-
1
-
-
0029616734
-
Cystic fibrosis: Genotypic and phenotypic variations
-
Zielenski, J., and Tsui, L. C. (1995) Cystic fibrosis: genotypic and phenotypic variations. Annu. Rev. Genet. 2, 777-807
-
(1995)
Annu. Rev. Genet.
, vol.2
, pp. 777-807
-
-
Zielenski, J.1
Tsui, L.C.2
-
2
-
-
33645130994
-
Cystic fibrosis since 1938
-
Davis, P. B. (2006) Cystic fibrosis since 1938. Am. J. Crit. Care Med. 173, 475-482
-
(2006)
Am. J. Crit. Care Med.
, vol.173
, pp. 475-482
-
-
Davis, P.B.1
-
3
-
-
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
-
4
-
-
0025987020
-
Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel
-
Cheng, S. H., Rich, D. P., Marshall, J., Gregory, R. J., Welsh, M. J., and Smith, A. E. (1991) Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel. Cell 66, 1027-1036
-
(1991)
Cell
, vol.66
, pp. 1027-1036
-
-
Cheng, S.H.1
Rich, D.P.2
Marshall, J.3
Gregory, R.J.4
Welsh, M.J.5
Smith, A.E.6
-
5
-
-
84888085224
-
Regulatory R region of the CFTR chloride channel is a dynamic integrator of phospho-dependent intra- and intermolecular interactions
-
Bozoky, Z., Krzeminski, M., Muhandiram, R., Birtley, J. R., Al-Zahrani, A., Thomas, P. J., Frizzell, R. A., Ford, R. C., and Forman-Kay, J. D. (2013) Regulatory R region of the CFTR chloride channel is a dynamic integrator of phospho-dependent intra- and intermolecular interactions. Proc. Natl. Acad. Sci. U. S. A. 110, E4427-4436
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. E4427-E4436
-
-
Bozoky, Z.1
Krzeminski, M.2
Muhandiram, R.3
Birtley, J.R.4
Al-Zahrani, A.5
Thomas, P.J.6
Frizzell, R.A.7
Ford, R.C.8
Forman-Kay, J.D.9
-
6
-
-
75749153312
-
Strict coupling between CFTR's catalytic cycle and gating of its Cl-ion pore revealed by distributions of open channel burst durations
-
Csanády, L., Vergani, P., and Gadsby, D. C. (2010) Strict coupling between CFTR's catalytic cycle and gating of its Cl-ion pore revealed by distributions of open channel burst durations. Proc. Natl. Acad. Sci. U. S. A. 107, 1241-1246
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 1241-1246
-
-
Csanády, L.1
Vergani, P.2
Gadsby, D.C.3
-
7
-
-
0141513675
-
Prolonged nonhydrolytic interaction of nucleotide with CFTR's NH2-terminal nucleotide binding domain and its role inchannel gating
-
Basso, C., Vergani, P., Nairn, A. C., and Gadsby, D. C. (2003) Prolonged nonhydrolytic interaction of nucleotide with CFTR's NH2-terminal nucleotide binding domain and its role inchannel gating. J. Gen. Physiol. 122, 333-348
-
(2003)
J. Gen. Physiol.
, vol.122
, pp. 333-348
-
-
Basso, C.1
Vergani, P.2
Nairn, A.C.3
Gadsby, D.C.4
-
8
-
-
0037013262
-
The first nucleotide binding domain of cystic fibrosis transmembrane conductance regulator is a site of stable nucleotide interaction, whereas the second is a site of rapid turnover
-
Aleksandrov, L., Aleksandrov, A. A., Chang, X. B., and Riordan, J. R. (2002) The First Nucleotide Binding Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is a Site of Stable Nucleotide Interaction, whereas the Second Is a Site of Rapid Turnover. J. Biol. Chem. 277, 15419-15425
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 15419-15425
-
-
Aleksandrov, L.1
Aleksandrov, A.A.2
Chang, X.B.3
Riordan, J.R.4
-
9
-
-
33749039521
-
The two ATP binding sites of cystic fibrosis transmembrane conductance regulator (CFTR) play distinct roles in gating kinetics and energetics
-
Zhou, Z., Wang, X., Liu, H. Y., Zou, X., Li, M., and Hwang, T. C. (2006) The two ATP binding sites of cystic fibrosis transmembrane conductance regulator (CFTR) play distinct roles in gating kinetics and energetics. J. Gen. Physiol. 128, 413-422
-
(2006)
J. Gen. Physiol.
, vol.128
, pp. 413-422
-
-
Zhou, Z.1
Wang, X.2
Liu, H.Y.3
Zou, X.4
Li, M.5
Hwang, T.C.6
-
10
-
-
33750222000
-
In vivo phosphorylation of CFTR promotes formation of a nucleotide binding domain heterodimer
-
Mense, M., Vergani, P., White, D. M., Altberg, G., Nairn, A. C., and Gadsby, D. C. (2006) In vivo phosphorylation of CFTR promotes formation of a nucleotide binding domain heterodimer. EMBO J. 25, 4728-4739
-
(2006)
EMBO J.
, vol.25
, pp. 4728-4739
-
-
Mense, M.1
Vergani, P.2
White, D.M.3
Altberg, G.4
Nairn, A.C.5
Gadsby, D.C.6
-
11
-
-
42649118768
-
Computational studies reveal phosphorylation-dependent changes in the unstructured R domain of CFTR
-
Hegedüs, T., Serohijos, A. W., Dokholyan, N. V., He, L., and Riordan, J. R. (2008) Computational studies reveal phosphorylation-dependent changes in the unstructured R domain of CFTR. J. Mol. Biol. 37, 1052-1063
-
(2008)
J. Mol. Biol.
, vol.37
, pp. 1052-1063
-
-
Hegedüs, T.1
Serohijos, A.W.2
Dokholyan, N.V.3
He, L.4
Riordan, J.R.5
-
12
-
-
77649256457
-
ATP-independent CFTR channel gating and allosteric modulation by phosphorylation
-
Wang, W., Wu, J., Bernard, K., Li, G., Wang, G., Bevensee, M. O., and Kirk, K. L. (2010) ATP-independent CFTR channel gating and allosteric modulation by phosphorylation. Proc. Natl. Acad. Sci. U. S. A. 107, 3888-3893
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 3888-3893
-
-
Wang, W.1
Wu, J.2
Bernard, K.3
Li, G.4
Wang, G.5
Bevensee, M.O.6
Kirk, K.L.7
-
13
-
-
0026621245
-
ABC transporters: From microorganisms to man
-
Higgins, C. F. (1992) ABC transporters: from microorganisms to man. Annu. Rev. Cell Biol. 8, 67-113
-
(1992)
Annu. Rev. Cell Biol.
, vol.8
, pp. 67-113
-
-
Higgins, C.F.1
-
14
-
-
61449341855
-
Review. Structure and mechanism of ATP-binding cassette transporters
-
Locher, K. P. (2009) Review. Structure and mechanism of ATP-binding cassette transporters. Philos. Trans. R. Soc. Lond. B Biol. Sci. 364, 239-245
-
(2009)
Philos. Trans. R. Soc. Lond. B Biol. Sci.
, vol.364
, pp. 239-245
-
-
Locher, K.P.1
-
15
-
-
33846684215
-
CFTR (ABCC7) is a hydrolyzable-ligand-gated channel
-
Aleksandrov, A. A., Aleksandrov, L. A., and Riordan, J. R. (2007) CFTR (ABCC7) is a hydrolyzable-ligand-gated channel. Pflugers Arch. 453, 693-702
-
(2007)
Pflugers Arch.
, vol.453
, pp. 693-702
-
-
Aleksandrov, A.A.1
Aleksandrov, L.A.2
Riordan, J.R.3
-
16
-
-
79953853890
-
A unified view of cystic fibrosis transmembrane conductance regulator (CFTR) gating: Combining the allosterism of a ligand-gated channel with the enzymatic activity of an ATP-binding cassette (ABC) transporter
-
Kirk, K. L., and Wang, W. (2011) A unified view of cystic fibrosis transmembrane conductance regulator (CFTR) gating: combining the allosterism of a ligand-gated channel with the enzymatic activity of an ATP-binding cassette (ABC) transporter. J. Biol. Chem. 286, 12813-12819
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 12813-12819
-
-
Kirk, K.L.1
Wang, W.2
-
17
-
-
33847134349
-
Structure of the multidrug ABC transporter Sav1866 from Staphylococcus aureus in complex with AMP-PNP
-
Dawson, R. J., and Locher, K. P. (2007) Structure of the multidrug ABC transporter Sav1866 from Staphylococcus aureus in complex with AMP-PNP. FEBS Lett. 581, 935-938
-
(2007)
FEBS Lett.
, vol.581
, pp. 935-938
-
-
Dawson, R.J.1
Locher, K.P.2
-
18
-
-
37649004412
-
Flexibility in the ABC transporter MsbA: Alternating access with a twist
-
Ward, A., Reyes, C. L., Yu, J., Roth, C. B., and Chang, G. (2007) Flexibility in the ABC transporter MsbA: Alternating access with a twist. Proc. Natl. Acad. Sci. U. S. A. 104, 19005-19010
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 19005-19010
-
-
Ward, A.1
Reyes, C.L.2
Yu, J.3
Roth, C.B.4
Chang, G.5
-
19
-
-
67349185408
-
Ion channels versus ion pumps: The principal difference, in principle
-
Gadsby, D. C. (2009) Ion channels versus ion pumps: the principal difference, in principle. Nat. Rev. Mol. Cell Biol. 10, 344-352
-
(2009)
Nat. Rev. Mol. Cell Biol.
, vol.10
, pp. 344-352
-
-
Gadsby, D.C.1
-
20
-
-
42149120706
-
Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function
-
Serohijos, A. W., Hegedus, T., Aleksandrov, A. A., He, L., Cui, L., Dokholyan, N. V., and Riordan J. R. (2008) Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function. Proc. Natl. Acad. Sci. U. S. A. 105, 3256-3261
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 3256-3261
-
-
Serohijos, A.W.1
Hegedus, T.2
Aleksandrov, A.A.3
He, L.4
Cui, L.5
Dokholyan, N.V.6
Riordan, J.R.7
-
21
-
-
70349847830
-
Molecular models of the open and closed states of the whole human CFTR protein
-
Mornon, J. P., Lehn, P., and Callebaut, I. (2009) Molecular models of the open and closed states of the whole human CFTR protein. Cell Mol. Life Sci. 66, 3469-3486
-
(2009)
Cell Mol. Life Sci.
, vol.66
, pp. 3469-3486
-
-
Mornon, J.P.1
Lehn, P.2
Callebaut, I.3
-
22
-
-
84858633600
-
Cystic fibrosis transmembrane conductance regulator: A molecular model defines the architecture of the anion conduction path and locates a "bottleneck" in the pore
-
Norimatsu, Y., Ivetac, A., Alexander, C., Kirkham, J., O'Donnell, N., Dawson, D. C., and Sansom, M. S. (2012) Cystic fibrosis transmembrane conductance regulator: a molecular model defines the architecture of the anion conduction path and locates a "bottleneck" in the pore. Biochemistry 51, 2199-2212
-
(2012)
Biochemistry
, vol.51
, pp. 2199-2212
-
-
Norimatsu, Y.1
Ivetac, A.2
Alexander, C.3
Kirkham, J.4
O'Donnell, N.5
Dawson, D.C.6
Sansom, M.S.7
-
23
-
-
84864258150
-
New model of cystic fibrosis transmembrane conductance regulator proposes active channel-like conformation
-
Dalton, J., Kalid, O., Schushan, M., Ben-Tal, N., and Villà-Freixa, J. (2012) New model of cystic fibrosis transmembrane conductance regulator proposes active channel-like conformation. J. Chem. Inf. Model. 52, 1842-1853
-
(2012)
J. Chem. Inf. Model.
, vol.52
, pp. 1842-1853
-
-
Dalton, J.1
Kalid, O.2
Schushan, M.3
Ben-Tal, N.4
Villà-Freixa, J.5
-
24
-
-
84884699027
-
Modeling the conformational changes underlying channel opening in CFTR
-
Rahman, K. S., Cui, G., Harvey, S. C., and McCarty N. A. (2013) Modeling the conformational changes underlying channel opening in CFTR. PLoS One 8, e74574
-
(2013)
PLoS One
, vol.8
, pp. e74574
-
-
Rahman, K.S.1
Cui, G.2
Harvey, S.C.3
McCarty, N.A.4
-
25
-
-
77449137874
-
The conformational transition pathway of ATP binding cassette transporter MsbA revealed by atomistic simulations
-
Weng, J-W., Fan, K-N., and Wang, W-N. (2010) The conformational transition pathway of ATP binding cassette transporter MsbA revealed by atomistic simulations. J. Biol. Chem. 285, 3053-3063
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 3053-3063
-
-
Weng, J.-W.1
Fan, K.-N.2
Wang, W.-N.3
-
26
-
-
84874891985
-
Molecular disruption of the power stroke in the ATP-binding cassette transport protein MsbA
-
Doshi, R., Ali, A., Shi, W., Freeman, E. V., Fagg, L. A., and van Veen, H. W. (2013) Molecular disruption of the power stroke in the ATP-binding cassette transport protein MsbA. J. Biol. Chem. 288, 6801-6813
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 6801-6813
-
-
Doshi, R.1
Ali, A.2
Shi, W.3
Freeman, E.V.4
Fagg, L.A.5
Van Veen, H.W.6
-
27
-
-
84888050424
-
CFTR: Effect of ICL2 and ICL4 amino acids in close proximity on the current properties of the channel
-
Billet, A., Mornon, J-P., Jollivet, M., Lehn, P., Callebaut, I., Becq, F. (2013) CFTR: Effect of ICL2 and ICL4 amino acids in close proximity on the current properties of the channel. J. Cystic Fibrosis 12, 737-745
-
(2013)
J. Cystic Fibrosis
, vol.12
, pp. 737-745
-
-
Billet, A.1
Mornon, J.-P.2
Jollivet, M.3
Lehn, P.4
Callebaut, I.5
Becq, F.6
-
28
-
-
21244494942
-
Activating cystic fibrosis transmembrane conductance regulator channels with pore blocker analogs
-
Wang, W., Li, G., Clancy, J. P., and Kirk, K. L. (2005) Activating cystic fibrosis transmembrane conductance regulator channels with pore blocker analogs. J. Biol. Chem. 280, 23622-23630
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 23622-23630
-
-
Wang, W.1
Li, G.2
Clancy, J.P.3
Kirk, K.L.4
-
29
-
-
0032522433
-
Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel
-
Mathews, C. J., Tabcharani, J. A., Chang, X. B., Jensen, T. J., Riordan, J. R., and Hanrahan, J. W. (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
-
(1998)
J. Physiol.
, vol.508
, pp. 365-377
-
-
Mathews, C.J.1
Tabcharani, J.A.2
Chang, X.B.3
Jensen, T.J.4
Riordan, J.R.5
Hanrahan, J.W.6
-
30
-
-
0029878720
-
VMD: Visual molecular dynamics
-
Humphrey, W., Dalke, A., and Schulten, K. (1996) VMD: visual molecular dynamics. J. Mol. Graph. 14, 33-38
-
(1996)
J. Mol. Graph.
, vol.14
, pp. 33-38
-
-
Humphrey, W.1
Dalke, A.2
Schulten, K.3
-
31
-
-
84865723813
-
Optimization of the additive CHARMM all-atom protein force field targeting improved sampling of the backbone phi, psi and sidechain chi (1) and chi (2) dihedral angles
-
Best, R. B., Zhu, X., Shim, J., Lopes, P. E., Mittal, J., Feig, M., and Mackerell, A. D., Jr. (2012) Optimization of the additive CHARMM all-atom protein force field targeting improved sampling of the backbone phi, psi and sidechain chi (1) and chi (2) dihedral angles. J. Chem. Theory Comput. 8, 3257-3273
-
(2012)
J. Chem. Theory Comput.
, vol.8
, pp. 3257-3273
-
-
Best, R.B.1
Zhu, X.2
Shim, J.3
Lopes, P.E.4
Mittal, J.5
Feig, M.6
Mackerell, A.D.7
-
32
-
-
0035964342
-
Electrostatics of nanosystems: Application to microtubules and the ribosome
-
Baker, N. A., Sept, D., Joseph, S., Holst, M. J., and McCammon, J. A. (2001) Electrostatics of nanosystems: application to microtubules and the ribosome. Proc. Natl. Acad. Sci. U. S. A. 98, 10037-10041
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 10037-10041
-
-
Baker, N.A.1
Sept, D.2
Joseph, S.3
Holst, M.J.4
McCammon, J.A.5
-
33
-
-
0036896008
-
Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion
-
Ma, T., Thiagarajah, J. R., Yang, H., Sonawane, N. D., Folli, C., Galietta, L. J., and Verkman, A. S. (2002) Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion. J. Clin. Invest. 110, 1651-1658
-
(2002)
J. Clin. Invest.
, vol.110
, pp. 1651-1658
-
-
Ma, T.1
Thiagarajah, J.R.2
Yang, H.3
Sonawane, N.D.4
Folli, C.5
Galietta, L.J.6
Verkman, A.S.7
-
34
-
-
73249114731
-
Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770
-
Van Goor, F., Hadida, S., Grootenhuis, P. D., Burton, B., Cao, D., Neuberger, T., Turnbull, A., Singh, A., Joubran, J., Hazlewood, A., Zhou, J., McCartney, J., Arumugam, V., Decker, C., Yang, J., Young, C., Olson, E. R., Wine, J. J., Frizzell, R. A., Ashlock, M., and Negulescu, P. (2009) Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770. Proc. Natl. Acad. Sci. U. S. A. 106, 18825-18830
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 18825-18830
-
-
Van Goor, F.1
Hadida, S.2
Grootenhuis, P.D.3
Burton, B.4
Cao, D.5
Neuberger, T.6
Turnbull, A.7
Singh, A.8
Joubran, J.9
Hazlewood, A.10
Zhou, J.11
McCartney, J.12
Arumugam, V.13
Decker, C.14
Yang, J.15
Young, C.16
Olson, E.R.17
Wine, J.J.18
Frizzell, R.A.19
Ashlock, M.20
Negulescu, P.21
more..
-
35
-
-
80455162465
-
A CFTR potentiatorinpatients with cystic fibrosis and the G551D mutation
-
Ramsey, B. W., Davies, J., McElvaney, N. G., Tullis, E., Bell, S. C., Dřevinek, P., Griese, M., McKone, E. F., Wainwright, C. E., Konstan, M. W., Moss, R., Ratjen, F., Sermet-Gaudelus, I., Rowe, S. M., Dong, Q., Rodriguez, S., Yen, K., Ordoñez, C., Elborn, J. S., VX08-770-102 Study Group. (2011) A CFTR potentiatorinpatients with cystic fibrosis and the G551D mutation. N. Engl. J. Med. 365, 1663-1672
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 1663-1672
-
-
Ramsey, B.W.1
Davies, J.2
McElvaney, N.G.3
Tullis, E.4
Bell, S.C.5
Dřevinek, P.6
Griese, M.7
McKone, E.F.8
Wainwright, C.E.9
Konstan, M.W.10
Moss, R.11
Ratjen, F.12
Sermet-Gaudelus, I.13
Rowe, S.M.14
Dong, Q.15
Rodriguez, S.16
Yen, K.17
Ordoñez, C.18
Elborn, J.S.19
-
36
-
-
0035886655
-
A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating
-
Fu, J., Ji, H. L., Naren, A. P., and Kirk, K. L. (2001) A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating. J. Physiol. 536, 459-470
-
(2001)
J. Physiol.
, vol.536
, pp. 459-470
-
-
Fu, J.1
Ji, H.L.2
Naren, A.P.3
Kirk, K.L.4
-
37
-
-
0028340159
-
Regulation of the gating of cystic fibrosis transmembrane conductance regulator Cl channels by phosphorylation and ATP hydrolysis
-
Hwang, T. C., Nagel, G., Nairn, A. C., and Gadsby, D. C. (1994) Regulation of the gating of cystic fibrosis transmembrane conductance regulator Cl channels by phosphorylation and ATP hydrolysis. Proc. Natl. Acad. Sci. U. S. A. 91, 4698-4702
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 4698-4702
-
-
Hwang, T.C.1
Nagel, G.2
Nairn, A.C.3
Gadsby, D.C.4
-
38
-
-
0036521974
-
Mutation of Walker-A lysine 464 in cystic fibrosis conductance regulator reveals functional interaction between its nucleotide-binding domains
-
Powe, A. C., Jr., Al-Nakkash, L., Li, M., and Hwang, T. C. (2002) Mutation of Walker-A lysine 464 in cystic fibrosis conductance regulator reveals functional interaction between its nucleotide-binding domains. J. Physiol. 539, 333-346
-
(2002)
J. Physiol.
, vol.539
, pp. 333-346
-
-
Powe, A.C.1
Al-Nakkash, L.2
Li, M.3
Hwang, T.C.4
-
40
-
-
79957820118
-
The most common cystic fibrosis-associated mutation destabilizes the dimeric state of the nucleotide-binding domains of CFTR
-
Jih, K. Y., Li, M., Hwang, T. C, and Bompadre, S. G. (2011) The most common cystic fibrosis-associated mutation destabilizes the dimeric state of the nucleotide-binding domains of CFTR. J. Physiol. 589, 2719-2731
-
(2011)
J. Physiol.
, vol.589
, pp. 2719-2731
-
-
Jih, K.Y.1
Li, M.2
Hwang, T.C.3
Bompadre, S.G.4
-
41
-
-
77649161249
-
Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore
-
Zhou, J. J., Li, M. S., Qi, J., and Linsdell, P. (2010) Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore. J Gen. Physiol. 135, 229-245
-
(2010)
J Gen. Physiol.
, vol.135
, pp. 229-245
-
-
Zhou, J.J.1
Li, M.S.2
Qi, J.3
Linsdell, P.4
-
42
-
-
84893069291
-
Catalyst-like modulation of transition states for CFTR channel opening and closing: New stimulation strategy exploits nonequilibrium gating
-
Csanády, L., and Töröcsik, B. (2014) Catalyst-like modulation of transition states for CFTR channel opening and closing: New stimulation strategy exploits nonequilibrium gating. J. Gen. Physiol. 143, 269-287
-
(2014)
J. Gen. Physiol.
, vol.143
, pp. 269-287
-
-
Csanády, L.1
Töröcsik, B.2
-
43
-
-
17544374096
-
Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity
-
Seibert, F. S., Linsdell, P., Loo, T. W., Hanrahan, J. W., Clarke, D. M., and Riordan, J. R. (1996) Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity. J. Biol. Chem. 271, 15139-15145
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 15139-15145
-
-
Seibert, F.S.1
Linsdell, P.2
Loo, T.W.3
Hanrahan, J.W.4
Clarke, D.M.5
Riordan, J.R.6
-
44
-
-
0035937443
-
Two-state allosteric behavior in a single-domain signaling protein
-
Volkman, B. F., Lipson, D., Wemmer, D. E., and Kern, D. (2001) Two-state allosteric behavior in a single-domain signaling protein. Science 291, 2429-2433
-
(2001)
Science
, vol.291
, pp. 2429-2433
-
-
Volkman, B.F.1
Lipson, D.2
Wemmer, D.E.3
Kern, D.4
-
46
-
-
84884239140
-
Allosteric coupling between the intracellular coupling helix 4 and regulatory sites of the first nucleotide-binding domain of CFTR
-
Dawson, J. E., Farber, P. J., and Forman-Kay, J. D. (2013) Allosteric coupling between the intracellular coupling helix 4 and regulatory sites of the first nucleotide-binding domain of CFTR. PLoS One 8, e74347
-
(2013)
PLoS One
, vol.8
, pp. e74347
-
-
Dawson, J.E.1
Farber, P.J.2
Forman-Kay, J.D.3
-
47
-
-
84879066653
-
Converting nonhydrolyzable nucleotides to strong cystic fibrosis transmembrane conductance regulator (CFTR) agonists by gain of function (GOF) mutations
-
Okeyo, G., Wang, W., Wei, S., and Kirk, K. L. (2013) Converting nonhydrolyzable nucleotides to strong cystic fibrosis transmembrane conductance regulator (CFTR) agonists by gain of function (GOF) mutations. J. Biol. Chem. 288, 17122-17133
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 17122-17133
-
-
Okeyo, G.1
Wang, W.2
Wei, S.3
Kirk, K.L.4
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