-
1
-
-
0035141190
-
A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs
-
Al Nakkash L, Hu S, Li M, Hwang TC. A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs. J Pharmacol Exp Ther 296: 464-472, 2001.
-
(2001)
J Pharmacol Exp Ther
, vol.296
, pp. 464-472
-
-
Al Nakkash, L.1
Hu, S.2
Li, M.3
Hwang, T.C.4
-
4
-
-
0028323310
-
Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→G
-
Bozon D, Zielenski J, Rininsland F, Tsui LC. Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→G. Hum Mutat 3: 330-332, 1994.
-
(1994)
Hum Mutat
, vol.3
, pp. 330-332
-
-
Bozon, D.1
Zielenski, J.2
Rininsland, F.3
Tsui, L.C.4
-
5
-
-
0035794120
-
Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation
-
Braunstein GM, Roman RM, Clancy JP, Kudlow BA, Taylor AL, Shylonsky VG, Jovov B, Peter K, Jilling T, Ismailov II, Benos DJ, Schwiebert LM, Fitz JG, Schwiebert EM. Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation. J Biol Chem 276: 6621-6630, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 6621-6630
-
-
Braunstein, G.M.1
Roman, R.M.2
Clancy, J.P.3
Kudlow, B.A.4
Taylor, A.L.5
Shylonsky, V.G.6
Jovov, B.7
Peter, K.8
Jilling, T.9
Ismailov, I.I.10
Benos, D.J.11
Schwiebert, L.M.12
Fitz, J.G.13
Schwiebert, E.M.14
-
6
-
-
0031921269
-
+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC
-
+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC. J Physiol 508: 825-836, 1998.
-
(1998)
J Physiol
, vol.508
, pp. 825-836
-
-
Briel, M.1
Greger, R.2
Kunzelmann, K.3
-
7
-
-
0038799725
-
Structure of MsbA from Vibrio cholera: A multidrug resistance ABC transporter homolog in a closed conformation
-
Chang G. Structure of MsbA from Vibrio cholera: a multidrug resistance ABC transporter homolog in a closed conformation. J Mol Biol 330: 419-430, 2003.
-
(2003)
J Mol Biol
, vol.330
, pp. 419-430
-
-
Chang, G.1
-
8
-
-
0035823075
-
Structure of MsbA from E. coli: A homolog of the multidrug resistance ATP binding cassette (ABC) transporters
-
Chang G, Roth CB. Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette (ABC) transporters. Science 293: 1793-1800, 2001.
-
(2001)
Science
, vol.293
, pp. 1793-1800
-
-
Chang, G.1
Roth, C.B.2
-
10
-
-
26444542440
-
Are p.I148T, p.R74W, and p.D1270N cystic fibrosis causing mutations?
-
Claustres M, Altieri JP, Guittard C, Templin C, Chevalier-Porst F, des GM. Are p.I148T, p.R74W, and p.D1270N cystic fibrosis causing mutations? BMC Med Genet 5: 19, 2004.
-
(2004)
BMC Med Genet
, vol.5
, pp. 19
-
-
Claustres, M.1
Altieri, J.P.2
Guittard, C.3
Templin, C.4
Chevalier-Porst, F.5
des, G.M.6
-
13
-
-
0032743305
-
Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein
-
Illek B, Zhang L, Lewis NC, Moss RB, Dong JY, Fischer H. Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein. Am J Physiol Cell Physiol 277: C833-C839, 1999.
-
(1999)
Am J Physiol Cell Physiol
, vol.277
-
-
Illek, B.1
Zhang, L.2
Lewis, N.C.3
Moss, R.B.4
Dong, J.Y.5
Fischer, H.6
-
14
-
-
0029912194
-
Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator
-
Ismailov II, Awayda MS, Jovov B, Berdiev BK, Fuller CM, Dedman JR, Kaetzel M, Benos DJ. Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator. J Biol Chem 271: 4725-4732, 1996.
-
(1996)
J Biol Chem
, vol.271
, pp. 4725-4732
-
-
Ismailov, I.I.1
Awayda, M.S.2
Jovov, B.3
Berdiev, B.K.4
Fuller, C.M.5
Dedman, J.R.6
Kaetzel, M.7
Benos, D.J.8
-
15
-
-
0034623128
-
The cytosolic termini of the β- and γ-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel
-
Ji HL, Chalfant ML, Jovov B, Lockhart JP, Parker SB, Fuller CM, Stanton BA, Benos DJ. The cytosolic termini of the β- and γ-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel. J Biol Chem 275: 27947-27956, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 27947-27956
-
-
Ji, H.L.1
Chalfant, M.L.2
Jovov, B.3
Lockhart, J.P.4
Parker, S.B.5
Fuller, C.M.6
Stanton, B.A.7
Benos, D.J.8
-
16
-
-
0034607827
-
Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes
-
Jiang Q, Li J, Dubroff R, Ahn YJ, Foskett JK, Engelhardt J, Kleyman TR. Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes. J Biol Chem 275: 13266-13274, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 13266-13274
-
-
Jiang, Q.1
Li, J.2
Dubroff, R.3
Ahn, Y.J.4
Foskett, J.K.5
Engelhardt, J.6
Kleyman, T.R.7
-
17
-
-
0036194724
-
Mucus clearance as a primary innate defense mechanism for mammalian airways
-
Knowles MR, Boucher RC. Mucus clearance as a primary innate defense mechanism for mammalian airways. J Clin Invest 109: 571-577, 2002.
-
(2002)
J Clin Invest
, vol.109
, pp. 571-577
-
-
Knowles, M.R.1
Boucher, R.C.2
-
20
-
-
0031024767
-
+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator
-
+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator. FEBS Lett 400: 341-344, 1997.
-
(1997)
FEBS Lett
, vol.400
, pp. 341-344
-
-
Kunzelmann, K.1
Kiser, G.L.2
Schreiber, R.3
Riordan, J.R.4
-
22
-
-
0037052565
-
The E. coli BtuCD structure: A framework for ABC transporter architecture and mechanism
-
Locher KP, Lee AT, Rees DC. The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism. Science 296: 1091-1098, 2002.
-
(2002)
Science
, vol.296
, pp. 1091-1098
-
-
Locher, K.P.1
Lee, A.T.2
Rees, D.C.3
-
24
-
-
14544294477
-
ClC-5 chloride channel alters expression of the epithelial sodium channel (ENaC)
-
Mo L, Wills NK. ClC-5 chloride channel alters expression of the epithelial sodium channel (ENaC). J Membr Biol 202: 21-37, 2004.
-
(2004)
J Membr Biol
, vol.202
, pp. 21-37
-
-
Mo, L.1
Wills, N.K.2
-
25
-
-
18944361982
-
CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes
-
Nagel G, Barbry P, Chabot H, Brochiero E, Hartung K, Grygorczyk R. CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes. J Physiol 564: 671-682, 2005.
-
(2005)
J Physiol
, vol.564
, pp. 671-682
-
-
Nagel, G.1
Barbry, P.2
Chabot, H.3
Brochiero, E.4
Hartung, K.5
Grygorczyk, R.6
-
26
-
-
0035065745
-
Non-specific activation of the epithelial sodium channel by the CFTR chloride channel
-
Nagel G, Szellas T, Riordan JR, Friedrich T, Hartung K. Non-specific activation of the epithelial sodium channel by the CFTR chloride channel. EMBO Rep 2: 249-254, 2001.
-
(2001)
EMBO Rep
, vol.2
, pp. 249-254
-
-
Nagel, G.1
Szellas, T.2
Riordan, J.R.3
Friedrich, T.4
Hartung, K.5
-
27
-
-
0033562963
-
Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein
-
Randak C, Auerswald EA, Assfalg-Machleidt I, Reenstra WW, Machleidt W. Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein. Biochem J 340: 227-235, 1999.
-
(1999)
Biochem J
, vol.340
, pp. 227-235
-
-
Randak, C.1
Auerswald, E.A.2
Assfalg-Machleidt, I.3
Reenstra, W.W.4
Machleidt, W.5
-
29
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL, Drumm ML, Iannuzzi MC, Collins FS, Tsui LC. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245: 1066-1073, 1989.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.L.10
Drumm, M.L.11
Iannuzzi, M.C.12
Collins, F.S.13
Tsui, L.C.14
-
31
-
-
0028980536
-
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP
-
Schwiebert EM, Egan ME, Hwang TH, Fulmer SB, Allen SS, Cutting GR, Guggino WB. CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP. Cell 81: 1063-1073, 1995.
-
(1995)
Cell
, vol.81
, pp. 1063-1073
-
-
Schwiebert, E.M.1
Egan, M.E.2
Hwang, T.H.3
Fulmer, S.B.4
Allen, S.S.5
Cutting, G.R.6
Guggino, W.B.7
-
32
-
-
0030775639
-
Disease-associated mutations in cytoplasmic loops 1 and 2 of cystic fibrosis transmembrane conductance regulator impede processing or opening of the channel
-
Seibert FS, Jia Y, Mathews CJ, Hanrahan JW, Riordan JR, Loo TW, Clarke DM. Disease-associated mutations in cytoplasmic loops 1 and 2 of cystic fibrosis transmembrane conductance regulator impede processing or opening of the channel. Biochemistry 36: 11966-11974, 1997.
-
(1997)
Biochemistry
, vol.36
, pp. 11966-11974
-
-
Seibert, F.S.1
Jia, Y.2
Mathews, C.J.3
Hanrahan, J.W.4
Riordan, J.R.5
Loo, T.W.6
Clarke, D.M.7
-
33
-
-
0347927706
-
Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes
-
Suaud L, Carattino M, Kleyman TR, Rubenstein RC. Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes. J Biol Chem 277: 50341-50347, 2002.
-
(2002)
J Biol Chem
, vol.277
, pp. 50341-50347
-
-
Suaud, L.1
Carattino, M.2
Kleyman, T.R.3
Rubenstein, R.C.4
-
34
-
-
0037088577
-
Genistein restores functional interactions between ΔF508-CFTR and ENaC in Xenopus oocytes
-
Suaud L, Li J, Jiang Q, Rubenstein RC, Kleyman TR. Genistein restores functional interactions between ΔF508-CFTR and ENaC in Xenopus oocytes. J Biol Chem 277: 8928-8933, 2002.
-
(2002)
J Biol Chem
, vol.277
, pp. 8928-8933
-
-
Suaud, L.1
Li, J.2
Jiang, Q.3
Rubenstein, R.C.4
Kleyman, T.R.5
-
35
-
-
0030029948
-
Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel
-
Tao T, Xie J, Drumm ML, Zhao J, Davis PB, Ma J. Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel. Biophys J 70: 743-753, 1996.
-
(1996)
Biophys J
, vol.70
, pp. 743-753
-
-
Tao, T.1
Xie, J.2
Drumm, M.L.3
Zhao, J.4
Davis, P.B.5
Ma, J.6
-
36
-
-
0030818110
-
Direct action of genistein on CFTR
-
Weinreich F, Wood PG, Riordan JR, Nagel G. Direct action of genistein on CFTR. Pflügers Arch 434: 484-491, 1997.
-
(1997)
Pflügers Arch
, vol.434
, pp. 484-491
-
-
Weinreich, F.1
Wood, P.G.2
Riordan, J.R.3
Nagel, G.4
-
37
-
-
2542500548
-
Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes
-
Yan W, Samaha FF, Ramkumar M, Kleyman TR, Rubenstein RC. Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes. J Biol Chem 279: 23183-23192, 2004.
-
(2004)
J Biol Chem
, vol.279
, pp. 23183-23192
-
-
Yan, W.1
Samaha, F.F.2
Ramkumar, M.3
Kleyman, T.R.4
Rubenstein, R.C.5
-
38
-
-
33644856674
-
Differential modulation of a polymorphism in the COOH terminus of the α-subunit of the human epithelial sodium channel by protein kinase Cdelta
-
Yan W, Suaud L, Kleyman TR, Rubenstein RC. Differential modulation of a polymorphism in the COOH terminus of the α-subunit of the human epithelial sodium channel by protein kinase Cdelta. Am J Physiol Renal Physiol 290: F279-F288, 2006.
-
(2006)
Am J Physiol Renal Physiol
, vol.290
-
-
Yan, W.1
Suaud, L.2
Kleyman, T.R.3
Rubenstein, R.C.4
|