
-
(1995)
Curr. Biol
, vol.5
, pp. 1159-1167
-
-
Sullivan, S.K.1
Agellon, L.B.2
Schick, R.3
-
19
-
-
0033429693
-
A cyclic nucleotide PDE5 inhibitor corrects defective mucin secretion in submandibular cells containing antibody directed against the cystic fibrosis transmembrane conductance regulator protein
-
McPherson, M. A., Pereira, M. M. C., Lloyd Mills, C., Murray, K. J. and Dormer, R. L. (1999) A cyclic nucleotide PDE5 inhibitor corrects defective mucin secretion in submandibular cells containing antibody directed against the cystic fibrosis transmembrane conductance regulator protein. FEBS Lett. 464, 48-52
-
(1999)
FEBS Lett
, vol.464
, pp. 48-52
-
-
McPherson, M.A.1
Pereira, M.M.C.2
Lloyd Mills, C.3
Murray, K.J.4
Dormer, R.L.5
-
20
-
-
0347990624
-
Epac: A new cAMP-binding protein in support of glucagon-like peptide-1 receptor-mediated signal transduction in the pancreatic β-cell
-
Holz, G. G. (2004) Epac: a new cAMP-binding protein in support of glucagon-like peptide-1 receptor-mediated signal transduction in the pancreatic β-cell. Diabetes 53, 5-13
-
(2004)
Diabetes
, vol.53
, pp. 5-13
-
-
Holz, G.G.1
-
21
-
-
5344247233
-
Evidence for the involvement of cAMP-GEF (Epac) pathway in amylase release from the rat parotid gland
-
Shimomura, H., Imai, A. and Nashida, T. (2004) Evidence for the involvement of cAMP-GEF (Epac) pathway in amylase release from the rat parotid gland. Arch. Biochem. Biophys. 431, 124-128
-
(2004)
Arch. Biochem. Biophys
, vol.431
, pp. 124-128
-
-
Shimomura, H.1
Imai, A.2
Nashida, T.3
-
22
-
-
0038538404
-
Search for new cyclic AMP-binding proteins
-
Dremier, S., Kopperud, R., Doskeland, S. O., Dumont, J. E. and Maenhaut, C. (2003) Search for new cyclic AMP-binding proteins. FEBS Lett. 546, 103-107
-
(2003)
FEBS Lett
, vol.546
, pp. 103-107
-
-
Dremier, S.1
Kopperud, R.2
Doskeland, S.O.3
Dumont, J.E.4
Maenhaut, C.5
-
23
-
-
0035203949
-
Correction of delF508-CFTR activity with benzo(c)quinolizinium compounds through facilitation of its processing in cystic fibrosis airway cells
-
Dormer, R. L., Dérand, R., McNeilly, C. M., Mettey, Y., Bulteau-Pignoux, L., Vierfond, J.-M., Gray, M. A., Galietta, L. J. V., Morris, M. R., Pereira, M. M. C. et al. (2001) Correction of delF508-CFTR activity with benzo(c)quinolizinium compounds through facilitation of its processing in cystic fibrosis airway cells. J. Cell Sci. 114, 4073-4081
-
(2001)
J. Cell Sci
, vol.114
, pp. 4073-4081
-
-
Dormer, R.L.1
Dérand, R.2
McNeilly, C.M.3
Mettey, Y.4
Bulteau-Pignoux, L.5
Vierfond, J.-M.6
Gray, M.A.7
Galietta, L.J.V.8
Morris, M.R.9
Pereira, M.M.C.10
-
24
-
-
0037427513
-
Benzo(c)guinolizinium drugs inhibit degradation of F508-CFTR cytoplasmic domain
-
Stratford, F. L. L., Pereira, M. M. C., Becq, F., McPherson, M. A. and Dormer, R. L. (2003) Benzo(c)guinolizinium drugs inhibit degradation of F508-CFTR cytoplasmic domain. Biochem. Biophys. Res. Commun. 300, 524-530
-
(2003)
Biochem. Biophys. Res. Commun
, vol.300
, pp. 524-530
-
-
Stratford, F.L.L.1
Pereira, M.M.C.2
Becq, F.3
McPherson, M.A.4
Dormer, R.L.5
-
25
-
-
0032562143
-
Expression and characterization of the NBD1-R domain region of CFTR. Evidence for subunit-subunit interactions
-
Neville, D. C. A., Rozanas, C. R., Tulk, B. M., Townsend, R. R. and Verkman, A. S. (1998) Expression and characterization of the NBD1-R domain region of CFTR. Evidence for subunit-subunit interactions. Biochemistry 37, 2401-2409
-
(1998)
Biochemistry
, vol.37
, pp. 2401-2409
-
-
Neville, D.C.A.1
Rozanas, C.R.2
Tulk, B.M.3
Townsend, R.R.4
Verkman, A.S.5
-
26
-
-
0034162692
-
Cystic fibrosis transmembrane conductance regulator: The purified NBF1 + R protein interacts with the purified NBF2 domain to form a stable NBF1 + R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region
-
Lu, N. T. and Pedersen, P. L. (2000) Cystic fibrosis transmembrane conductance regulator: the purified NBF1 + R protein interacts with the purified NBF2 domain to form a stable NBF1 + R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region. Arch. Biochem. Biophys. 375, 7-20
-
(2000)
Arch. Biochem. Biophys
, vol.375
, pp. 7-20
-
-
Lu, N.T.1
Pedersen, P.L.2
-
27
-
-
0027524866
-
508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein
-
508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein. J. Biol. Chem. 268, 24330-24338
-
(1993)
J. Biol. Chem
, vol.268
, pp. 24330-24338
-
-
Ko, Y.H.1
Thomas, P.J.2
Delannoy, M.R.3
Pedersen, P.L.4
-
28
-
-
0028264035
-
Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding
-
Logan, J., Hiestand, D., Daram, P., Huang, Z., Muccio, D. D., Hartman, J., Haley, B., Cook, W. J. and Sorscher, E. J. (1994) Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding. J. Clin. Invest. 94, 228-236
-
(1994)
J. Clin. Invest
, vol.94
, pp. 228-236
-
-
Logan, J.1
Hiestand, D.2
Daram, P.3
Huang, Z.4
Muccio, D.D.5
Hartman, J.6
Haley, B.7
Cook, W.J.8
Sorscher, E.J.9
-
29
-
-
0029080926
-
Family of cyclic nucleotide gated ion channels
-
Kaupp, U. B. (1995) Family of cyclic nucleotide gated ion channels. Curr. Opin. Neurobiol. 5, 434-442
-
(1995)
Curr. Opin. Neurobiol
, vol.5
, pp. 434-442
-
-
Kaupp, U.B.1
-
30
-
-
0031006695
-
Localization and suppression of a kinetic defect in cystic fibrosis transmembrane conductance regulator folding
-
Qu, B.-H., Strickland, E. H. and Thomas, P. J. (1997) Localization and suppression of a kinetic defect in cystic fibrosis transmembrane conductance regulator folding. J. Biol. Chem. 272, 15739-15744
-
(1997)
J. Biol. Chem
, vol.272
, pp. 15739-15744
-
-
Qu, B.-H.1
Strickland, E.H.2
Thomas, P.J.3
-
31
-
-
10744230777
-
Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator
-
Lewis, H. A., Buchanan, S. G., Burley, S. K., Conners, K., Dickey, M., Dorwart, M., Fowler, R., Gao, X., Guggino, W. B., Hendrickson, W. A. et al. (2004) Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator. EMBO J. 23, 282-293
-
(2004)
EMBO J
, vol.23
, pp. 282-293
-
-
Lewis, H.A.1
Buchanan, S.G.2
Burley, S.K.3
Conners, K.4
Dickey, M.5
Dorwart, M.6
Fowler, R.7
Gao, X.8
Guggino, W.B.9
Hendrickson, W.A.10
-
32
-
-
0027179469
-
Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulator
-
Travis, S. M., Carson, M. R., Ries, D. R. and Welsh, M. J. (1993) Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulator. J. Biol. Chem. 268, 15336-15339
-
(1993)
J. Biol. Chem
, vol.268
, pp. 15336-15339
-
-
Travis, S.M.1
Carson, M.R.2
Ries, D.R.3
Welsh, M.J.4
-
33
-
-
0025931429
-
Nucleoside triphosphates are required to open the CFTR chloride channel
-
Anderson, M. P., Berger, H. A., Rich, D. P., Gregory, R. J., Smith, A. E. and Welsh, M. J. (1991) Nucleoside triphosphates are required to open the CFTR chloride channel. Cell 67, 775-784
-
(1991)
Cell
, vol.67
, pp. 775-784
-
-
Anderson, M.P.1
Berger, H.A.2
Rich, D.P.3
Gregory, R.J.4
Smith, A.E.5
Welsh, M.J.6
-
34
-
-
0026437322
-
Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding
-
Quinton, P. M. and Reddy, M. M. (1992) Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding. Nature 360, 79-81
-
(1992)
Nature
, vol.360
, pp. 79-81
-
-
Quinton, P.M.1
Reddy, M.M.2
-
35
-
-
0028070453
-
Effects of pyrophosphate and nucleoside analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator gating
-
Gunderson, K. L. and Kopito, R. R. (1994) Effects of pyrophosphate and nucleoside analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator gating. J. Biol. Chem. 269, 19349-19353
-
(1994)
J. Biol. Chem
, vol.269
, pp. 19349-19353
-
-
Gunderson, K.L.1
Kopito, R.R.2
-
36
-
-
11844254469
-
The cAMP binding domain: An ancient signaling module
-
Berman, H. M., Ten Eyck, L. F., Goodsell, D. S., Haste, N. M., Kornev, A. and Taylor, S. S. (2005) The cAMP binding domain: an ancient signaling module. Proc. Natl. Acad. Sci. U.S.A. 102, 45-50
-
(2005)
Proc. Natl. Acad. Sci. U.S.A
, vol.102
, pp. 45-50
-
-
Berman, H.M.1
Ten Eyck, L.F.2
Goodsell, D.S.3
Haste, N.M.4
Kornev, A.5
Taylor, S.S.6
-
37
-
-
0029932259
-
Active site mutations define the pathway for the cooperative activation of cAMP-dependent protein kinase
-
Herberg, F. W., Taylor, S. S. and Dostmann, W. R. G. (1996) Active site mutations define the pathway for the cooperative activation of cAMP-dependent protein kinase. Biochemistry 35, 2934-2942
-
(1996)
Biochemistry
, vol.35
, pp. 2934-2942
-
-
Herberg, F.W.1
Taylor, S.S.2
Dostmann, W.R.G.3
-
38
-
-
0024805680
-
Primary structure and functional expression from complementary DNA of the rod photoreceptor cyclic GMP-gated channel
-
Kaupp, U. B., Niidome, T., Tanabe, T., Terada, S., Bönigk, W., Stühmer, W., Cook, N., Kangawa, K., Matsuo, H., Hirose, T. et al. (1989) Primary structure and functional expression from complementary DNA of the rod photoreceptor cyclic GMP-gated channel. Nature 342, 762-766
-
(1989)
Nature
, vol.342
, pp. 762-766
-
-
Kaupp, U.B.1
Niidome, T.2
Tanabe, T.3
Terada, S.4
Bönigk, W.5
Stühmer, W.6
Cook, N.7
Kangawa, K.8
Matsuo, H.9
Hirose, T.10
-
39
-
-
0024346576
-
Predicted structure of the cGMP binding domains of the cGMP-dependent protein kinase: A key alanine/threonine difference in evolutionary divergence of cAMP and cGMP binding sites
-
Weber, I. T., Shabb, J. R. and Corbin, J. D. (1989) Predicted structure of the cGMP binding domains of the cGMP-dependent protein kinase: a key alanine/threonine difference in evolutionary divergence of cAMP and cGMP binding sites. Biochemistry 28, 6122-6127
-
(1989)
Biochemistry
, vol.28
, pp. 6122-6127
-
-
Weber, I.T.1
Shabb, J.R.2
Corbin, J.D.3
-
40
-
-
19944432524
-
Impact of the DeltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure
-
Lewis, H. A., Zhao, X., Wang, C., Sauder, J. M., Rooney, I., Noland, B. W., Lorimer, D., Kearins, M. C., Conners, K., Condon, B. et al. (2005) Impact of the DeltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure. J. Biol. Chem. 280, 1346-1353
-
(2005)
J. Biol. Chem
, vol.280
, pp. 1346-1353
-
-
Lewis, H.A.1
Zhao, X.2
Wang, C.3
Sauder, J.M.4
Rooney, I.5
Noland, B.W.6
Lorimer, D.7
Kearins, M.C.8
Conners, K.9
Condon, B.10
-
41
-
-
0037126004
-
CFTR chloride channels are regulated by a SNAP-23/syntaxin 1A complex
-
Cormet-Boyaka, E., Di, A., Chang, S. Y., Naren, A. P., Tousson, A., Nelson, D. J. and Kirk, K. L. (2002) CFTR chloride channels are regulated by a SNAP-23/syntaxin 1A complex. Proc. Natl. Acad. Sci. U.S.A. 99, 12477-12482
-
(2002)
Proc. Natl. Acad. Sci. U.S.A
, vol.99
, pp. 12477-12482
-
-
Cormet-Boyaka, E.1
Di, A.2
Chang, S.Y.3
Naren, A.P.4
Tousson, A.5
Nelson, D.J.6
Kirk, K.L.7
-
42
-
-
0032806254
-
Syntaxin 1A inhibits regulated CFTR trafficking in Xenopus oocytes
-
Peters, K. W., Qi, J. J., Watkins, S. C. and Frizzell, R. A. (1999) Syntaxin 1A inhibits regulated CFTR trafficking in Xenopus oocytes. Am. J. Physiol. Cell Physiol. 277, C174-C180
-
(1999)
Am. J. Physiol. Cell Physiol
, vol.277
-
-
Peters, K.W.1
Qi, J.J.2
Watkins, S.C.3
Frizzell, R.A.4
-
43
-
-
0033600763
-
Development of substituted benzo[c]guinolizinium compounds as novel activators of the cystic fibrosis chloride channel
-
Becq, F., Mettey, Y., Gray, M. A., Galietta, L. J. V., Dormer, R. L., Merten, M., Métayé, T., Chappe, V., Marvingt-Mounir, C., Zegarra-Moran, O. et al. (1999) Development of substituted benzo[c]guinolizinium compounds as novel activators of the cystic fibrosis chloride channel. J. Biol. Chem. 274, 27415-27425
-
(1999)
J. Biol. Chem
, vol.274
, pp. 27415-27425
-
-
Becq, F.1
Mettey, Y.2
Gray, M.A.3
Galietta, L.J.V.4
Dormer, R.L.5
Merten, M.6
Métayé, T.7
Chappe, V.8
Marvingt-Mounir, C.9
Zegarra-Moran, O.10
-
44
-
-
0031723518
-
Cystic fibrosis transmembrane conductance regulator activation by cAMP-independent mechanisms
-
He, Z. P., Raman, S., Guo, Y. and Reenstra, W. W. (1998) Cystic fibrosis transmembrane conductance regulator activation by cAMP-independent mechanisms. Am. J. Physiol. Cell Physiol. 275, C958-C966
-
(1998)
Am. J. Physiol. Cell Physiol
, vol.275
-
-
He, Z.P.1
Raman, S.2
Guo, Y.3
Reenstra, W.W.4
-
45
-
-
11944265976
-
Sildenafil (Viagra) corrects F508-CFTR location in nasal epithelial cells from cystic fibrosis patients
-
Dormer, R. L., Harris, C. M., Clark, Z., Pereira, M. M. C., Doull, I. J. M., Norez, C., Becq, F. and McPherson, M. A. (2005) Sildenafil (Viagra) corrects F508-CFTR location in nasal epithelial cells from cystic fibrosis patients. Thorax 60, 55-59
-
(2005)
Thorax
, vol.60
, pp. 55-59
-
-
Dormer, R.L.1
Harris, C.M.2
Clark, Z.3
Pereira, M.M.C.4
Doull, I.J.M.5
Norez, C.6
Becq, F.7
McPherson, M.A.8
-
46
-
-
0025242929
-
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
-
Cheng, S. H., Gregory, R. J., Marshall, J., Paul, S., Souza, D. W., White, G. A., O'Riordan, C. R. and Smith, A. E. (1990) Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 63, 827-834
-
(1990)
Cell
, vol.63
, pp. 827-834
-
-
Cheng, S.H.1
Gregory, R.J.2
Marshall, J.3
Paul, S.4
Souza, D.W.5
White, G.A.6
O'Riordan, C.R.7
Smith, A.E.8
-
47
-
-
0026753172
-
Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia
-
Denning, G. M., Ostedgaard, L. S. and Welsh, M. J. (1992) Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia. J. Cell Biol. 118, 551-559
-
(1992)
J. Cell Biol
, vol.118
, pp. 551-559
-
-
Denning, G.M.1
Ostedgaard, L.S.2
Welsh, M.J.3
|